Evaluation/staging of pelvic organ prolapse.
\r\n\tgas sensors.
",isbn:"978-1-80356-963-5",printIsbn:"978-1-80356-962-8",pdfIsbn:"978-1-80356-964-2",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!0,isSalesforceBook:!1,isNomenclature:!1,hash:"8eeb7ab232fa8d5c723b61e0da251857",bookSignature:"Dr. Soumen Dhara and Dr. Gorachand Dutta",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/11513.jpg",keywords:"Fabrication Technologies, Applications, Characterizations, Case Studies, Various Gas Sensors, Improvement of Lifestyle, Societal Benefit, Bio-Sensors, Bioreceptor Molecules, Integration, Packaging, Lab-on-Chip",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"April 8th 2022",dateEndSecondStepPublish:"June 17th 2022",dateEndThirdStepPublish:"August 16th 2022",dateEndFourthStepPublish:"November 4th 2022",dateEndFifthStepPublish:"January 3rd 2023",dateConfirmationOfParticipation:null,remainingDaysToSecondStep:"2 months",secondStepPassed:!0,areRegistrationsClosed:!1,currentStepOfPublishingProcess:4,editedByType:null,kuFlag:!1,biosketch:"A pioneering researcher in nanowire heterostructures and laser spectroscopy, recipient of JSPS (Govt. of Japan) and NPDF (Govt. of India) fellowships, and member of MRS(USA), MRS(India), IPA(India).",coeditorOneBiosketch:"Assistant Professor with the School of Medical Science and Technology, Indian Institute of Technology Kharagpur with research interests that include the design and characterization of portable biosensors, biodevices, and sensor interfaces for miniaturized systems and biomedical applications for point-of-care testing.",coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"196334",title:"Dr.",name:"Soumen",middleName:null,surname:"Dhara",slug:"soumen-dhara",fullName:"Soumen Dhara",profilePictureURL:"https://mts.intechopen.com/storage/users/196334/images/system/196334.jpeg",biography:"Dr. Dhara received his Ph. D in Physics in 2012 from Indian Institute of Technology Guwahati, India. Presently, he is associated with the Faculty of Science, Sri Sri University, India as an Assistant Professor in Physics. Prior to joining the current\naffiliation, he was a postdoctoral fellow at different renowned institutions, Kobe University Japan, S. N. Bose National Centre for Basic Sciences, India and Cardiff University, United Kingdom. He was awarded prestigious JSPS postdoctoral fellowship based on his research contribution on semiconducting nanowires. He has published more than 32 research articles including 1 review article in high profile international journals and 3 book chapters to his credit. His research trust areas of interests are semiconductor nanostructures, optoelectronics, solid state lighting and light sensors, spectroscopy of nanomaterials, thin-film transistors (TFTs) etc.",institutionString:"Sri Sri University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"Sri Sri University",institutionURL:null,country:{name:"India"}}}],coeditorOne:{id:"442408",title:"Dr.",name:"Gorachand",middleName:null,surname:"Dutta",slug:"gorachand-dutta",fullName:"Gorachand Dutta",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:"Dr. Gorachand Dutta, PhD is an Assistant Professor with the School of MedicalScience and Technology, Indian Institute of Technology Kharagpur. His research interests include the design and characterization of portable\r\nbiosensors, biodevices and sensor interfaces for miniaturized systems and biomedical applications for point-of-care testing. He received his Ph.D in Biosensor and Electrochemistry from Pusan National University, South Korea,\r\nwhere he developed different class of electrochemical sensors and studied the electrochemical properties of gold, platinum, and palladium based metal electrodes. He completed his Post-doctoral fellowships in the Department of\r\nMechanical Engineering, Michigan State University, USA and Department of Electronic and Electrical Engineering at University of Bath, UK. He has expertise on label-free multichannel electrochemical biosensors, electronically\r\naddressable biosensor arrays, aptamer- and DNA-based sensors and surface bio-functionalization.",institutionString:"Indian Institute of Technology Kharagpur",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"0",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"Indian Institute of Technology Kharagpur",institutionURL:null,country:{name:"India"}}},coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"11",title:"Engineering",slug:"engineering"}],chapters:null,productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},personalPublishingAssistant:{id:"429341",firstName:"Paula",lastName:"Gavran",middleName:null,title:"Ms.",imageUrl:"//cdnintech.com/web/frontend/www/assets/author.svg",email:"paula@intechopen.com",biography:null}},relatedBooks:[{type:"book",id:"10198",title:"Response Surface Methodology in Engineering Science",subtitle:null,isOpenForSubmission:!1,hash:"1942bec30d40572f519327ca7a6d7aae",slug:"response-surface-methodology-in-engineering-science",bookSignature:"Palanikumar Kayaroganam",coverURL:"https://cdn.intechopen.com/books/images_new/10198.jpg",editedByType:"Edited by",editors:[{id:"321730",title:"Prof.",name:"Palanikumar",surname:"Kayaroganam",slug:"palanikumar-kayaroganam",fullName:"Palanikumar Kayaroganam"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"1591",title:"Infrared Spectroscopy",subtitle:"Materials Science, Engineering and Technology",isOpenForSubmission:!1,hash:"99b4b7b71a8caeb693ed762b40b017f4",slug:"infrared-spectroscopy-materials-science-engineering-and-technology",bookSignature:"Theophile Theophanides",coverURL:"https://cdn.intechopen.com/books/images_new/1591.jpg",editedByType:"Edited by",editors:[{id:"37194",title:"Dr.",name:"Theophile",surname:"Theophanides",slug:"theophile-theophanides",fullName:"Theophile Theophanides"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3161",title:"Frontiers in Guided Wave Optics and Optoelectronics",subtitle:null,isOpenForSubmission:!1,hash:"deb44e9c99f82bbce1083abea743146c",slug:"frontiers-in-guided-wave-optics-and-optoelectronics",bookSignature:"Bishnu Pal",coverURL:"https://cdn.intechopen.com/books/images_new/3161.jpg",editedByType:"Edited by",editors:[{id:"4782",title:"Prof.",name:"Bishnu",surname:"Pal",slug:"bishnu-pal",fullName:"Bishnu Pal"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"371",title:"Abiotic Stress in Plants",subtitle:"Mechanisms and Adaptations",isOpenForSubmission:!1,hash:"588466f487e307619849d72389178a74",slug:"abiotic-stress-in-plants-mechanisms-and-adaptations",bookSignature:"Arun Shanker and B. 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Many women with prolapse experience symptoms that impact daily activities, sexual function, and exercise. The presence of POP can have a detrimental impact on body image and sexuality. Pelvic organ prolapse is an increasingly common condition seen with aging population with a prevalence of 41–50% of women above 40 years. The annual incidence of surgery for POP is within the range of 15–49 cases per 10,000 women years [1]. Pelvic floor defects result from attenuation of the supportive structures or by neuromuscular dysfunction due to obstetric trauma. Pregnancy itself, without vaginal birth, has been cited as a risk factor as well. Genital atrophy and hypoestrogenism also play important contributory roles in the pathogenesis of prolapse. However, the exact mechanisms are not completely understood. Prolapse may potentially result from pelvic tumors, sacral nerve disorders, and diabetic neuropathy [2].
\nOlder terms describing pelvic organ prolapse (e.g., cystocele, urethrocele, rectocele) have been replaced because they do not provide complete information regarding the structures on the other side of the vaginal bulge, especially in women who have had previous pelvic organ prolapse surgery.
\nPresently, the pelvis is divided into anterior, posterior, and middle or apical compartments. Following hysterectomy, prolapse of the vaginal apex with or without prolapse of the anterior and/or posterior vaginal wall is referred to as vault prolapse [2, 3].
\nPelvic organ support is maintained by complex interactions between the vagina, levator ani muscle, and pelvic floor connective tissue. A system of three integrated levels of vaginal support has been described by De Lancey [1].
Level 1: The cardinal uterosacral ligament complex.
Level 2: Midvaginal supports—pubocervical and rectovaginal fascia.
Level 3: Urogenital diaphragm and the perineal body.
The prolapse is usually described according to the area of the vagina in which it occurs. Assumptions are often made about which organ is behind the vaginal wall that is prolapsing.
\nAnatomical classification according to vaginal wall:
Anterior: cystocele (bladder most common) and urethrocele (urethra).
Middle: vault of the uterus (after hysterectomy).
Posterior: rectocele (rectum) and enterocele (small bowel, omentum).
\n
Anterior wall
Upper 2/3 cystocele
Lower 1/3 urethrocele
Posterior wall
Upper 1/3 enterocele
Middle 1/3 rectocele
Lower 1/3 deficient perineum
Uterine prolapse
Grade 0: Normal position
Grade 1: Descent into vagina not reaching the introitus
Grade 2: Descent up to the introitus
Grade 3: Descent outside the introitus
Grade 4: Procidentia [2]
Uterovaginal prolapse usually occurs in nulliparous prolapse due to congenital weakness of cervical ligaments.
