Representing the types and structure of phytocompounds present in the green tea with their therapeutic benefits.
\\n\\n
IntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\\n\\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\\n\\nLaunching 2021
\\n\\nArtificial Intelligence, ISSN 2633-1403
\\n\\nVeterinary Medicine and Science, ISSN 2632-0517
\\n\\nBiochemistry, ISSN 2632-0983
\\n\\nBiomedical Engineering, ISSN 2631-5343
\\n\\nInfectious Diseases, ISSN 2631-6188
\\n\\nPhysiology (Coming Soon)
\\n\\nDentistry (Coming Soon)
\\n\\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\\n\\nNote: Edited in October 2021
\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/132"}},components:[{type:"htmlEditorComponent",content:'With the desire to make book publishing more relevant for the digital age and offer innovative Open Access publishing options, we are thrilled to announce the launch of our new publishing format: IntechOpen Book Series.
\n\nDesigned to cover fast-moving research fields in rapidly expanding areas, our Book Series feature a Topic structure allowing us to present the most relevant sub-disciplines. Book Series are headed by Series Editors, and a team of Topic Editors supported by international Editorial Board members. Topics are always open for submissions, with an Annual Volume published each calendar year.
\n\nAfter a robust peer-review process, accepted works are published quickly, thanks to Online First, ensuring research is made available to the scientific community without delay.
\n\nOur innovative Book Series format brings you:
\n\nIntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\n\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\n\nLaunching 2021
\n\nArtificial Intelligence, ISSN 2633-1403
\n\nVeterinary Medicine and Science, ISSN 2632-0517
\n\nBiochemistry, ISSN 2632-0983
\n\nBiomedical Engineering, ISSN 2631-5343
\n\nInfectious Diseases, ISSN 2631-6188
\n\nPhysiology (Coming Soon)
\n\nDentistry (Coming Soon)
\n\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\n\nNote: Edited in October 2021
\n'}],latestNews:[{slug:"intechopen-supports-asapbio-s-new-initiative-publish-your-reviews-20220729",title:"IntechOpen Supports ASAPbio’s New Initiative Publish Your Reviews"},{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"}]},book:{item:{type:"book",id:"10384",leadTitle:null,fullTitle:"Practical Applications in Reliability Engineering",title:"Practical Applications in Reliability Engineering",subtitle:null,reviewType:"peer-reviewed",abstract:"This book compiles and examines advanced technologies in the field of reliability and risk analysis. It presents comprehensive methodologies and up-to-date software along with examples of practical case studies from industrial areas to provide a realistic and authentic platform for readers.",isbn:"978-1-83968-400-5",printIsbn:"978-1-83968-399-2",pdfIsbn:"978-1-83968-401-2",doi:"10.5772/intechopen.91570",price:100,priceEur:109,priceUsd:129,slug:"practical-applications-in-reliability-engineering",numberOfPages:94,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"377d3c041a06cfcfc99bd906fdbbbf46",bookSignature:"Muhammad Zubair",publishedDate:"June 16th 2021",coverURL:"https://cdn.intechopen.com/books/images_new/10384.jpg",numberOfDownloads:1310,numberOfWosCitations:0,numberOfCrossrefCitations:0,numberOfCrossrefCitationsByBook:1,numberOfDimensionsCitations:0,numberOfDimensionsCitationsByBook:1,hasAltmetrics:0,numberOfTotalCitations:0,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"July 8th 2020",dateEndSecondStepPublish:"July 29th 2020",dateEndThirdStepPublish:"September 27th 2020",dateEndFourthStepPublish:"December 16th 2020",dateEndFifthStepPublish:"February 14th 2021",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"320007",title:"Associate Prof.",name:"Muhammad",middleName:null,surname:"Zubair",slug:"muhammad-zubair",fullName:"Muhammad Zubair",profilePictureURL:"https://mts.intechopen.com/storage/users/320007/images/system/320007.png",biography:"Dr. Muhammad Zubair is an Associate Professor at the Department of Mechanical and Nuclear Engineering, University of Sharjah, United Arab Emirates. Prior to this role, Dr. Zubair worked as an assistant professor and graduate program coordinator at the University of Engineering and Technology Taxila, Pakistan.\nDr. Zubair’s interests include nuclear reactor safety, accident analysis, reliability and risk analysis, digital instrumentation and control, and radiation detection and measurements. He has a strong research background supported by publications in international journals, conferences, and book chapters. He is engaged in different research projects including one coordinated by the International Atomic Energy Agency (IAEA). He also serves as editor, associate editor, and technical committee member for international journals and conferences.",institutionString:"University of Sharjah",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"University of Sharjah",institutionURL:null,country:{name:"United Arab Emirates"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"828",title:"Reliability Engineering",slug:"reliability-engineering"}],chapters:[{id:"76775",title:"Introductory Chapter: An Overview of Reliability and Risk Analysis",doi:"10.5772/intechopen.98255",slug:"introductory-chapter-an-overview-of-reliability-and-risk-analysis",totalDownloads:214,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Muhammad Zubair and Eslam Ahmed",downloadPdfUrl:"/chapter/pdf-download/76775",previewPdfUrl:"/chapter/pdf-preview/76775",authors:[{id:"320007",title:"Associate Prof.",name:"Muhammad",surname:"Zubair",slug:"muhammad-zubair",fullName:"Muhammad Zubair"},{id:"417511",title:"Dr.",name:"Eslam",surname:"Ahmed",slug:"eslam-ahmed",fullName:"Eslam Ahmed"}],corrections:null},{id:"75481",title:"The Optimal System for Complex Series-Parallel Systems with Cold Standby Units: A Comparative Analysis Approach",doi:"10.5772/intechopen.95274",slug:"the-optimal-system-for-complex-series-parallel-systems-with-cold-standby-units-a-comparative-analysi",totalDownloads:232,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The purpose of this research is to propose three reliability models (configurations) with standby units and to study the optimum configuration between configurations analytically and numerically. The chapter considered the need for 60 MW generators in three different configurations. Configuration 1 has four 15 MW primary units, two 15 MW cold standby units and one 30 MW cold standby unit; Configuration 2 has three 20 MW primary units, three 20 cold standby units; Configuration 3 has two 30 MW primary units and three 30 MW cold standby units. Some reliability features of series–parallel systems under minor and complete failure were studied and contrasted by the current. Failure and repair time of all units is assumed to be exponentially distributed. Explanatory expressions for system characteristics such as system availability, mean time to failure (MTTF), profit function and cost benefits for all configurations have been obtained and validated by performing numerical experiments. Analysis of the effect of different system parameters on the function of profit and availability has been carried out. Analytical comparisons presented in terms of availability, mean time to failure, profit function and cost benefits have shown that configuration 3 is the optimal configuration. This is supported by numerical examples in contrast to some studies where the optimal configuration of the system is not uniform as it depends on some system parameters. Graphs and sensitivity analysis presented reveal the analytical results and accomplish that Configuration 3 is the optimal in terms of design, reliability physiognomies such as availability of the system, mean time to failure, profit and cost benefit. The study is beneficial to engineers, system designers, reliability personnel, maintenance managers, etc.",signatures:"Ibrahim Yusuf and Ismail Muhammad Musa",downloadPdfUrl:"/chapter/pdf-download/75481",previewPdfUrl:"/chapter/pdf-preview/75481",authors:[{id:"326781",title:"Associate Prof.",name:"Ibrahim",surname:"Yusuf",slug:"ibrahim-yusuf",fullName:"Ibrahim Yusuf"},{id:"326782",title:"MSc.",name:"Ismail Muhammad",surname:"Musa",slug:"ismail-muhammad-musa",fullName:"Ismail Muhammad Musa"}],corrections:null},{id:"74961",title:"Importance Analysis of Containment Spray System in Pressurized Water Reactor (PWR)",doi:"10.5772/intechopen.94412",slug:"importance-analysis-of-containment-spray-system-in-pressurized-water-reactor-pwr-",totalDownloads:330,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The basic purpose of the containment spray