Vaginouterine prolapse usually occurs in cases of prolapse resulting from obstetrical trauma.
Pelvic organ prolapse quantification system refers to an objective, site-specific system for describing, quantifying, and staging pelvic support in women (Figure 1). It provides a standardized tool for documenting, comparing, and communicating clinical findings with proven interobserver and intraobserver reliability. The POP-Q system gained the attention of the specialists all over the world, being approved by the International Continence Society (ICS), the American Urogynecologic Society (AUGS), and the Society of Gynecologic Surgeons for the description of female pelvic organ prolapse. It is the most common system used by gynecologists and urogynecologists, although other systems have been devised (Figures 2–9) [4].
\nPOP-Q points. Aa, anterior vaginal wall 3 cm proximal to the urethral meatus (−3 cm to +3 cm); Ba,most distal position of the remaining upper anterior vaginal wall (−3 cm to +tvl); C, most distal edge of cervix or vaginal cuff scar; D, posterior fornix (n/a if posthysterectomy); Ap, posterior vaginal wall 3 cm proximal to the hymen (−3 cm to +3 cm); Bp, most distal position of the remaining upper posterior vaginal wall (−3 cm to + tvl); genital hiatus (gh), measured from the middle of external urethral meatus to the posterior midline hymen; perineal body (pb), measured from the posterior margin of gh to the middle of anal opening; total vaginal length (tvl), depth of the vagina when point D or C is reduced to normal position.
Point Aa being measured by graded spatula.
Point Ba being measured by graded spatula.
Point C.
Point Ap.
Point Bp.
Point D.
Genital hiatus (gh).
Perineal body (Pb).
The POP-Q may be an easier classification system to use in routine clinical practice. It was developed by the International Urogynecological Association to provide a less cumbersome exam tool [4]. The POP-Q stages (Table 1) prolapse for the anterior and posterior vaginal walls, the apex/cuff of the vagina and the cervix. For women posthysterectomy, there are three stages; for women with an intact uterus, there are four. The exam is carried out similarly to the standard POP-Q exam, with a half speculum placed in the vagina to visualize the vaginal walls and cervix.
\nPelvic organ prolapse quantification system | |
---|---|
Stage | Description |
0 | No prolapse |
I | >1 cm above the hymen |
II | ≤1 cm proximal or distal to the plane of the hymen |
III | >1 cm below the plane of the hymen, but protrudes no farther than 2 cm less than the total vaginal length |
IV | Eversion of the lower genital tract is complete |
Evaluation/staging of pelvic organ prolapse.
POP-Q staging criteria.
Stage 0: Aa, Ap, Ba, Bp = −3 cm and C or D ≤ − (tvl − 2) cm.
Stage l: Stage 0 criteria not met and leading edge < −1 cm.
Stage ll: Leading edge ≥ −1 cm but ≤ +1 cm.
Stage lll: Leading edge > +1 cm but < + (tvl − 2) cm.
Stage lV: Leading edge ≥ + (tvl −2) cm [3, 4].
A disadvantage of POP-Q is that all points and measures are taken in the midline; as a consequence, the POP-Q does not reflect asymmetries and cannot be used to describe, for example, paravaginal defects. One has also to keep in mind that the POP-Q depends on the cooperation of the patient and to the strength of her cough or Valsalva maneuver; it is therefore unreasonable to assume that in an individual patient, the POP-Q will always be identical [4].
\nMost patients with pelvic organ prolapse are asymptomatic. Seeing or feeling a bulge of tissue that protrudes to or past the vaginal opening is the most specific symptom.
\nDuring a well-woman examination, she should be asked regarding any obvious bulge seen or felt in vagina. The report of a bulge has an 81% positive predictive value and a 76% negative predictive value for pelvic organ prolapse.
\nPatient may complain of an increase in bulging and discomfort with progression of day [1]. Extensive standing, lifting, coughing, and physical exertion may increase patient awareness of discomfort in the pelvis, vagina, abdomen, and low back. Pelvic organ prolapse may progress with increasing body mass index. Weight loss does not reverse the prolapse.
\nVaginal discharge may be present in patients with complete uterine prolapse (i.e., procidentia) who have a decubitus ulcer of the cervix or vagina.
\nPatients may have difficulty urinating—stress incontinence affects 40% of patients with pelvic organ prolapse; therefore, they should be asked about frequency, urgency, and sensation of incomplete emptying of the bladder, because they may not volunteer such information. Urinary outlet obstruction may occur because of the pressure on the urethra in anterior vaginal prolapse and sometimes in large posterior vaginal prolapse. Screening is advocated for urinary tract infection, postvoid residual urine volume, and the presence or absence of bladder sensation.
\nSymptoms may not correlate with the location or severity of the prolapsed compartment.
\nPatients with posterior vaginal prolapse sometimes use manual pressure on the perineum or posterior vagina to help with defecation. These maneuvers are called “splinting.”
\nThough patients of prolapse attribute back and pelvic pain to their prolapse, very little evidence is available to show that this disorder causes pain, so other causes of pain should be ruled out.
\nSexual activity, body image, and quality of life may be affected [3].
\nAssessment will include weight, body mass index, and blood pressure, as well as assessment of any varicose veins or hypermobile joints, since these can be markers of a tendency to connective tissue laxity which predisposes to POP and, importantly, to recurrence after surgical repair [2].
\nOn examination of the abdomen, inspect for incisions of previous surgery (which may be associated with intra-abdominal adhesions affecting subsequent surgical approaches), and exclude masses or ascites. The presence of umbilical or other hernia can again indicate underlying connective tissue weakness and may require concomitant surgical correction [2, 3].
\nOn inspection of the vulva, note the presence of any atrophy and whether there is any ulceration of prolapsed tissues that may require local estrogen therapy before surgery. Wide genital hiatus with visible vaginal walls or midline asymmetry on Valsalva shows levator ani damage.
\nFor stress urinary incontinence, the patient needs to be examined with full bladder and asked to cough or strain, and leakage of urine confirms positive stress provocation test.
\nOn examination in lithotomy position, if there is visible vaginal bulge, look for vaginal wall rugosities which predict an intact fascial layer in the midline and a probable lateral defect, or if absent, it suggests a midline defect with only the skin and attenuated connective tissue present.
\nIn some mild cases of vaginal wall and uterine prolapse, examination of the patient in standing position is the only way to explore it.
\nMostly for demonstration of uterine prolapse. Either the uterus will be obviously protruded or protrude when the patient is asked to strain.
\nIn this position, the aim is to demonstrate the different types of vaginal wall prolapse. The patient is asked to lie on her left side at the edge of the table. The left leg is extended, while the right leg is flexed. Afterward, a sterile Sims’ speculum is inserted into the vagina gently first to expose the anterior vaginal wall. Then it is pulled backward gradually to expose the posterior vaginal wall. Cystocele and rectocele are usually diagnosed by this examination.
\nExamination with a Cusco’s bivalve speculum allows assessment of the cervix (including a Pap smear, if appropriate), but not of prolapse. The use of a Sims’ speculum is required to carefully assess the anterior and posterior compartments and to assess the supports of the cervix or the vault if there has been a previous hysterectomy. If prolapse is visible at the vaginal introitus or on Valsalva maneuver, a systematic examination should be performed. With the patient in a supine position, a suitable sized vaginal speculum is introduced in the vagina to view the cervix or vaginal cuff, and the extent to which the cervix or the vaginal vault follows the speculum through and out of the vagina is noted, and the speculum is slowly removed while performing Valsalva maneuver.
\nTo examine the anterior vaginal wall, the posterior vaginal wall is retracted with the fixed blade, and the extent of any anterior vaginal prolapse during the Valsalva maneuver is noted and vice versa to examine posterior vaginal wall. Any resulting prolapse is noted.
\nDecubitus ulcers are inspected and palpated. It is common to require sponge holding forceps to aid in support of the vaginal walls, as this can obscure the view.
\nBimanual examination is performed to check the uterine size and mobility, as well as to exclude unsuspected adnexal pathology, such as ovarian tumors. This also allows an assessment of vaginal muscle tone. Rectal examination may distinguish rectocele from enterocele. Make sure you ask the woman to direct your attention to any other findings that she has noted, that you have not discovered, or that she wants to draw your attention to.
\nBonney’s stress test is performed following reduction of prolapsed. If test is positive, incontinence surgery should be performed at the time of prolapse surgery. Testing for integrity of anal sphincter should be assessed for resting tone and voluntary squeeze and sensation around the vulva with the bulbocavernous reflex. (Stroking lateral to clitoris contraction of bilateral bulbocavernous muscle is observed.) The anocutaneous reflex (anal wink sign) is triggered by stroking the skin immediately surrounding the anus and observing a reflexive contraction of the external anal sphincter; this reflex should be elicited bilaterally. Absence of these reflexes is not always abnormal, and hyperreflexia or asymmetry may in fact be more suggestive of a neurologic etiology. Crude sensory testing is advocated for evidence of pudendal neuropathy [4, 5].
\nGrading pelvic floor muscle strength:
No discernible contraction.
Barely palpable, flickering contraction, not visible on inspection of the perineum.
Weak, distinctly palpable contraction, felt as slight pressure on the examining finger.
Moderate muscle strength, distinct pressure on the examining finger, palpable upward and forward movement, visible on the perineal surface.
Good muscle strength, elevation possible against slight resistance, circular pressure can be felt around the examining finger. During simultaneous examination by the index and middle finger, these are pressed against each other.
Very strong muscle strength, contraction possible against vigorous resistance, with suction-type effect on the examining finger. During simultaneous examination by the index and middle finger, these are pressed against each other despite resistance.
Digital examination makes it possible to distinguish between the left and right side of the levator ani. It is capable of quantifying strength, strength endurance, fast contraction, and fast contraction endurance for clinical purposes [2].
A full description of the examination is recorded, including the following:
Type of examination table, speculum, and retractors
Patient position
Bladder and rectal fullness
It is important to note and document any episodes of urinary, fecal, or flatal incontinence that occur during the examination. The findings of the examination should be recorded using a quantitative and reproducible method for recording POP such as the POP-Q , Baden-Walker, or Shaw systems [4, 5].
\nFurther studies depend on the symptoms, stage of prolapse, and treatment plan. If needed for definitive treatment planning, urodynamic studies can help in identifying those patients with lower urinary tract symptoms (urinary incontinence) who are most likely to get benefit from surgery or may require stress incontinence surgery. Patients with defecatory symptoms and/or fecal incontinence may need anal manometry and endoanal ultrasonography [5].
\nTaking a thorough history and performing a careful physical examination of women who are referred help in the assessment of prolapse. Examination should be carried out with dignity and care, using some basic tools that aid in the accurate evaluation of anatomical and functional defects. A standardized assessment system has been used to document findings which should explain everything in understandable terms.
\nThe planning and development of new drugs require high-risk and high-cost investments [1]. This process can involve, for example, studying about 5000–10,000 compounds, a period of 7–12 years, and spending about $800 million for a single drug to be marketed [2]. Thus, alternatives that optimize the process and reduce these costs are considered promising [3].
Nevertheless, there are other issues to the success or failure of drugs that must be considered. The main factors responsible for the lack of success in the production of possible drugs during clinical trials are pharmacokinetic factors, such as absorption, distribution, metabolism, excretion, and toxicities [4].
With the evolution of biotechnology and bioinformatics, promising new approaches for drug planning and optimization have become possible [5]. To reduce costs, risks and have greater efficiency in the production process, the pharmaceutical industry has increasingly used
The
In 1984, the Lock-Key model, proposed by Fisher, explained the theory of ligand-receptor interaction. The model suggested that the interaction between two corresponding structures (ligand and receptor) was due to geometric and energy affinity. In this model, both ligand and receptor were considered rigid structures. The Lock-Key model contributed to the understanding of the mechanism of action of drugs. Nonetheless, it does not explain the interactions in the environment or changes in the spatial conformation of the molecules. Considering these modifications is extremely important, as the conformation of structures can change before and after bonding. Consequently, modern molecular docking tools consider these factors.
Molecular docking assesses the interaction and recognition between macromolecules, in general proteins and ligands [9]. Besides, the algorithm can predict what would happen if these structures interacted in a microenvironment [10]. Prediction of these interactions allows for the creation of structure-based drug design, an advance in drug development as it allows screening of specific molecules for specific targets [11].
Therefore, computer-aided drug design (CADD) uses high-performance computational algorithms to design and optimize molecules to become new drugs. The use of CADD in drug development optimizes the development process, increasing success rate, decreasing laboratory and personnel costs, in addition to producing quick results [3].
Several drugs, currently available for use, have been discovered and improved with the aid of
Molecular docking programs have different approaches and their characterization is according to incremental construction approaches, including shape-based algorithms, genetic algorithms, the Monte Carlo method, and systematic search techniques [17, 18, 19, 20].
Despite the evidence of the effectiveness and advantage of using molecular docking for drug discovery, studies in this area are still incipient for oral diseases [5], which justifies the performance of new studies. Streptococcus mutans (
Additionally, natural products have been a promising source of positive molecules for drug development over the years [25]. Therefore, plants are a promising source of new chemical compounds (phytochemicals) with high biological potential. Phytochemicals are a class of organic compounds synthesized in small amounts from secondary plant metabolism and are related to plant defense, growth, reproduction, and adaptation, among others. Its main classes of compounds are terpenes, alkaloids, and phenolic compounds [26, 27].
In consequence, in this chapter, we performed, by molecular docking, a screening of molecules from plants that showed results of
Ligands were selected from a literature search on phytoconstituents or plants with antimicrobial activity,
Selected compounds for molecular docking in S. mutans target proteins.
The first inclusion criterion was the selection of S. mutans target proteins with high relevance for the virulence of this microorganism [28]. The availability of the crystallographic structures resolved and available in the Protein Data Bank (PDB) was the second inclusion criterion. The protein targets (receptors), their functions, PDB identifiers, and grid box coordinates are presented in Table 1.
Classification | Macromolecule (receiver) | PDB id | Coordinates | Ray (Å) | ||
---|---|---|---|---|---|---|
Function | X | Y | Z | |||
Adhesin | Antigen I/II (V-region) | 1JMM | 34.77 | 20.04 | −7.82 | 20 |
Adhesin | Antigen I/II (carboxy-terminal) | 3QE5 | 74.38 | 44.62 | 141.82 | 25 |
Adhesin | Spap | 3OPU | −20.85 | 53.58 | 6.16 | 15 |
Signaling proteins | Signaling peptide UA159sp | 2I2J | 16.12 | −1.42 | 3.73 | 15 |
Signaling proteins | Signaling peptideTCP3 | 2I2H | 11.9 | −3.45 | 0.99 | 15 |
Signaling proteins | ATP binding protein ComA | 3VX4 | 35.31 | 35.17 | 13.77 | 15 |
Exoenzyme | Glucanosucrase | 3AIC | 192.19 | 44.63 | 197.26 | 15 |
Exoenzyme | Dextranase | 3VMO | 8.71 | −13.02 | −0.67 | 15 |
Exoenzyme | Hemolysin | 2RK5 | 13.57 | 36.99 | 17.83 | 30 |
Names of macromolecules (receivers), identifier in the Protein Data Bank (PDB id), and selected three-dimensional coordinates for docking.
Molecular modeling was performed as described by Rodrigues et al. [29]. Using Hyperchem v. 8.0.3, the chemical structures of all compounds of interest (ligands) were drawn and their geometric structures were optimized using the MM+ force field. Subsequently, a new geometry optimization was performed based on the AM1 semi-empirical method (Austin Model 1). The optimized structures were subjected to conformational analysis using Spartan software for Windows 10.0. The Monte Carlo computational method with 1000 interactions, 100 optimization cycles, and 10 conformations with the lowest energy level was selected. The dihedral angles were evaluated by rotation according to the standard conditions (default) of the program, in which the number of simultaneous variations was 1–8, acyclic chains were subjected to rotations from 60 to 180°, and the torsion rings, to rotations from 30 to 120°. The conformations with the lowest minimum energies were selected and saved in .sdf format. Receivers (protein target) were obtained from the PDB. Receiver, PDB id, and selected three-dimensional coordinates for docking are described in Table 1. Docking simulations were performed in AutoDock 4.2 software. The preparation of receptors and ligands was performed using VEGA ZZ 3.0.1 and MOLEGRO Molecular Viewer 2.5 software. Initially, ligand and receptor structures were saved in .pqbqt format to be used in docking calculations. Then, PyRx 0.9 software was used to assist in the docking steps and the analysis of the results. The “grid maps”, which represent the boxes with three-dimensional coordinates determined for each receiver, were calculated with AutoGrid. Each ligand was docked inside its “grid” with the Lamarckian algorithm implemented in the AutoDock software. The genetics-based algorithm ran 12 simulations per ligand with 2,500,000 energy ratings and a maximum number of 54,000 generations. The crossover rate was increased to 0.8, the gene mutation rate was 0.02, and the number of individuals in each population was 200. All other parameters were left with the default AutoDock settings. The results for each calculation were analyzed to obtain the affinity energy of docking score (Edock) in kcal/mol values for each ligand conformation in its respective complex; structure inaccuracies were ignored in the calculations. To verify the number and positions of hydrogen bonds and non-covalent interactions between each ligand conformation and the catalytic residues of the receptors, the software PyMOL 1.4 and Molegro Molecular Viewer 2.5 were used.
Molecular docking is an
The scores are used as a reference to rank the most stable poses of the ligand. Therefore, the lower the score value, the stronger and more stable the interaction with the selected target. The role and functioning of each of the nine selected S. mutans target proteins are briefly presented below, along with the presentation of the three best ligands for each of the proteins.