system (CSS) is to cool the containment atmosphere when the internal pressure of the containment exceeds a certain limit. Water is transferred by a pump from the storage tank via heat exchangers to the overhead spray nozzles in the roof of the containment. This water cools the atmosphere of the containment. In this research, the reliability analysis of CSS has been investigated using fault tree analysis (FTA). The results of the top event probabilities, minimal cut sets (MCS), risk decrease factor (RDF), risk increase factor (RIF), and sensitivity analysis were obtained for the WASH-1400 data base.",signatures:"Muhammad Zubair and Priyonta Rahman",downloadPdfUrl:"/chapter/pdf-download/74961",previewPdfUrl:"/chapter/pdf-preview/74961",authors:[{id:"320007",title:"Associate Prof.",name:"Muhammad",surname:"Zubair",slug:"muhammad-zubair",fullName:"Muhammad Zubair"},{id:"331065",title:"BSc.",name:"Priyonta",surname:"Rahman",slug:"priyonta-rahman",fullName:"Priyonta Rahman"}],corrections:null},{id:"75574",title:"Optimal Maintenance Policy for Second-Hand Equipments under Uncertainty",doi:"10.5772/intechopen.96230",slug:"optimal-maintenance-policy-for-second-hand-equipments-under-uncertainty",totalDownloads:208,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"This chapter addresses a maintenance optimization problem for re-manufactured equipments that will be reintroduced into the market as second-hand equipments. The main difference of this work and the previous literature on the maintenance optimization of second-hand equipments is the influence of the uncertainties due to the indirect obsolescence concept. The uncertainty is herein about the spare parts availability to perform some maintenance actions on equipment due to technology vanishing. The maintenance policy involves in fact a minimal repair at failure and a preventive repair after some operating period. To deal with this shortcoming, the life cycle of technology or spare parts availability is defined and modeled as a random variable whose lifetimes distribution is well known and Weibull distributed. Accordingly, an optimal maintenance policy is discussed and derived for such equipment in order to overcome the uncertainty on reparation action. Moreover, experiments are then conducted and different life cycle of technologies are evaluated according to their obsolescence processes (accidental or progressive vanishing) on the optimal operating condition.",signatures:"Ibrahima dit Bouran Sidibe, Imene Djelloul, Abdou Fane and Amadou Ouane",downloadPdfUrl:"/chapter/pdf-download/75574",previewPdfUrl:"/chapter/pdf-preview/75574",authors:[{id:"220831",title:"Dr.Ing.",name:"Ibrahima dit Bouran",surname:"Sidibe",slug:"ibrahima-dit-bouran-sidibe",fullName:"Ibrahima dit Bouran Sidibe"},{id:"222503",title:"Dr.",name:"Djelloul",surname:"Imene",slug:"djelloul-imene",fullName:"Djelloul Imene"},{id:"335208",title:"Dr.",name:"Abdou",surname:"Fane",slug:"abdou-fane",fullName:"Abdou Fane"},{id:"335209",title:"Dr.",name:"Amadou",surname:"Ouane",slug:"amadou-ouane",fullName:"Amadou Ouane"}],corrections:null},{id:"75609",title:"Digital On-Chip Calibration of Analog Systems towards Enhanced Reliability",doi:"10.5772/intechopen.96609",slug:"digital-on-chip-calibration-of-analog-systems-towards-enhanced-reliability",totalDownloads:326,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"This chapter deals with digital method of calibration for analog integrated circuits as a means of extending its lifetime and reliability, which consequently affects the reliability the analog electronic system as a whole. The proposed method can compensate for drift in circuit’s electrical parameters, which occurs either in a long term due to aging and electrical stress or it is rather more acute, being caused by process, voltage and temperature variations. The chapter reveals the implementation of ultra-low voltage on-chip system of digitally calibrated variable-gain amplifier (VGA), fabricated in CMOS 130 nm technology. It operates reliably under supply voltage of 600mV with 10% variation, in temperature range from −20°C to 85°C. Simulations suggest that the system will preserve its parameters for at least 10 years of operation. Experimental verification over 10 packaged integrated circuit (IC) samples shows the input offset voltage of VGA is suppressed in range of 13μV to 167μV. With calibration the VGA closely meets its nominally designed essential specifications as voltage gain or bandwidth. 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Tea (
There are two main varieties of the tea plant, named as
Also, on global platform it was estimated that, almost 3.8 billion gallons of tea, in which black tea has 80%, green tea 16% and remaining 4% was oolong, white and dark tea share was consumed in United States in the same year (2016) [4]. These data exhibit the ever-growing popularity of tea consumption among the masses irrespective of their region of cultivation.
The commonly found and highest content of chemical constituents found in leaves of tea are polyphenols (catechins and flavonoids), inorganic elements (e.g., fluorine, aluminum, and manganese), alkaloids (caffeine, theobromine, theophylline, etc.), amino acids, volatile oils, lipids, polysaccharide, and vitamins. However, the polyphenolic content which is present in the highest concentration, is primarily responsible for its most of the therapeutic benefits. Consequently, flavonoid contents impart its antimicrobial, antioxidant, anti-allergic and anti-inflammatory effects. The phenolic content variants are further elaborated and sub-classified as catechin, gallocatechin, epigallocatechin, epicatechin gallate, epicatechin, and epigallocatechin-gallate (EGCG), the latter being the most active component [2, 5]. Further, the molecular structure of green tea polyphenols exhibits active hydroxyl hydrogen which effectively scavenge free radicals hence, slowing down the detrimental changes in most of the physiological processes existing in human body. Reportedly, tea polyphenols strongly exhibits the movement of glutathione peroxidase and superoxide dismutase causing higher scavenging rate. The phytoconstituents of tea reflects multiple therapeutic benefits on our various diverse physiological systems through various biochemical and pharmacological processes like—antioxidant activities, inhibition of cell proliferation, induction of apoptosis, cell cycle arrest and modulation of carcinogen metabolism [6, 7]. Similarly, in CNS, another constituent in green tea, L-theanine increases the dopamine and serotonin levels resulting in mood elevation and stress reduction. Also, caffeine content in same sources aids in increasing the focus, vigilance, concentration and reasoning ability [8]. Theobromine and theophylline are known as potential CNS stimulants. Numerous studies have shown that most of the tea polyphenols have reactive oxygen and nitrogen species (ROS) scavenging activity along with an ability to chelate down redox-active transition metal ions. Currently, apart from all the listed health benefits exhibited by the tea and its polyphenols, the focus is towards exploring its chemo preventive, hypolipidemic and anti-obesity effects in all sorts of possible
Tea leaves are either classified on the basis of their consumption and texture it has or on the processing method adopted for their leaves. Hence, the classification, studied commonly for tea is based on its varied fermentation degree process and is comprised of basically three types: non-fermented (green), semi-fermented (oolong) and entirely fermented (black) [10]. The tea processing starts firstly, from picking up the appropriate and selected tea leaves from shrub or tea tree which undergoes fractional withering. Then roasting the same leaves to inactivate oxidative enzymes, followed by rolling up, drying and sorting the same leaves. The color of the final tea product is usually green tasting slightly constringent. So many countries like China, the taste of green tea is improvised by supplementing aromatic fruits (orange) or flowers (jasmine). Further, the tea processing steps in case of black tea is more complex, as after withering process the tea leaves are subjected for two steps fermentation processes, in the last step of fermentation they have been rolled up and then fermented. Lastly, they are roasted till they become dark-brown or brown black in color imparting a roasting aroma so as to block the activity of enzymes (polyphenol oxidase and glycosidase) along with further, fermentation of the same [5]. Another variant, oolong tea which is partially fermented type usually has shorter fermentation time in comparison to the black one.