The protein-antigen AgI/II is an adhesin present in the cell wall of S. mutans, which recognizes and binds to salivary glycoproteins on the tooth surface, enabling the formation of dental biofilm [31, 32]. Anti-AgI/II antibodies block the adhesion and colonization of S. mutans in the oral cavity [33, 34], justifying the interest in this adhesin in studies aimed at the development of an anticaries therapy [35].
AgI/II adhesin exhibits a functional supramolecular architecture on the cell surface [36], as well as an unusual tertiary structure, where a central variable domain (V-domain) appears like the tip of a formed stem by intertwined and flanked regions rich in alanine and proline [37]. The carboxy-terminal domain (C-domain), connected to a small N-terminal domain that attaches to the cell wall through an anchoring region [38]. AgI/II binding sites for DMBT1 agglutinin are located in the V-domain and C-domain [39].
Docking identified as the best ligands for antigen I/II (V-region) PDB id: 1JMM were the compounds: maldivin-3,5-diglucoside (20) (Edock = −160.78 kJ/mol), licorisoflavan C (17) (Edock = −151.50 kJ/mol), and erystagallin (11) (Edock = −139.85 kJ/mol). Common steric interactions in the complexes formed between Ser818 and Ser697 residues and compounds 17 and 20 were observed. As well as between residue Trp818 and compounds 11 and 17 (Figure 2).
Representations of the interactions between the three best ligands (compounds 20, 17, and 11) and the amino acid residues of the antigen I/II (V-region) PDB id: 1JMM. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
The carboxy-terminal domain of antigen I/II, as well as other proteins in this family, can bind salivary glycoproteins, extracellular matrix molecules, and ligands from other bacteria. This category of proteins is not exclusive to
The I/II antigen is highly conserved and may be associated with M protein in other streptococcal species. The carboxy-terminal region (with 800–1540 amino acid residues) includes proline-rich (P) repeats, conferring hydrophobicity, a transmembrane domain (with 1537–1556 amino acid residues), and an LPXTG motif required for anchorage to the cell wall catalyzed by sortase [32, 41].
The phytochemicals with the most promising linkages with the antigen I/II (carboxy-terminus) PDB id: 3QE5 were: erycristagallin (10) (Edock = −128.98 kJ/mol), sophoraflavanone G (2) (Edock = −105.77 kJ/mol), and erystagallin (11) (Edock = −105.16 kJ/mol). All compounds had in common hydrogen bonds with the Lys1120 residue and steric interactions with the Thr1118 residue, thus indicating that these amino acids are important for minimizing the binding energies and stabilizing the complexes (Figure 3).
Representations of the interactions between the three best ligands (compounds 10, 2, and 11) and the amino acid residues of antigen I/II (carboxy-terminal) PDB id: 3QE5. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
The Spap protein, also called P1, is a multifunctional adhesin that mediates the sucrose-independent adhesion of bacteria to salivary film glycoproteins on the tooth surface. Like other extracellular proteins, this adhesin can produce amyloid, which, in turn, is present in dental biofilms. Thus, this protein directly interferes with the facilitation and adhesion of cariogenic bacteria [21, 42].
The best interactions with Spap PDB id: 3OPU occurred with the compounds: sophoraflavanone G (2) (Edock = −136.98 kJ/mol), erystagallin (11) (Edock = −134.89 kJ/mol), and licorisoflavan (18) (Edock = −129.64 kJ/mol). The common interactions between these ligands and the active site of the protein, which contributed to the low values of the scores of these molecules, are the steric interactions with residues Lys1261 and Pro1210, and hydrogen bonds with residue Asp1208 (Figure 4).
Representations of the interactions between the three best ligands (compounds 2, 11, and 18) and the amino acid residues of Spap PDB id: 3OPU. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
The peptide-mediated quorum sensing in
Quorum-sensing allows bacterial communication, providing benefits during host colonization, defense against competitors, and adaptation to the environment [43, 49]. The chemical details of the signaling molecules of this system in
In a study, conducted by Syvitski et al. [50], peptides in which three or more residues were deleted from the C-terminal region of the signaling peptide UA159sp did not induce genetic competence and inhibited, by competition, the quorum sensing activated by UA159sp. Disruption of the amphipathic α-helix by replacing Phe-7, Phe-11, or Phe-15 residues with a hydrophilic residue resulted in a significant reduction or complete loss of peptide activity. In contrast to peptides truncated at the C-terminal region, these peptides with amino acid substitutions did not compete with UA159sp to activate quorum sensing, suggesting that disruption of the hydrophobic face of the α-helix structure results in a peptide that is not capable of binding to the receptor. Therefore, residues of the C-terminal region of the signaling peptide in the quorum-sensing system of streptococci are extremely important.
Quorum-sensing inhibitor drug design enables the development of more specific treatments for biofilm-dependent infectious diseases [51]. A benefit of using quorum sensing inhibitor drugs is that they are less susceptible to antimicrobial resistance than other antimicrobials, as they exert a lower selective pressure and do not directly kill bacterial cells [52].
Docking with the signaling peptide UA159sp PDB id: 2I2J identified as the best ligands the compounds: erystagallin (11) (Edock = −84.98 kJ/mol), erycristagallin (10) (Edock = −83.99 kJ/mol), and methoxyficifolinol (1) (Edock = −79.76 kJ/mol). In all ligands, the presence of hydrogen bonds with the Ser14 residue and steric interactions with the Ala18 residue is indicative of their importance for the stability of the interaction of these compounds with the active site (Figure 5).
Representations of the interactions between the three best ligands (compounds 11, 10, and 1) and the amino acid residues of the signal peptide UA159sp PDB id: 2I2J. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
TPC3 peptide is a signal peptide synthesized by the mutant strain of
For the signaling peptide TCP3 PDB id: 2I2H the best ligands were: erycristagallin (10) (Edock = −-99.74 kJ/mol), sophoraflavanone G (2) (Edock = −93.23 kJ/mol), and methoxyficifolinol (1) (Edock = −88.16 kJ/mol). As can be seen in Figure 6, hydrogen bonds and steric interactions with Ala18 and Leu10 residues contributed to the energy reduction of these complexes, especially of the best ligands.
Representations of the interactions between the three best ligands (compounds 10, 2, and 1) and the amino acid residues of the signal peptide TCP3 PDB id: 2I2H. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
Quorum sensing is mediated by a signaling molecule autoinducer [53]. This system in some streptococcal species such as
Docking with the ATP binding protein ComA PDB id: 3VX4 identified as the best ligands the compounds: licorisoflavan A (16) (Edock = −-132.56 kJ/mol), licoricidin (15) (Edock = −128.75 kJ/mol), and methoxyficifolinol (1) (Edock = −127.50 kJ/mol). When observing the interactions of the best ligands in the formed complexes, it was observed that hydrogen bonds with residues Thr568 and Ser563 and steric interactions with Lys567 are common, indicating that these interactions contributed to the reduction of the interaction energy and stabilization of the complexes (Figure 7).
Representations of the interactions between the three best ligands (compounds 16, 15, and 1) and the amino acid residues of the ATP binding protein ComA PDB id: 3VX4. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
Glucansucrases or glycosyltransferases (GTFs) are extracellular enzymes, produced by various bacteria, including
The glucanosucrase in
The best ligands that interacted with glucansucrase PDB id: 3AIC in the docking simulation were: erycrystagallin (10) (Edock = −145.72 kJ/mol), malvidin-3,5-diglucoside (20) (Edock = −138.84 kJ/mol), and erystagallin (11) (Edock = −136.44 kJ/mol). Hydrogen bonds with residues Asp480, Asp481, Asn537, and steric interactions with residues Leu433, Glu515, and Trp517 are common to the two best ligands and seem to be important for reducing the energy of formation of these complexes (Figure 8).
Representations of the interactions between the three best ligands (compounds 10, 20, and 11) and the amino acid residues of the glucanoscarase PDB id: 3AIC. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
The docking study conducted out by Kim et al. [63] between rubusoside and
Bhagavathy, Mahendiran, and Kanchana [64], performed molecular docking between seven phytochemical isolates of
Opposing, Islam et al. [65] performed a molecular docking study between epigallocatechin gallate (EGCG) and the same
Some biochemical studies, based on the comparison of amino acid sequences with other glycosyltransferases, revealed that the Asp385 residue is essential for the catalytic reaction [72]. Besides, it was observed that Asp270 from cycloisomalto oligosaccharide glucanotransferases from
Molecular docking performed with the dextranase PDB id: 3VMO identified as the best ligands: licorisoflavan A (16) (Edock = −138.02 kJ/mol), malvidin-3,5-diglucoside (20) (Edock = −136.94 kJ μg/mol), and licoricidin (15) (Edock = −129.73 kJ/mol). Compounds 15 and 16 showed steric interactions in common with residues Tyr257 and Ala559 and showed steric interactions and hydrogen bonds with the key residue Asp385 which has already been identified as essential for catalytic reaction. Diglucoside 20, on the other hand, had a lower energy conformation distinct from compounds 15 and 16 and interacted with other amino acid residues in the active site of the enzyme (Figure 9).