Green tea is a non-fermented tea which is largely consumed by the population of china and japan. After cultivation, tea leaves are first withered for the inactivation of enzyme (polyphenol) which is liable for oxidation of tea catechins into their oligomeric forms (thearubigins and theaflavins). To avoid the oxidation and polymerization of tea leaves, they are steamed up and dried at high temperatures [6, 9, 11]. The Chinese traditional dietary system do have another packed form of green tea called “black powder”, named after type of leaves processing method. Where these leaves individually are stirred and wrapped into a round pellet looking like explosives. It prevents it from any kind of physical damage and maintains its fragrance and flavor. Polyphenols present in green tea are flavonols (quercetin, kaempferol, and rutin), caffeine, phenolic acids, theanine, flavor, and leucoanthocyanins, which show 40% of dry weight of leaves [12, 13]. The highly water-soluble parts of tea comprises of biochemical components like (−) epigallocatechin-3-gallate (EGCG), epigallocatechin (EGC), epicatechin-3-gallate (ECG), and epicatechin (EC) (As listed in Table 1) [9, 14]. Further, it’s also been reported that 1 kg of green tea has around 191 g of the above listed catechins, 36 g of caffeine, and 5.2 g of flavonols [15]. In green tea there are 10–15% of polyphenols present whereas it’s lesser in black tea, i.e. around 5%. Dry weight of green tea constitutes about 42% polyphenols which is composed of 26.7% of catechin-gallate components such as ECG (2.25%), EGC (10.32%), Catechins (0.53%), EGCG (11.16%) and Epicatechin (2.45%) [16]. It’s been estimated that in one cup of green tea the expected concentration of EGCG is between 2.1–2.4 mg/mL and after testing the effects of both Green tea and EGCG (equivalent of 4–8 cups per day) on human subjects there was no appreciable side effects observed [17, 18]. Epidemiological studies too, have suggested protective and suppressive effects against many types of human cancer (including that of skin, lung, liver, esophagus, and stomach) after tea consumption [19, 20, 21].
Representing the types and structure of phytocompounds present in the green tea with their therapeutic benefits.
This variety of tea is very famous in North America, Europe, and India. Black tea is extracted from the new, soft, firstly appeared leaves of
Representing the types and structure of phytocompounds present in the black tea with their therapeutic benefits.
Oolong tea is a conventional Chinese tea with a different, unique production method and one of the most popular beverages in china with its Chinese name meaning as “Black dragon tea”. It is a semi fermented tea with restricted time of oxidation as compared to black tea and contains phytocompounds of both black and green tea. It has approximately half of the EGCG from green tea, while double quantity of polymerized polyphenols and theaflavins of black tea. The procyanidins produced in oolong tea are formed due to its unique fermentation process. The leaves are first withered, sun dried and then allowed for oxidation before rolling and twisting.
As all tea leaves are green when they are plucked. Green tea undergoes, heating process in order to inhibit the oxidation of tea leaves. They are rolled up to break the cell structure. While, oolong tea is plucked and kept in optimized condition and allowed for oxidation. Due to difference in its processing method oolong tea tastes different from its sub varieties. It shows a sweet and fruity flavor with striking honey odors to woody and dense with roasted aromas, or even green and fresh with flowery aromas. They are processed by different methods as some are wrapped-curled into small beads and others are rolled into curly leaves. In china, oolong tea is added with flavors like jasmine flowers (Tables 3 and 4) [32].
Representing the types and structure of phytocompounds present in the oolong tea with their therapeutic benefits.
Polyphenols | Chemical structure | Oolong tea phytocompound concentration (mg/g) | Green tea phytocompound concentration (mg/g) |
---|---|---|---|
Caffeine | C8H10N4O2 | 64 | 53 |
Catechin | C15H14O6 | 30 | 43 |
Epicatechin | C15H14O6 | 6 | 25 |
Gallocatechin | C15H14O7 | 10 | 5 |
Epigallocatechin | C15H14O7 | 2 | 8 |
Epigallocatechin gallate | C22H18O11 | 14 | 29 |
Gallocatechin gallate | C22H18O11 | 16 | 19 |
Epicatechin gallate | C22H18O11 | 3 | 6 |
Catechin gallate | C22H18O10 | 7 | 5 |
114 | – |
Comparing the polyphenolic contents of oolong and green tea.
As discussed earlier, the health-promoting properties of the tea plants are often credited to their active ingredients including polyphenols. Tea flavanols are a group of natural polyphenols (epicatechins) found in most of the varieties of tea. Their therapeutic benefits although are immense, but they do have contributed exclusively in neural health of living beings. Likewise, the polyphenols of green tea are reported extensively in preventing neuronal degradation by inhibiting neurotoxin formation in cells [33, 34]. Also, in one of the recent study done, with transitional metal (iron and copper) chelating property or EGCG, suggested its possible effective role in treating certain forms of neurodegenerative diseases. Similarly, the antioxidative property of EGCG exhibits protection against advanced glycation end products (AGEs) induced neuronal cells injury along with inhibit AGEs—AGE receptor (RAGE) interaction intervened pathways, suggesting a possible therapeutic role of tea catechins for neurodegenerative diseases. Hence, both black and green tea varieties are reported to contribute immensely for the protection against neurodegenerative diseases [34, 35, 36]. Also, oxidative variations of cellular components such as nucleic acids, lipids, and proteins are prevented by bidirectional antioxidative property [37]. The oxidation of these components in aqueous phase is responsible for initiation of membrane lipid peroxidation [35].