Representations of the interactions between the three best ligands (compounds 16, 20, and 15) and the amino acid residues of dextranase PDB id: 3VMO. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
Hemolysins are exotoxins capable of promoting erythrocyte lysis. They are toxins produced by some species of streptococci [75] and contribute to the virulence process of
Docking with hemolysin PDB id: 3VMO identified as the best ligands the compounds: erycristagallin (10) (Edock = −112.64 kJ/mol), erystagallin (11) (Edock = −104.10 kJ/mol), and methoxyficifolinol (1) (Edock = −100.63 kJ/mol). The steric interactions and hydrogen bonds with Asn21, Asn24, and Asp30 residues were common for compounds 10 and 11, and seem to be important for the stabilization of the complexes. Compound 1, despite belonging to the same chemical class as compounds 10 and 11, showed a more stable conformation in another position of the active site, consequently, is stabilized by interactions with different amino acid residues, but which contributed less to the stabilization of the complex (Figure 10).
Representations of the interactions between the three best ligands (compounds 10, 11, and 1) and the amino acid residues of hemolysin PDB id: 2RK5. Blue dashed lines represent hydrogen bonds and red dashed lines represent steric interactions.
In the research phase for phytochemicals with activity against
Five phytocompounds evaluated were elected as one of the three best ligands for at least three target proteins, highlighting the following compounds: 11 (erystagallin) (highlighted for 6 targets), 10 (erycristagallin) (highlighted for 5 targets), 1 (methoxyficifonilol) (highlighted for 4 targets), 20 (malvidin-3,5-diglucoside), and 2 (sophoraflavanone G), which provided indications of a possible and desirable multi-target action of these compounds.
Based on these findings, these selected compounds should have theirs
This work was supported by National Council for Scientific and Technological Development (CNPq) [grant number 308590/2017-1], and Coordination for the Improvement of Higher Education Personnel (CAPES), Brazil [financing code 001].
The authors declare that they have no conflict of interest with this manuscript.
Edited by Jan Oxholm Gordeladze, ISBN 978-953-51-3020-8, Print ISBN 978-953-51-3019-2, 336 pages,
\nPublisher: IntechOpen
\nChapters published March 22, 2017 under CC BY 3.0 license
\nDOI: 10.5772/61430
\nEdited Volume
This book serves as a comprehensive survey of the impact of vitamin K2 on cellular functions and organ systems, indicating that vitamin K2 plays an important role in the differentiation/preservation of various cell phenotypes and as a stimulator and/or mediator of interorgan cross talk. Vitamin K2 binds to the transcription factor SXR/PXR, thus acting like a hormone (very much in the same manner as vitamin A and vitamin D). Therefore, vitamin K2 affects a multitude of organ systems, and it is reckoned to be one positive factor in bringing about "longevity" to the human body, e.g., supporting the functions/health of different organ systems, as well as correcting the functioning or even "curing" ailments striking several organs in our body.
\\n\\nChapter 1 Introductory Chapter: Vitamin K2 by Jan Oxholm Gordeladze
\\n\\nChapter 2 Vitamin K, SXR, and GGCX by Kotaro Azuma and Satoshi Inoue
\\n\\nChapter 3 Vitamin K2 Rich Food Products by Muhammad Yasin, Masood Sadiq Butt and Aurang Zeb
\\n\\nChapter 4 Menaquinones, Bacteria, and Foods: Vitamin K2 in the Diet by Barbara Walther and Magali Chollet
\\n\\nChapter 5 The Impact of Vitamin K2 on Energy Metabolism by Mona Møller, Serena Tonstad, Tone Bathen and Jan Oxholm Gordeladze
\\n\\nChapter 6 Vitamin K2 and Bone Health by Niels Erik Frandsen and Jan Oxholm Gordeladze
\\n\\nChapter 7 Vitamin K2 and its Impact on Tooth Epigenetics by Jan Oxholm Gordeladze, Maria A. Landin, Gaute Floer Johnsen, Håvard Jostein Haugen and Harald Osmundsen
\\n\\nChapter 8 Anti-Inflammatory Actions of Vitamin K by Stephen J. Hodges, Andrew A. Pitsillides, Lars M. Ytrebø and Robin Soper
\\n\\nChapter 9 Vitamin K2: Implications for Cardiovascular Health in the Context of Plant-Based Diets, with Applications for Prostate Health by Michael S. Donaldson
\\n\\nChapter 11 Vitamin K2 Facilitating Inter-Organ Cross-Talk by Jan O. Gordeladze, Håvard J. Haugen, Gaute Floer Johnsen and Mona Møller
\\n\\nChapter 13 Medicinal Chemistry of Vitamin K Derivatives and Metabolites by Shinya Fujii and Hiroyuki Kagechika
\\n"}]'},components:[{type:"htmlEditorComponent",content:'This book serves as a comprehensive survey of the impact of vitamin K2 on cellular functions and organ systems, indicating that vitamin K2 plays an important role in the differentiation/preservation of various cell phenotypes and as a stimulator and/or mediator of interorgan cross talk. Vitamin K2 binds to the transcription factor SXR/PXR, thus acting like a hormone (very much in the same manner as vitamin A and vitamin D). Therefore, vitamin K2 affects a multitude of organ systems, and it is reckoned to be one positive factor in bringing about "longevity" to the human body, e.g., supporting the functions/health of different organ systems, as well as correcting the functioning or even "curing" ailments striking several organs in our body.
\n\nChapter 1 Introductory Chapter: Vitamin K2 by Jan Oxholm Gordeladze
\n\nChapter 2 Vitamin K, SXR, and GGCX by Kotaro Azuma and Satoshi Inoue
\n\nChapter 3 Vitamin K2 Rich Food Products by Muhammad Yasin, Masood Sadiq Butt and Aurang Zeb
\n\nChapter 4 Menaquinones, Bacteria, and Foods: Vitamin K2 in the Diet by Barbara Walther and Magali Chollet
\n\nChapter 5 The Impact of Vitamin K2 on Energy Metabolism by Mona Møller, Serena Tonstad, Tone Bathen and Jan Oxholm Gordeladze
\n\nChapter 6 Vitamin K2 and Bone Health by Niels Erik Frandsen and Jan Oxholm Gordeladze
\n\nChapter 7 Vitamin K2 and its Impact on Tooth Epigenetics by Jan Oxholm Gordeladze, Maria A. Landin, Gaute Floer Johnsen, Håvard Jostein Haugen and Harald Osmundsen
\n\nChapter 8 Anti-Inflammatory Actions of Vitamin K by Stephen J. Hodges, Andrew A. Pitsillides, Lars M. Ytrebø and Robin Soper
\n\nChapter 9 Vitamin K2: Implications for Cardiovascular Health in the Context of Plant-Based Diets, with Applications for Prostate Health by Michael S. Donaldson
\n\nChapter 11 Vitamin K2 Facilitating Inter-Organ Cross-Talk by Jan O. Gordeladze, Håvard J. Haugen, Gaute Floer Johnsen and Mona Møller
\n\nChapter 13 Medicinal Chemistry of Vitamin K Derivatives and Metabolites by Shinya Fujii and Hiroyuki Kagechika
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His studies in robotics lead him not only to a PhD degree but also inspired him to co-found and build the International Journal of Advanced Robotic Systems - world's first Open Access journal in the field of robotics.",institutionString:null,institution:{name:"TU Wien",country:{name:"Austria"}}},{id:"441",title:"Ph.D.",name:"Jaekyu",middleName:null,surname:"Park",slug:"jaekyu-park",fullName:"Jaekyu Park",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/441/images/1881_n.jpg",biography:null,institutionString:null,institution:{name:"LG Corporation (South Korea)",country:{name:"Korea, South"}}},{id:"465",title:"Dr.",name:"Christian",middleName:null,surname:"Martens",slug:"christian-martens",fullName:"Christian Martens",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Rheinmetall (Germany)",country:{name:"Germany"}}},{id:"479",title:"Dr.",name:"Valentina",middleName:null,surname:"Colla",slug:"valentina-colla",fullName:"Valentina Colla",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/479/images/358_n.jpg",biography:null,institutionString:null,institution:{name:"Sant'Anna School of Advanced Studies",country:{name:"Italy"}}},{id:"494",title:"PhD",name:"Loris",middleName:null,surname:"Nanni",slug:"loris-nanni",fullName:"Loris Nanni",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/494/images/system/494.jpg",biography:"Loris Nanni received his Master Degree cum laude on June-2002 from the University of Bologna, and the April 26th 2006 he received his Ph.D. in Computer Engineering at DEIS, University of Bologna. On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. His research interests include pattern recognition, bioinformatics, and biometric systems (fingerprint classification and recognition, signature verification, face recognition).",institutionString:null,institution:null},{id:"496",title:"Dr.",name:"Carlos",middleName:null,surname:"Leon",slug:"carlos-leon",fullName:"Carlos Leon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Seville",country:{name:"Spain"}}},{id:"512",title:"Dr.",name:"Dayang",middleName:null,surname:"Jawawi",slug:"dayang-jawawi",fullName:"Dayang Jawawi",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Technology Malaysia",country:{name:"Malaysia"}}},{id:"528",title:"Dr.",name:"Kresimir",middleName:null,surname:"Delac",slug:"kresimir-delac",fullName:"Kresimir Delac",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/528/images/system/528.jpg",biography:"K. Delac received his B.Sc.E.E. degree in 2003 and is currentlypursuing a Ph.D. degree at the University of Zagreb, Faculty of Electrical Engineering andComputing. His current research interests are digital image analysis, pattern recognition andbiometrics.",institutionString:null,institution:{name:"University of Zagreb",country:{name:"Croatia"}}},{id:"557",title:"Dr.",name:"Andon",middleName:"Venelinov",surname:"Topalov",slug:"andon-topalov",fullName:"Andon