Moreover, these water soluble tea polyphenols, particularly catechins have effective potential to scavenge free radicals and reduce the versatility of free radicals in the lipid structures too. Polyphenols enters the phospholipids bilayer, coating it with film and, balancing out the impact, by adjusting the lipid pressing ability [38]. They also contain higher amount of chemically dynamic metal particles (iron and copper) creating
Due to the existence of hydroxyl ions on polyphenol ring metal chelation effects can be observed. Metal Chelating effects by Green and Black Tea additionally, restricts lipid per oxidation and secures the essential lipid structures present in cerebrum leading to reduce oxidative stress [10, 27, 41]. Furthermore, it’s been observed in research studies that the phytocompounds of tea (Green/Black) also prevents, the division of mitochondrial layer against iron induced lipid per oxidation and enhanced the survival rate in many
One of the essential pathological cause in Alzheimer’s disease (AD) is irregular contact of free chelatable iron which is responsible for the deposition of neocortical amyloid peptide and deposition of metals, phosphorylation of tau and formation of tangles due to production of tau protein from microtubules [45, 46]. Also, the activation of amyloid cascades, which produces amyloid by β-amyloid precursor protein (APP), accumulates in the presence of divalent metal ions into amyloid fibrils leading to a major cause of AD [47, 48].
Recent studies have reported that the delay in onset or slowdown of the neurodegenerative process along with minimal neural deterioration was observed in the population consuming tea infusions on regular basis [49]. There scientific correlation suggests that the reduction in amyloid beta (Aβ) fibril production in the presence of EC and EGCG is suspected to regulate the amyloid protein precursor (APP) enzyme activity [50]. Additionally, it been also suggested that the regular consumption of tea (green and black) may lead to the acetyl cholinesterase (AChE) activity inhibition, further causing halt in acetylcholine production [51, 52]. Besides this, it was found that there was inhibition of butyrylcholinesterase (BuChE) enzyme deposits in the brain of AD subjects after consuming green tea or black tea for certain time [53]. These research findings advices that active phytocompounds present in tea can be used to obstruct the development of AD [54].
Tachibana et al. [55] studied the effect of tea polyphenols, and suggested that EGCG directly binds to the Laminin receptor (67LR), located on the peptide LR161-170. This receptor shows a high expression only in cancerous cells. This suggests that EGCG specifically binds to the cancer cells and binding of EGCG with 67LR receptor activate the enzyme protein kinase B which further activate ENOS pathway leading to vasodilation that contributes to the improvement of cardiovascular function of cell [16, 55]. It also elevates the activity of CGMP that activate the PKC/Acidic sphingomyelinases that induces the apoptosis in cancerous cells.
Nozawa et al. [56] discovered the death of 50% of neurons at higher concentration of glutamate but when pre-treated with theanine, the possibility of death was significantly decreased. Many more recent updates suggested that increased glutamate level in cell may lead to massive influx of Ca+ ions and increases the formation of ROS which leads to the death of neuronal cells. In order to avoid the toxicity of glutamate, the glutamate receptors binds with theanine. Theanine has same structure as glutamate so in presence of theanine it shows a competitive inhibition and inhibit the binding of glutamate to its receptor. Furthermore, Kakuda et al. [57] studies the inhibiting effect of glutamate receptors by theanine that suggests the neuroprotective role of theanine. It shows the specific binding of theanine to NMDA receptor to inhibit the glutamate binding affinity. Theanine has an antagonistic effect to glutamate receptors. Glutamine, derived from glutamate, is synthesized by glutamine synthetase. Theanine can inhibit the transport of glutamine and regulate the glutamate-glutamine cycle in the neurons and, thus, shows the neuroprotective effect of tea (Figure 1) [58].
Schematic representation. Inhibition effect of theanine on glutamate receptor.
Although being therapeutically crucial compound tea phytocompounds do have certain harmful side effects, if over consumed or overdosed like—higher Caffeine content, Aluminum presence and the effects of tea polyphenols on iron bioavailability [59, 60]. In the study done by Lin et al. [31], it was been reported that the caffeine content in tea is available in following order: black tea > oolong tea > green tea > fresh tea leaf. Similarly, Cabrera et al. also studied the caffeine content and its after effects in 45 samples of tea and determined that black tea has the high concentration of caffeine (41.5–67.4 mg/g), whereas oolong and green tea samples have less amount of caffeine content of 32.5 and 29.2 mg/g, respectively [61]. The harmful effects of caffeine content in tea are listed as—vomiting, sleep disorder, nervousness, tachycardia, and epigastric pain etc. [62]. Hence, tea intake is strictly restricted in patients suffering from cardiovascular problems. Breastfeeding and pregnant women should avoid over-consumption of green tea because it do causes tachycardia in them giving rise to higher health risks to fetus [63, 64]. The presence of aluminum in black and green teas also suggested increased accumulation of the same inside the body affecting the neural well-being and causing neurological disorders [65].
It can be concluded in the review that tea polyphenols with other constituents have a very high therapeutic potential including the potency to decrease the threat of diseases such as cancer, cardiovascular, diabetes and neurodegenerative diseases. It has proven to be a strong antioxidant agent that shows a therapeutic effect of tea. To evaluate the efficacy of tea many experiments are being conducted which shows a promising data from many trials and other ongoing trials are conducted to study the therapeutic effect of tea. Because less information is available about bioavailability of tea polyphenols after intake of tea, studies of bioavailability polyphenols of tea is needed on animals and humans to evaluate its protective role.
Microbes are ubiquitous in nature and humans are no exception. Microbes have coevolved with humans and reside in and on human body to develop a host associated structure, called “Human Microbiome” or “Human Microbiota.” These microbial counterparts account toward 10% of human body weight and outnumber human cells by approximately by tenfold and considered as commensals. Human microbiome is defined as the total genomes of microbes (constitute bacteria, bacteriophage, fungi, protozoa and viruses) that live inside or on the human body [1]. There are trillions of microbes living in/on human body plays a fundamental role in normal functioning of metabolic, physiological and immune system. Microbiota is a complex ecosystem consisting of bacteria, protozoa, viruses and fungi; all varies in number even in body parts of same individual. Human body has 10 times more bacteria than the number of human cells in our body [2]. Most of these bacteria are present in gastrointestinal tract [3] which account for approximate 70% of the total microbial load in or on human body (particular in large intestine) [4]. Humans are born sterile and start acquiring human companion to shape resilient microbiome structure. Establishment of microbiome starts with birth and matures with age. Microbial introduction and the establishment of microbiome is a random process influenced by many factor like mode of delivery, diet, sex, age, genetics, geographical location have a strong impact in shaping human microbiome structure [5, 6, 7, 8, 9, 10]. These microbes are in symbiotic relationship, beside gut they are also found in mouth, respiratory tract, vagina and skin.
The study of human microbiome diversity started with Antonie Van Leeuwenhoek, when he had a comparison of his oral and fecal microbiota in 1680s. He found that different microbes are present in different habitats and also different microbes are present in healthy and diseased person [11, 12]. There is a growing evidence that any change in microbiota composition leads to several metabolic diseases including obesity, diabetes and cardiovascular. Different parts of intestinal tract have different composition of microbes and it varies according to age, weight, site and diet. Composition of microbiota in gut alters by nutrition, drugs, diet and genetic background and lifestyle. Microbiota regulates metabolic and physiological mechanisms by producing metabolites. It has been found out that different species of microbiota in gut works under same metabolic pathway [9]. Qualitative and quantitative alteration in gut microbiota leads to dysbiosis by consuming antibiotics, physical and psychological stress [13]. Recent studies shows evidence regarding change in composition by urban and rural environment, affects skin (allergic symptoms) of particular organisms. Age alter the environmental effects on individual such as alter microbiota variations in skin between children and teenager cause skin allergies [14]. Microbiome structure varies in respect of host anatomical and physiological sites. Normally, flora found in/on the body surface in stable condition to compete with pathogenic microbes in environment or those microbes entered in specific body parts [15]. As in addition to these permanent residents, a number of microbes known as causative agent for various infectious diseases. Likewise commensals, these infectious agents have evolved an efficient machinery to evade host protective gears for their successful proliferation in various anatomical locations. Normal bacteria defend host against the invasion of pathogenic microorganisms by inducing barrier against them [16]. It was observed that host commensals plays a critical role in balancing the abundance of pathogenic and nonpathogenic microbial strains and protects the host form the onset of any infectious diseases. However a number of factors like change in diet, variable host immune response, fluctuating environmental conditions like pH, oxygen saturation, ionic strength, etc., could induce microbial dysbiosis and induce microbial community dynamics. These microbial community dynamics could induce favorable conditions for growth of earlier dormant pathogenic microbes and result in onset of infectious diseases [16].