Topalov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/557/images/1927_n.jpg",biography:"Dr. Andon V. Topalov received the MSc degree in Control Engineering from the Faculty of Information Systems, Technologies, and Automation at Moscow State University of Civil Engineering (MGGU) in 1979. He then received his PhD degree in Control Engineering from the Department of Automation and Remote Control at Moscow State Mining University (MGSU), Moscow, in 1984. From 1985 to 1986, he was a Research Fellow in the Research Institute for Electronic Equipment, ZZU AD, Plovdiv, Bulgaria. In 1986, he joined the Department of Control Systems, Technical University of Sofia at the Plovdiv campus, where he is presently a Full Professor. He has held long-term visiting Professor/Scholar positions at various institutions in South Korea, Turkey, Mexico, Greece, Belgium, UK, and Germany. And he has coauthored one book and authored or coauthored more than 80 research papers in conference proceedings and journals. His current research interests are in the fields of intelligent control and robotics.",institutionString:null,institution:{name:"Technical University of Sofia",country:{name:"Bulgaria"}}},{id:"585",title:"Prof.",name:"Munir",middleName:null,surname:"Merdan",slug:"munir-merdan",fullName:"Munir Merdan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/585/images/system/585.jpg",biography:"Munir Merdan received the M.Sc. degree in mechanical engineering from the Technical University of Sarajevo, Bosnia and Herzegovina, in 2001, and the Ph.D. degree in electrical engineering from the Vienna University of Technology, Vienna, Austria, in 2009.Since 2005, he has been at the Automation and Control Institute, Vienna University of Technology, where he is currently a Senior Researcher. His research interests include the application of agent technology for achieving agile control in the manufacturing environment.",institutionString:null,institution:null},{id:"605",title:"Prof",name:"Dil",middleName:null,surname:"Hussain",slug:"dil-hussain",fullName:"Dil Hussain",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/605/images/system/605.jpg",biography:"Dr. Dil Muhammad Akbar Hussain is a professor of Electronics Engineering & Computer Science at the Department of Energy Technology, Aalborg University Denmark. Professor Akbar has a Master degree in Digital Electronics from Govt. College University, Lahore Pakistan and a P-hD degree in Control Engineering from the School of Engineering and Applied Sciences, University of Sussex United Kingdom. Aalborg University has Two Satellite Campuses, one in Copenhagen (Aalborg University Copenhagen) and the other in Esbjerg (Aalborg University Esbjerg).\n· He is a member of prestigious IEEE (Institute of Electrical and Electronics Engineers), and IAENG (International Association of Engineers) organizations. \n· He is the chief Editor of the Journal of Software Engineering.\n· He is the member of the Editorial Board of International Journal of Computer Science and Software Technology (IJCSST) and International Journal of Computer Engineering and Information Technology. \n· He is also the Editor of Communication in Computer and Information Science CCIS-20 by Springer.\n· Reviewer For Many Conferences\nHe is the lead person in making collaboration agreements between Aalborg University and many universities of Pakistan, for which the MOU’s (Memorandum of Understanding) have been signed.\nProfessor Akbar is working in Academia since 1990, he started his career as a Lab demonstrator/TA at the University of Sussex. After finishing his P. hD degree in 1992, he served in the Industry as a Scientific Officer and continued his academic career as a visiting scholar for a number of educational institutions. In 1996 he joined National University of Science & Technology Pakistan (NUST) as an Associate Professor; NUST is one of the top few universities in Pakistan. In 1999 he joined an International Company Lineo Inc, Canada as Manager Compiler Group, where he headed the group for developing Compiler Tool Chain and Porting of Operating Systems for the BLACKfin processor. The processor development was a joint venture by Intel and Analog Devices. In 2002 Lineo Inc., was taken over by another company, so he joined Aalborg University Denmark as an Assistant Professor.\nProfessor Akbar has truly a multi-disciplined career and he continued his legacy and making progress in many areas of his interests both in teaching and research. 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Everyone must undergo this phase of life at his or her own time and pace. In the broader sense, ageing reflects all the changes taking place over the course of life. These changes start from birth—one grows, develops and attains maturity. To the young, ageing is exciting. Middle age is the time when people notice the age-related changes like greying of hair, wrinkled skin and a fair amount of physical decline. Even the healthiest, aesthetically fit cannot escape these changes. Slow and steady physical impairment and functional disability are noticed resulting in increased dependency in the period of old age. According to World Health Organization, ageing is a course of biological reality which starts at conception and ends with death. It has its own dynamics, much beyond human control. However, this process of ageing is also subject to the constructions by which each society makes sense of old age. In most of the developed countries, the age of 60 is considered equivalent to retirement age and it is said to be the beginning of old age. In this chapter, you understand the details of ageing processes and associated physiological changes.",book:{id:"6381",slug:"gerontology",title:"Gerontology",fullTitle:"Gerontology"},signatures:"Shilpa Amarya, Kalyani Singh and Manisha Sabharwal",authors:[{id:"226573",title:"Ph.D.",name:"Shilpa",middleName:null,surname:"Amarya",slug:"shilpa-amarya",fullName:"Shilpa Amarya"},{id:"226593",title:"Dr.",name:"Kalyani",middleName:null,surname:"Singh",slug:"kalyani-singh",fullName:"Kalyani Singh"},{id:"243264",title:"Dr.",name:"Manisha",middleName:null,surname:"Sabharwal",slug:"manisha-sabharwal",fullName:"Manisha Sabharwal"}]},{id:"27237",title:"Emotional Intelligence",slug:"emotional-intelligence",totalDownloads:5774,totalCrossrefCites:6,totalDimensionsCites:9,abstract:null,book:{id:"679",slug:"emotional-intelligence-new-perspectives-and-applications",title:"Emotional Intelligence",fullTitle:"Emotional Intelligence - New Perspectives and Applications"},signatures:"Adrian Furnham",authors:[{id:"85492",title:"Prof.",name:"Adrian",middleName:null,surname:"Furnham",slug:"adrian-furnham",fullName:"Adrian Furnham"}]},{id:"70731",title:"Theoretical Perspective of Traditional Counseling",slug:"theoretical-perspective-of-traditional-counseling",totalDownloads:1605,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"This chapter discusses the theoretical perspective of traditional counseling from an African context. Traditional counseling involves a broad perspective that enhances learning for transformation and integration of sociocultural values that are peculiar to each human society. A cursory review of the literature suggests that the concept of traditional counseling is rooted in traditional systems of knowledge and sociocultural customs and practices, and it promotes a collective approach to problem identification, resolution, and management. The traditional counseling process centers on four aspects: traditional counselor, client, family, and community. The key elements that inform the theoretical framework of traditional counseling from an African perspective are: cultural context, collective belief system, and initiation rituals Traditional systems of knowledge deemed essential for each generation are passed on successively to the next generation by elderly people who do not only have the necessary wisdom and experience, but are also adorned with social competences and skills.",book:{id:"9136",slug:"counseling-and-therapy",title:"Counseling and Therapy",fullTitle:"Counseling and Therapy"},signatures:"Hector Chiboola",authors:[{id:"314172",title:"Prof.",name:"Hector",middleName:null,surname:"Chiboola",slug:"hector-chiboola",fullName:"Hector Chiboola"}]},{id:"55388",title:"Beauty, Body Image, and the Media",slug:"beauty-body-image-and-the-media",totalDownloads:7764,totalCrossrefCites:5,totalDimensionsCites:12,abstract:"This chapter analyses the role of the mass media in people’s perceptions of beauty. We summarize the research literature on the mass media, both traditional media and online social media, and how they appear to interact with psychological factors to impact appearance concerns and body image disturbances. There is a strong support for the idea that traditional forms of media (e.g. magazines and music videos) affect perceptions of beauty and appearance concerns by leading women to internalize a very slender body type as ideal or beautiful. Rather than simply being passive recipients of unrealistic beauty ideals communicated to them via the media, a great number of individuals actually seek out idealized images in the media. Finally, we review what is known about the role of social media in impacting society’s perception of beauty and notions of idealized physical forms. Social media are more interactive than traditional media and the effects of self‐presentation strategies on perceptions of beauty have just begun to be studied. This is an emerging area of research that is of high relevance to researchers and clinicians interested in body image and appearance concerns.",book:{id:"5925",slug:"perception-of-beauty",title:"Perception of Beauty",fullTitle:"Perception of Beauty"},signatures:"Jennifer S. Mills, Amy Shannon and Jacqueline Hogue",authors:[{id:"202110",title:"Dr.",name:"Jennifer S.",middleName:null,surname:"Mills",slug:"jennifer-s.-mills",fullName:"Jennifer S. Mills"}]}],onlineFirstChaptersFilter:{topicId:"21",limit:6,offset:0},onlineFirstChaptersCollection:[{id:"83107",title:"Helping BIPOC LGBTQIA+ Families Through Inclusive Therapy and Advocacy",slug:"helping-bipoc-lgbtqia-families-through-inclusive-therapy-and-advocacy",totalDownloads:0,totalDimensionsCites:null,doi:"10.5772/intechopen.106695",abstract:null,book:{id:"11781",title:"Family Therapy - Recent Advances in Clinical and Crisis Settings",coverURL:"https://cdn.intechopen.com/books/images_new/11781.jpg"},signatures:"Lucy Parker-Barnes, Noel McKillip and Carolyn Powell"},{id:"83099",title:"Values-Flow in Contextual Psychotherapy: The ‘What’, ‘Why’, and ‘How’ of Sustainable Values-Based Behaviour",slug:"values-flow-in-contextual-psychotherapy-the-what-why-and-how-of-sustainable-values-based-behaviour",totalDownloads:2,totalDimensionsCites:null,doi:"10.5772/intechopen.106594",abstract:"Flow - enjoyed and fully absorbed engagement in meaningful and contextually bounded activities - is widely underutilised in psychotherapy and mental health settings. Two gold standard therapies, Acceptance and Commitment Therapy (ACT) and Dialectical Behaviour Therapy (DBT), while powerful and effective in many ways, would benefit from systematic models that move from initiating positive change to sustaining meaningful change. This chapter introduces ‘Values-Flow’ – an approach aimed at building commitment and sustainable engagement in psychotherapy and values-based behaviour in working adults struggling with sub-optimal functioning. We first introduce Values-Flow and describe how it may benefit psychotherapy skills practice in everyday life. Next, we discuss why Values-Flow is relevant and enhances the practice of ACT and DBT strategies, helping to sustain engagement and creative practice of values-based actions outside of sessions. We then describe the ‘Values-Flow’ framework, which incorporates VIVA (Virtue, Involve, Vital, Accepting) and ARIA (Attend, Reflect, Inform, Act) tools that develop commitment for values-based practice in daily life. We conclude with a case-example of how Values-Flow can build commitment and sustainable engagement in homework completion in psychotherapy.",book:{id:"11444",title:"Happiness - Biopsychosocial and Anthropological Perspectives",coverURL:"https://cdn.intechopen.com/books/images_new/11444.jpg"},signatures:"Cedomir Ignjatovic, Margaret L. Kern and Lindsay G. Oades"},{id:"83100",title:"Factors Affecting the Happiness of Korean University Students",slug:"factors-affecting-the-happiness-of-korean-university-students",totalDownloads:2,totalDimensionsCites:null,doi:"10.5772/intechopen.106296",abstract:"As of 2020, in Korea, as 72.5% of high-school graduates go on to college and college period has an impact on the social development of Korean youth, it is very important to increase the sense of happiness of college students. However, there are new terminologies to express the situation in which how young people in Korea feel the difficulties in their lives, such as “Hell Chosun, 88-Dollar-Generation, N-Give-up-Generation, and Spoon-Social-Rank.” This chapter summarizes the factors related to the happiness of college students in South Korea, such as depression, interpersonal relationships, and self-efficacy, to suggest educational programs to promote the happiness of young people in Korea.",book:{id:"11444",title:"Happiness - Biopsychosocial and Anthropological Perspectives",coverURL:"https://cdn.intechopen.com/books/images_new/11444.jpg"},signatures:"Soo-Koung Jun"},{id:"83027",title:"Coping Strategies and Meta-Worry in Adolescents’ Adjustment during COVID-19 Pandemic",slug:"coping-strategies-and-meta-worry-in-adolescents-adjustment-during-covid-19-pandemic",totalDownloads:1,totalDimensionsCites:0,doi:"10.5772/intechopen.106258",abstract:"With the beginning of the COVID-19 pandemic, several limitations and stressful changes have been introduced in adolescent’s daily life. Particularly, Italian teenagers were the first among western populations to experience fears of infection, home confinement, and social restrictions due to a long lockdown period (10 weeks). This study explores the role of coping strategies (task-oriented, emotion-oriented, and avoidance coping) and meta-beliefs about worry as vulnerability factors associated with adolescents’ anxiety. A community sample of adolescents (N = 284, aged 16–18 y.o.) answered questionnaires assessing anxiety symptoms (RCMAS-2), meta-cognitive beliefs and processes about worry (MCQ-C), and coping strategies (CISS). Results show that 37% of participants report clinically elevated anxiety. Emotion-centered coping predicted higher anxiety, whereas task-centered coping resulted associated with decreased anxiety. Cognitive monitoring about their own worry contributes, but to a lesser extent, to higher levels of anxiety. The implications for the intervention are discussed, especially the need to enhance the coping skills of adolescents and mitigate the stress of the COVID-19 pandemic, which could last for a long time.",book:{id:"10671",title:"Adolescences",coverURL:"https://cdn.intechopen.com/books/images_new/10671.jpg"},signatures:"Loredana Benedetto, Ilenia Schipilliti and Massimo Ingrassia"},{id:"83023",title:"Gestational Tryptophan Fluctuation Underlying Ontogenetic Origin of Neuropsychiatric Disorders",slug:"gestational-tryptophan-fluctuation-underlying-ontogenetic-origin-of-neuropsychiatric-disorders",totalDownloads:5,totalDimensionsCites:0,doi:"10.5772/intechopen.106421",abstract:"Neuropsychiatry underlies personality development and social functioning. Borderline personality disorder exhibits high trait aggression and is associated with tryptophan hydroxylase polymorphisms. The acute tryptophan depletion reduces plasma and cerebrospinal fluid tryptophan availability and brain serotonin concentrations, leading to alterations in personality and trait-related behaviors. Tryptophan is essential for fatal neurodevelopment and immunomodulation in pregnancy. Gestational tryptophan fluctuation induced by maternal metabolic disorders or drug administrations may account for the maternal-fetal transmission determining neurogenesis and microbial development, consequentially shaping the long-standing patterns of thinking and behavior. However, it is not possible to assess the gestational tryptophan exposure effects on fetal brain and gastrointestinal system in humans for ethical reasons. The maternal–fetal microbe transmission in rodents during gestation, vaginal delivery, and breastfeeding is inevitable. Chicken embryo may be an alternative and evidence from the chicken embryo model reveals that gestational tryptophan fluctuation, i.e., exposed to excessive tryptophan or its metabolite, serotonin, attenuates aggressiveness and affects peer sociometric status. This chapter discusses the gestational tryptophan fluctuation as a risk factor of personality disorders in offspring and the prevention of personality disorders by dietary tryptophan control and medication therapy management during pregnancy.",book:{id:"11782",title:"Personality Traits - The Role in Psychopathology",coverURL:"https://cdn.intechopen.com/books/images_new/11782.jpg"},signatures:"Xiaohong Huang, Xiaohua Li and Heng-Wei Cheng"},{id:"82982",title:"The Well-Being in the Children and Adolescents with ADHD: Possible Influencing Factors and How to Improve It",slug:"the-well-being-in-the-children-and-adolescents-with-adhd-possible-influencing-factors-and-how-to-imp",totalDownloads:2,totalDimensionsCites:0,doi:"10.5772/intechopen.106596",abstract:"In recent years, academics have increasingly emphasized the importance of research into the well-being of children and adolescents. This is because well-being plays an important role in the development of children and adolescents. The literature reports that high levels of well-being facilitate positive functioning in children and adolescents. They contribute to the overall development of the individual and are a key factor in helping children and adolescents to integrate into society. ADHD, the most prevalent neurodevelopmental disorder, affects more than 5% of children and adolescents, and the distress caused by its symptom can seriously undermine the well-being of children and adolescents. Therefore, this chapter discusses this noticeable issue focusing on the following key parts: An understanding of the well-being in children and adolescents, the factors that affect the well-being of children and adolescents with ADHD, and how to improve the well-being of children and adolescents with ADHD.",book:{id:"11444",title:"Happiness - Biopsychosocial and Anthropological Perspectives",coverURL:"https://cdn.intechopen.com/books/images_new/11444.jpg"},signatures:"Jenson Yin and Jie