Microbes have been identified to play a vital role in human health and diseases. Physiological characterization of these microbes and defining their functional molecular machinery could enable us to develop potential therapeutic and diagnostic targets. Additionally, holistic overview of human microbiome structure, human microbe interactions and role of microbes in human health and diseases are the key areas of current research focus. In-depth information about host microbial interaction in human health and diseases could enable to identify causative factors for development of host physiological/metabolic disorders. Current book comprises of various chapters defining a relation among human and microbes in health and diseases.
IntechOpen aims to guarantee that original material is published while at the same time giving significant freedom to our Authors. We uphold a flexible Copyright Policy, guaranteeing that there is no transfer of copyright to the publisher and Authors retain exclusive copyright to their Work.
',metaTitle:"Publication Agreement - Monograph",metaDescription:"IntechOpen aims to guarantee that original material is published while at the same time giving significant freedom to our authors. For that matter, we uphold a flexible copyright policy meaning that there is no transfer of copyright to the publisher and authors retain exclusive copyright to their work.",metaKeywords:null,canonicalURL:"/page/publication-agreement-monograph",contentRaw:'[{"type":"htmlEditorComponent","content":"When submitting a manuscript, the Author is required to accept the Terms and Conditions set out in our Publication Agreement – Monographs/Compacts as follows:
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\\n\\nIntechOpen has the right to include/use the Author and Co-Authors names and likeness in connection with scientific dissemination, retrieval, archiving, web hosting and promotion and marketing of the Work and has the right to contact the Author and Co-Authors until the Work is publicly available on any platform owned and/or operated by IntechOpen.
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\\n\\nThird Party Rights: A person who is not a party to this Publication Agreement may not enforce any of its provisions under the Contracts (Rights of Third Parties) Act 1999.
\\n\\nEntire Agreement: This Publication Agreement constitutes the entire agreement between the parties in relation to its subject matter. It replaces all prior agreements, draft agreements, arrangements, collateral warranties, collateral contracts, statements, assurances, representations and undertakings of any nature made by, or on behalf of, the parties, whether oral or written, in relation to that subject matter. Each party acknowledges that in entering into this Publication Agreement it has not relied upon any oral or written statements, collateral or other warranties, assurances, representations or undertakings which were made by or on behalf of the other party in relation to the subject matter of this Publication Agreement at any time before its signature (known as the "Pre-Contractual Statements"), other than those which are set out in this Publication Agreement. Each party hereby waives all rights and remedies which might otherwise be available to it in relation to such Pre-Contractual Statements. Nothing in this clause shall exclude or restrict the liability of either party arising out of any fraudulent pre-contract misrepresentation or concealment.
\\n\\nWaiver: No failure or delay by a party to exercise any right or remedy provided under this Publication Agreement or by law shall constitute a waiver of that or any other right or remedy, nor shall it preclude or restrict the further exercise of that or any other right or remedy. No single or partial exercise of such right or remedy shall preclude or restrict the further exercise of that or any other right or remedy.
\\n\\nVariation: No variation of this Publication Agreement shall have effect unless it is in writing and signed by the parties, or their duly authorized representatives.
\\n\\nSeverance: If any provision, or part-provision, of this Publication Agreement is, or becomes invalid, illegal or unenforceable, it shall be deemed modified to the minimum extent necessary to make it valid, legal and enforceable. If such modification is not possible, the relevant provision or part-provision shall be deemed deleted. Any modification to, or deletion of, a provision or part-provision under this clause shall not affect the validity and enforceability of the rest of this Publication Agreement.
\\n\\nNo partnership: Nothing in this Publication Agreement is intended to, or shall be deemed to, establish or create any partnership or joint venture or the relationship of principal and agent or employer and employee between IntechOpen and the Author or any Co-Author, nor authorize any party to make or enter into any commitments for, or on behalf of, any other party.
\\n\\nGoverning law: This Publication Agreement and any dispute or claim, including non-contractual disputes or claims arising out of, or in connection with it, or its subject matter or formation, shall be governed by and construed in accordance with the law of England and Wales. The parties submit to the exclusive jurisdiction of the English courts to settle any dispute or claim arising out of, or in connection with, this Publication Agreement, including any non-contractual disputes or claims.
\\n\\nPolicy last updated: 2018-09-11
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\n\nCORRESPONDING AUTHOR'S GRANT OF RIGHTS
\n\nSubject to the following Article, the Author grants to IntechOpen, during the full term of copyright, and any extensions or renewals of that term, the following:
\n\nThe foregoing licenses shall survive the expiry or termination of this Publication Agreement for any reason.
\n\nThe Author, on his or her own behalf and on behalf of any of the Co-Authors, reserves the following rights in the Work but agrees not to exercise them in such a way as to adversely affect IntechOpen's ability to utilize the full benefit of this Publication Agreement: (i) reprographic rights worldwide, other than those which subsist in the typographical arrangement of the Work as published by IntechOpen; and (ii) public lending rights arising under the Public Lending Right Act 1979, as amended from time to time, and any similar rights arising in any part of the world.
\n\nThe Author, and any Co-Author, confirms that they are, and will remain, a member of any applicable licensing and collecting society and any successor to that body responsible for administering royalties for the reprographic reproduction of copyright works.
\n\nSubject to the license granted above, copyright in the Work and all versions of it created during IntechOpen's editing process, including all published versions, is retained by the Author and any Co-Authors.
\n\nSubject to the license granted above, the Author and Co-Authors retain patent, trademark and other intellectual property rights to the Work.
\n\nAll rights granted to IntechOpen in this Article are assignable, sublicensable or otherwise transferrable to third parties without the specific approval of the Author or Co-Authors.
\n\nThe Author, on his/her own behalf and on behalf of the Co-Authors, will not assert any rights under the Copyright, Designs and Patents Act 1988 to object to derogatory treatment of the Work as a consequence of IntechOpen's changes to the Work arising from the translation of it, corrections and edits for house style, removal of problematic material and other reasonable edits as determined by IntechOpen.
\n\nAUTHOR'S DUTIES
\n\nWhen distributing or re-publishing the Work, the Author agrees to credit the Monograph/Compacts as the source of first publication, as well as IntechOpen. The Author guarantees that Co-Authors will also credit the Monograph/Compacts as the source of first publication, as well as IntechOpen, when they are distributing or re-publishing the Work.
\n\nThe Author agrees to:
\n\nThe Author will be held responsible for the payment of the agreed Open Access Publishing Fee before the completion of the project (Monograph/Compacts publication).
\n\nAll payments shall be due 30 days from the date of issue of the invoice. The Author or whoever is paying on behalf of the Author and Co-Authors will bear all banking and similar charges incurred.
\n\nThe Author shall obtain in writing all consents necessary for the reproduction of any material in which a third-party right exists, including quotations, photographs and illustrations, in all editions of the Work worldwide for the full term of the above licenses, and shall provide to IntechOpen, at its request, the original copies of such consents for inspection or the photocopies of such consents.
\n\nThe Author shall obtain written informed consent for publication from those who might recognize themselves or be identified by others, for example from case reports or photographs.
\n\nThe Author shall respect confidentiality during and after the termination of this Agreement. The information contained in all correspondence and documents as part of the publishing activity between IntechOpen and the Author and Co-Authors are confidential and are intended only for the recipients. The contents of any communication may not be disclosed publicly and are not intended for unauthorized use or distribution. Any use, disclosure, copying, or distribution is prohibited and may be unlawful.
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\n\nThe Author and Co-Authors confirm and warrant that the Work does not and will not breach any applicable law or the rights of any third party and, specifically, that the Work contains no matter that is defamatory or that infringes any literary or proprietary rights, intellectual property rights, or any rights of privacy.
\n\nThe Author and Co-Authors confirm that: (i) the Work is their original work and is not copied wholly or substantially from any other work or material or any other source; (ii) the Work has not been formally published in any other peer-reviewed journal or in a book or edited collection, and is not under consideration for any such publication; (iii) Authors and any applicable Co-Authors are qualifying persons under section 154 of the Copyright, Designs and Patents Act 1988; (iv) Authors and any applicable Co-Authors have not assigned, and will not during the term of this Publication Agreement purport to assign, any of the rights granted to IntechOpen under this Publication Agreement; and (v) the rights granted by this Publication Agreement are free from any security interest, option, mortgage, charge or lien.
\n\nThe Author and Co-Authors also confirm and warrant that: (i) he/she has the power to enter into this Publication Agreement on his or her own behalf and on behalf of each Co-Author; and (ii) has the necessary rights and/or title in and to the Work to grant IntechOpen, on behalf of themselves and any Co-Author, the rights and licences in this Publication Agreement. If the Work was prepared jointly by the Author and Co-Authors, the Author confirms that: (i) all Co-Authors agree to the submission, license and publication of the Work on the terms of this Publication Agreement; and (ii) the Author has the authority to enter into this biding Publication Agreement on behalf of each Co-Author. The Author shall: (i) ensure each Co-Author complies with all relevant provisions of this Publication Agreement, including those relating to confidentiality, performance and standards, as if a party to this Publication Agreement; and (ii) remain primarily liable for all acts and/or omissions of each Co-Author.
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\n\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen, at its discretion, agrees to publish the Work attributing it to the Author and Co-Authors.
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\n\nIntechOpen is granted the authority to enforce the rights from this Publication Agreement on behalf of the Author and Co-Authors against third parties, for example in cases of plagiarism or copyright infringements. In respect of any such infringement or suspected infringement of the copyright in the Work, IntechOpen shall have absolute discretion in addressing any such infringement that is likely to affect IntechOpen's rights under this Publication Agreement, including issuing and conducting proceedings against the suspected infringer.
\n\nIntechOpen has the right to include/use the Author and Co-Authors names and likeness in connection with scientific dissemination, retrieval, archiving, web hosting and promotion and marketing of the Work and has the right to contact the Author and Co-Authors until the Work is publicly available on any platform owned and/or operated by IntechOpen.
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\n\nFurther Assurance: The Author shall ensure that any relevant third party, including any Co-Author, shall execute and deliver whatever further documents or deeds and perform such acts as IntechOpen reasonably requires from time to time for the purpose of giving IntechOpen the full benefit of the provisions of this Publication Agreement.
\n\nThird Party Rights: A person who is not a party to this Publication Agreement may not enforce any of its provisions under the Contracts (Rights of Third Parties) Act 1999.
\n\nEntire Agreement: This Publication Agreement constitutes the entire agreement between the parties in relation to its subject matter. It replaces all prior agreements, draft agreements, arrangements, collateral warranties, collateral contracts, statements, assurances, representations and undertakings of any nature made by, or on behalf of, the parties, whether oral or written, in relation to that subject matter. Each party acknowledges that in entering into this Publication Agreement it has not relied upon any oral or written statements, collateral or other warranties, assurances, representations or undertakings which were made by or on behalf of the other party in relation to the subject matter of this Publication Agreement at any time before its signature (known as the "Pre-Contractual Statements"), other than those which are set out in this Publication Agreement. Each party hereby waives all rights and remedies which might otherwise be available to it in relation to such Pre-Contractual Statements. Nothing in this clause shall exclude or restrict the liability of either party arising out of any fraudulent pre-contract misrepresentation or concealment.
\n\nWaiver: No failure or delay by a party to exercise any right or remedy provided under this Publication Agreement or by law shall constitute a waiver of that or any other right or remedy, nor shall it preclude or restrict the further exercise of that or any other right or remedy. No single or partial exercise of such right or remedy shall preclude or restrict the further exercise of that or any other right or remedy.
\n\nVariation: No variation of this Publication Agreement shall have effect unless it is in writing and signed by the parties, or their duly authorized representatives.
\n\nSeverance: If any provision, or part-provision, of this Publication Agreement is, or becomes invalid, illegal or unenforceable, it shall be deemed modified to the minimum extent necessary to make it valid, legal and enforceable. If such modification is not possible, the relevant provision or part-provision shall be deemed deleted. Any modification to, or deletion of, a provision or part-provision under this clause shall not affect the validity and enforceability of the rest of this Publication Agreement.
\n\nNo partnership: Nothing in this Publication Agreement is intended to, or shall be deemed to, establish or create any partnership or joint venture or the relationship of principal and agent or employer and employee between IntechOpen and the Author or any Co-Author, nor authorize any party to make or enter into any commitments for, or on behalf of, any other party.
\n\nGoverning law: This Publication Agreement and any dispute or claim, including non-contractual disputes or claims arising out of, or in connection with it, or its subject matter or formation, shall be governed by and construed in accordance with the law of England and Wales. The parties submit to the exclusive jurisdiction of the English courts to settle any dispute or claim arising out of, or in connection with, this Publication Agreement, including any non-contractual disputes or claims.