Luo"}],onlineFirstChaptersTotal:67},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:0,limit:8,total:null},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:90,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:108,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:33,numberOfPublishedChapters:330,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:14,numberOfPublishedChapters:145,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:9,numberOfPublishedChapters:141,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:124,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:112,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:22,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:11,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:"2753-6580",doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"10",title:"Physiology",doi:"10.5772/intechopen.72796",issn:"2631-8261",scope:"Modern physiology requires a comprehensive understanding of the integration of tissues and organs throughout the mammalian body, including the cooperation between structure and function at the cellular and molecular levels governed by gene and protein expression. While a daunting task, learning is facilitated by identifying common and effective signaling pathways mediated by a variety of factors employed by nature to preserve and sustain homeostatic life. \r\nAs a leading example, the cellular interaction between intracellular concentration of Ca+2 increases, and changes in plasma membrane potential is integral for coordinating blood flow, governing the exocytosis of neurotransmitters, and modulating gene expression and cell effector secretory functions. Furthermore, in this manner, understanding the systemic interaction between the cardiovascular and nervous systems has become more important than ever as human populations' life prolongation, aging and mechanisms of cellular oxidative signaling are utilised for sustaining life. \r\nAltogether, physiological research enables our identification of distinct and precise points of transition from health to the development of multimorbidity throughout the inevitable aging disorders (e.g., diabetes, hypertension, chronic kidney disease, heart failure, peptic ulcer, inflammatory bowel disease, age-related macular degeneration, cancer). With consideration of all organ systems (e.g., brain, heart, lung, gut, skeletal and smooth muscle, liver, pancreas, kidney, eye) and the interactions thereof, this Physiology Series will address the goals of resolving (1) Aging physiology and chronic disease progression (2) Examination of key cellular pathways as they relate to calcium, oxidative stress, and electrical signaling, and (3) how changes in plasma membrane produced by lipid peroxidation products can affect aging physiology, covering new research in the area of cell, human, plant and animal physiology.",coverUrl:"https://cdn.intechopen.com/series/covers/10.jpg",latestPublicationDate:"July 20th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:14,editor:{id:"35854",title:"Prof.",name:"Tomasz",middleName:null,surname:"Brzozowski",slug:"tomasz-brzozowski",fullName:"Tomasz Brzozowski",profilePictureURL:"https://mts.intechopen.com/storage/users/35854/images/system/35854.jpg",biography:"Prof. Dr. Thomas Brzozowski works as a professor of Human Physiology and is currently Chairman at the Department of Physiology and is V-Dean of the Medical Faculty at Jagiellonian University Medical College, Cracow, Poland. His primary area of interest is physiology and pathophysiology of the gastrointestinal (GI) tract, with the major focus on the mechanism of GI mucosal defense, protection, and ulcer healing. He was a postdoctoral NIH fellow at the University of California and the Gastroenterology VA Medical Center, Irvine, Long Beach, CA, USA, and at the Gastroenterology Clinics Erlangen-Nuremberg and Munster in Germany. He has published 290 original articles in some of the most prestigious scientific journals and seven book chapters on the pathophysiology of the GI tract, gastroprotection, ulcer healing, drug therapy of peptic ulcers, hormonal regulation of the gut, and inflammatory bowel disease.",institutionString:null,institution:{name:"Jagiellonian University",institutionURL:null,country:{name:"Poland"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"10",title:"Animal Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/10.jpg",isOpenForSubmission:!0,annualVolume:11406,editor:{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. Dr. Rutland has also written popular science books for the public. https://orcid.org/0000-0002-2009-4898. www.nottingham.ac.uk/vet/people/catrin.rutland",institutionString:null,institution:{name:"University of Nottingham",institutionURL:null,country:{name:"United Kingdom"}}},editorTwo:null,editorThree:null},{id:"11",title:"Cell Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/11.jpg",isOpenForSubmission:!0,annualVolume:11407,editor:{id:"133493",title:"Prof.",name:"Angel",middleName:null,surname:"Catala",slug:"angel-catala",fullName:"Angel Catala",profilePictureURL:"https://mts.intechopen.com/storage/users/133493/images/3091_n.jpg",biography:"Prof. Dr. Angel Catalá \r\nShort Biography Angel Catalá was born in Rodeo (San Juan, Argentina). He studied \r\nchemistry at the Universidad Nacional de La Plata, Argentina, where received aPh.D. degree in chemistry (Biological Branch) in 1965. From\r\n1964 to 1974, he worked as Assistant in Biochemistry at the School of MedicineUniversidad Nacional de La Plata, Argentina. From 1974 to 1976, he was a Fellowof the National Institutes of Health (NIH) at the University of Connecticut, Health Center, USA. From 1985 to 2004, he served as a Full Professor oBiochemistry at the Universidad Nacional de La Plata, Argentina. He is Member ofthe National Research Council (CONICET), Argentina, and Argentine Society foBiochemistry and Molecular Biology (SAIB). His laboratory has been interested for manyears in the lipid peroxidation of biological membranes from various tissues and different species. Professor Catalá has directed twelve doctoral theses, publishedover 100 papers in peer reviewed journals, several chapters in books andtwelve edited books. Angel Catalá received awards at the 40th InternationaConference Biochemistry of Lipids 1999: Dijon (France). W inner of the Bimbo PanAmerican Nutrition, Food Science and Technology Award 2006 and 2012, South AmericaHuman Nutrition, Professional Category. 2006 award in pharmacology, Bernardo\r\nHoussay, in recognition of his meritorious works of research. Angel Catalá belongto the Editorial Board of Journal of lipids, International Review of Biophysical ChemistryFrontiers in Membrane Physiology and Biophysics, World Journal oExperimental Medicine and Biochemistry Research International, W orld Journal oBiological Chemistry, Oxidative Medicine and Cellular Longevity, Diabetes and thePancreas, International Journal of Chronic Diseases & Therapy, International Journal oNutrition, Co-Editor of The Open Biology Journal.",institutionString:null,institution:{name:"National University of La Plata",institutionURL:null,country:{name:"Argentina"}}},editorTwo:null,editorThree:null},{id:"12",title:"Human Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/12.jpg",isOpenForSubmission:!0,annualVolume:11408,editor:{id:"195829",title:"Prof.",name:"Kunihiro",middleName:null,surname:"Sakuma",slug:"kunihiro-sakuma",fullName:"Kunihiro Sakuma",profilePictureURL:"https://mts.intechopen.com/storage/users/195829/images/system/195829.jpg",biography:"Professor Kunihiro Sakuma, Ph.D., currently works in the Institute for Liberal Arts at the Tokyo Institute of Technology. He is a physiologist working in the field of skeletal muscle. He was awarded his sports science diploma in 1995 by the University of Tsukuba and began his scientific work at the Department of Physiology, Aichi Human Service Center, focusing on the molecular mechanism of congenital muscular dystrophy and normal muscle regeneration. His interest later turned to the molecular mechanism and attenuating strategy of sarcopenia (age-related muscle atrophy). His opinion is to attenuate sarcopenia by improving autophagic defects using nutrient- and pharmaceutical-based treatments.",institutionString:null,institution:{name:"Tokyo Institute of Technology",institutionURL:null,country:{name:"Japan"}}},editorTwo:{id:"331519",title:"Dr.",name:"Kotomi",middleName:null,surname:"Sakai",slug:"kotomi-sakai",fullName:"Kotomi Sakai",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000031QtFXQA0/Profile_Picture_1637053227318",biography:"Senior researcher Kotomi Sakai, Ph.D., MPH, works at the Research Organization of Science and Technology in Ritsumeikan University. She is a researcher in the geriatric rehabilitation and public health field. She received Ph.D. from Nihon University and MPH from St.Luke’s International University. Her main research interest is sarcopenia in older adults, especially its association with nutritional status. Additionally, to understand how to maintain and improve physical function in older adults, to conduct studies about the mechanism of sarcopenia and determine when possible interventions are needed.",institutionString:null,institution:{name:"Ritsumeikan University",institutionURL:null,country:{name:"Japan"}}},editorThree:null},{id:"13",title:"Plant Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/13.jpg",isOpenForSubmission:!0,annualVolume:11409,editor:{id:"332229",title:"Prof.",name:"Jen-Tsung",middleName:null,surname:"Chen",slug:"jen-tsung-chen",fullName:"Jen-Tsung Chen",profilePictureURL:"https://mts.intechopen.com/storage/users/332229/images/system/332229.png",biography:"Dr. Jen-Tsung Chen is currently a professor at the National University of Kaohsiung, Taiwan. He teaches cell biology, genomics, proteomics, medicinal plant biotechnology, and plant tissue culture. 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