\n\nPolicy last updated: 2018-09-11
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Kasenga",hash:"91cde4582ead884cb0f355a19b67cd56",volumeInSeries:4,fullTitle:"Malaria",editors:[{id:"86725",title:"Dr.",name:"Fyson",middleName:"Hanania",surname:"Kasenga",slug:"fyson-kasenga",fullName:"Fyson Kasenga",profilePictureURL:"https://mts.intechopen.com/storage/users/86725/images/system/86725.jpg",institutionString:"Malawi Adventist University",institution:{name:"Malawi Adventist University",institutionURL:null,country:{name:"Malawi"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null},{type:"book",id:"7123",title:"Current Topics in Neglected Tropical Diseases",subtitle:null,coverURL:"https://cdn.intechopen.com/books/images_new/7123.jpg",slug:"current-topics-in-neglected-tropical-diseases",publishedDate:"December 4th 2019",editedByType:"Edited by",bookSignature:"Alfonso J. Rodriguez-Morales",hash:"61c627da05b2ace83056d11357bdf361",volumeInSeries:3,fullTitle:"Current Topics in Neglected Tropical Diseases",editors:[{id:"131400",title:"Prof.",name:"Alfonso J.",middleName:null,surname:"Rodriguez-Morales",slug:"alfonso-j.-rodriguez-morales",fullName:"Alfonso J. Rodriguez-Morales",profilePictureURL:"https://mts.intechopen.com/storage/users/131400/images/system/131400.png",institutionString:"Institución Universitaria Visión de las Américas, Colombia",institution:null}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null},{type:"book",id:"7064",title:"Current Perspectives in Human Papillomavirus",subtitle:null,coverURL:"https://cdn.intechopen.com/books/images_new/7064.jpg",slug:"current-perspectives-in-human-papillomavirus",publishedDate:"May 2nd 2019",editedByType:"Edited by",bookSignature:"Shailendra K. Saxena",hash:"d92a4085627bab25ddc7942fbf44cf05",volumeInSeries:2,fullTitle:"Current Perspectives in Human Papillomavirus",editors:[{id:"158026",title:"Prof.",name:"Shailendra K.",middleName:null,surname:"Saxena",slug:"shailendra-k.-saxena",fullName:"Shailendra K. Saxena",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRET3QAO/Profile_Picture_2022-05-10T10:10:26.jpeg",institutionString:"King George's Medical University",institution:{name:"King George's Medical University",institutionURL:null,country:{name:"India"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null}]},subseriesFiltersForPublishedBooks:[{group:"subseries",caption:"Bacterial Infectious Diseases",value:3,count:2},{group:"subseries",caption:"Parasitic Infectious Diseases",value:5,count:4},{group:"subseries",caption:"Viral Infectious Diseases",value:6,count:7}],publicationYearFilters:[{group:"publicationYear",caption:"2022",value:2022,count:2},{group:"publicationYear",caption:"2021",value:2021,count:4},{group:"publicationYear",caption:"2020",value:2020,count:3},{group:"publicationYear",caption:"2019",value:2019,count:3},{group:"publicationYear",caption:"2018",value:2018,count:1}],authors:{paginationCount:303,paginationItems:[{id:"280338",title:"Dr.",name:"Yutaka",middleName:null,surname:"Tsutsumi",slug:"yutaka-tsutsumi",fullName:"Yutaka Tsutsumi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/280338/images/7961_n.jpg",biography:null,institutionString:null,institution:{name:"Fujita Health University",country:{name:"Japan"}}},{id:"116250",title:"Dr.",name:"Nima",middleName:null,surname:"Rezaei",slug:"nima-rezaei",fullName:"Nima Rezaei",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/116250/images/system/116250.jpg",biography:"Professor Nima Rezaei obtained an MD from Tehran University of Medical Sciences, Iran. He also obtained an MSc in Molecular and Genetic Medicine, and a Ph.D. in Clinical Immunology and Human Genetics from the University of Sheffield, UK. He also completed a short-term fellowship in Pediatric Clinical Immunology and Bone Marrow Transplantation at Newcastle General Hospital, England. Dr. Rezaei is a Full Professor of Immunology and Vice Dean of International Affairs and Research, at the School of Medicine, Tehran University of Medical Sciences, and the co-founder and head of the Research Center for Immunodeficiencies. He is also the founding president of the Universal Scientific Education and Research Network (USERN). Dr. Rezaei has directed more than 100 research projects and has designed and participated in several international collaborative projects. He is an editor, editorial assistant, or editorial board member of more than forty international journals. He has edited more than 50 international books, presented more than 500 lectures/posters in congresses/meetings, and published more than 1,100 scientific papers in international journals.",institutionString:"Tehran University of Medical Sciences",institution:{name:"Tehran University of Medical Sciences",country:{name:"Iran"}}},{id:"180733",title:"Dr.",name:"Jean",middleName:null,surname:"Engohang-Ndong",slug:"jean-engohang-ndong",fullName:"Jean Engohang-Ndong",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/180733/images/system/180733.png",biography:"Dr. Jean Engohang-Ndong was born and raised in Gabon. After obtaining his Associate Degree of Science at the University of Science and Technology of Masuku, Gabon, he continued his education in France where he obtained his BS, MS, and Ph.D. in Medical Microbiology. He worked as a post-doctoral fellow at the Public Health Research Institute (PHRI), Newark, NJ for four years before accepting a three-year faculty position at Brigham Young University-Hawaii. Dr. Engohang-Ndong is a tenured faculty member with the academic rank of Full Professor at Kent State University, Ohio, where he teaches a wide range of biological science courses and pursues his research in medical and environmental microbiology. Recently, he expanded his research interest to epidemiology and biostatistics of chronic diseases in Gabon.",institutionString:"Kent State University",institution:{name:"Kent State University",country:{name:"United States of America"}}},{id:"188773",title:"Prof.",name:"Emmanuel",middleName:null,surname:"Drouet",slug:"emmanuel-drouet",fullName:"Emmanuel Drouet",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/188773/images/system/188773.png",biography:"Emmanuel Drouet, PharmD, is a Professor of Virology at the Faculty of Pharmacy, the University Grenoble-Alpes, France. As a head scientist at the Institute of Structural Biology in Grenoble, Dr. Drouet’s research investigates persisting viruses in humans (RNA and DNA viruses) and the balance with our host immune system. He focuses on these viruses’ effects on humans (both their impact on pathology and their symbiotic relationships in humans). He has an excellent track record in the herpesvirus field, and his group is engaged in clinical research in the field of Epstein-Barr virus diseases. He is the editor of the online Encyclopedia of Environment and he coordinates the Universal Health Coverage education program for the BioHealth Computing Schools of the European Institute of Science.",institutionString:null,institution:{name:"Grenoble Alpes University",country:{name:"France"}}},{id:"131400",title:"Prof.",name:"Alfonso J.",middleName:null,surname:"Rodriguez-Morales",slug:"alfonso-j.-rodriguez-morales",fullName:"Alfonso J. Rodriguez-Morales",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/131400/images/system/131400.png",biography:"Dr. Rodriguez-Morales is an expert in tropical and emerging diseases, particularly zoonotic and vector-borne diseases (especially arboviral diseases). He is the president of the Travel Medicine Committee of the Pan-American Infectious Diseases Association (API), as well as the president of the Colombian Association of Infectious Diseases (ACIN). He is a member of the Committee on Tropical Medicine, Zoonoses, and Travel Medicine of ACIN. He is a vice-president of the Latin American Society for Travel Medicine (SLAMVI) and a Member of the Council of the International Society for Infectious Diseases (ISID). Since 2014, he has been recognized as a Senior Researcher, at the Ministry of Science of Colombia. He is a professor at the Faculty of Medicine of the Fundacion Universitaria Autonoma de las Americas, in Pereira, Risaralda, Colombia. He is an External Professor, Master in Research on Tropical Medicine and International Health, Universitat de Barcelona, Spain. He is also a professor at the Master in Clinical Epidemiology and Biostatistics, Universidad Científica del Sur, Lima, Peru. In 2021 he has been awarded the “Raul Isturiz Award” Medal of the API. Also, in 2021, he was awarded with the “Jose Felix Patiño” Asclepius Staff Medal of the Colombian Medical College, due to his scientific contributions to COVID-19 during the pandemic. He is currently the Editor in Chief of the journal Travel Medicine and Infectious Diseases. His Scopus H index is 47 (Google Scholar H index, 68).",institutionString:"Institución Universitaria Visión de las Américas, Colombia",institution:null},{id:"332819",title:"Dr.",name:"Chukwudi Michael",middleName:"Michael",surname:"Egbuche",slug:"chukwudi-michael-egbuche",fullName:"Chukwudi Michael Egbuche",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/332819/images/14624_n.jpg",biography:"I an Dr. Chukwudi Michael Egbuche. I am a Senior Lecturer in the Department of Parasitology and Entomology, Nnamdi Azikiwe University, Awka.",institutionString:null,institution:{name:"Nnamdi Azikiwe University",country:{name:"Nigeria"}}},{id:"284232",title:"Mr.",name:"Nikunj",middleName:"U",surname:"Tandel",slug:"nikunj-tandel",fullName:"Nikunj Tandel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/284232/images/8275_n.jpg",biography:'Mr. Nikunj Tandel has completed his Master\'s degree in Biotechnology from VIT University, India in the year of 2012. He is having 8 years of research experience especially in the field of malaria epidemiology, immunology, and nanoparticle-based drug delivery system against the infectious diseases, autoimmune disorders and cancer. He has worked for the NIH funded-International Center of Excellence in Malaria Research project "Center for the study of complex malaria in India (CSCMi)" in collaboration with New York University. The preliminary objectives of the study are to understand and develop the evidence-based tools and interventions for the control and prevention of malaria in different sites of the INDIA. Alongside, with the help of next-generation genomics study, the team has studied the antimalarial drug resistance in India. Further, he has extended his research in the development of Humanized mice for the study of liver-stage malaria and identification of molecular marker(s) for the Artemisinin resistance. At present, his research focuses on understanding the role of B cells in the activation of CD8+ T cells in malaria. Received the CSIR-SRF (Senior Research Fellow) award-2018, FIMSA (Federation of Immunological Societies of Asia-Oceania) Travel Bursary award to attend the IUIS-IIS-FIMSA Immunology course-2019',institutionString:"Nirma University",institution:{name:"Nirma University",country:{name:"India"}}},{id:"334383",title:"Ph.D.",name:"Simone",middleName:"Ulrich",surname:"Ulrich Picoli",slug:"simone-ulrich-picoli",fullName:"Simone Ulrich Picoli",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/334383/images/15919_n.jpg",biography:"Graduated in Pharmacy from Universidade Luterana do Brasil (1999), Master in Agricultural and Environmental Microbiology from Federal University of Rio Grande do Sul (2002), Specialization in Clinical Microbiology from Universidade de São Paulo, USP (2007) and PhD in Sciences in Gastroenterology and Hepatology (2012). She is currently an Adjunct Professor at Feevale University in Medicine and Biomedicine courses and a permanent professor of the Academic Master\\'s Degree in Virology. She has experience in the field of Microbiology, with an emphasis on Bacteriology, working mainly on the following topics: bacteriophages, bacterial resistance, clinical microbiology and food microbiology.",institutionString:null,institution:{name:"Universidade Feevale",country:{name:"Brazil"}}},{id:"229220",title:"Dr.",name:"Amjad",middleName:"Islam",surname:"Aqib",slug:"amjad-aqib",fullName:"Amjad Aqib",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229220/images/system/229220.png",biography:"Dr. Amjad Islam Aqib obtained a DVM and MSc (Hons) from University of Agriculture Faisalabad (UAF), Pakistan, and a PhD from the University of Veterinary and Animal Sciences Lahore, Pakistan. Dr. Aqib joined the Department of Clinical Medicine and Surgery at UAF for one year as an assistant professor where he developed a research laboratory designated for pathogenic bacteria. Since 2018, he has been Assistant Professor/Officer in-charge, Department of Medicine, Manager Research Operations and Development-ORIC, and President One Health Club at Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan. He has nearly 100 publications to his credit. His research interests include epidemiological patterns and molecular analysis of antimicrobial resistance and modulation and vaccine development against animal pathogens of public health concern.",institutionString:"Cholistan University of Veterinary and Animal Sciences",institution:{name:"University of Agriculture Faisalabad",country:{name:"Pakistan"}}},{id:"333753",title:"Dr.",name:"Rais",middleName:null,surname:"Ahmed",slug:"rais-ahmed",fullName:"Rais Ahmed",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333753/images/20168_n.jpg",biography:null,institutionString:null,institution:{name:"University of Agriculture Faisalabad",country:{name:"Pakistan"}}},{id:"62900",title:"Prof.",name:"Fethi",middleName:null,surname:"Derbel",slug:"fethi-derbel",fullName:"Fethi Derbel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/62900/images/system/62900.jpeg",biography:"Professor Fethi Derbel was born in 1960 in Tunisia. He received his medical degree from the Sousse Faculty of Medicine at Sousse, University of Sousse, Tunisia. He completed his surgical residency in General Surgery at the University Hospital Farhat Hached of Sousse and was a member of the Unit of Liver Transplantation in the University of Rennes, France. He then worked in the Department of Surgery at the Sahloul University Hospital in Sousse. Professor Derbel is presently working at the Clinique les Oliviers, Sousse, Tunisia. His hospital activities are mostly concerned with laparoscopic, colorectal, pancreatic, hepatobiliary, and gastric surgery. He is also very interested in hernia surgery and performs ventral hernia repairs and inguinal hernia repairs. He has been a member of the GREPA and Tunisian Hernia Society (THS). During his residency, he managed patients suffering from diabetic foot, and he was very interested in this pathology. For this reason, he decided to coordinate a book project dealing with the diabetic foot. Professor Derbel has published many articles in journals and collaborates intensively with IntechOpen Access Publisher as an editor.",institutionString:"Clinique les Oliviers",institution:null},{id:"300144",title:"Dr.",name:"Meriem",middleName:null,surname:"Braiki",slug:"meriem-braiki",fullName:"Meriem Braiki",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/300144/images/system/300144.jpg",biography:"Dr. Meriem Braiki is a specialist in pediatric surgeon from Tunisia. She was born in 1985. She received her medical degree from the University of Medicine at Sousse, Tunisia. She achieved her surgical residency training periods in Pediatric Surgery departments at University Hospitals in Monastir, Tunis and France.\r\nShe is currently working at the Pediatric surgery department, Sidi Bouzid Hospital, Tunisia. Her hospital activities are mostly concerned with laparoscopic, parietal, urological and digestive surgery. She has published several articles in diffrent journals.",institutionString:"Sidi Bouzid Regional Hospital",institution:null},{id:"229481",title:"Dr.",name:"Erika M.",middleName:"Martins",surname:"de Carvalho",slug:"erika-m.-de-carvalho",fullName:"Erika M. de Carvalho",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229481/images/6397_n.jpg",biography:null,institutionString:null,institution:{name:"Oswaldo Cruz Foundation",country:{name:"Brazil"}}},{id:"186537",title:"Prof.",name:"Tonay",middleName:null,surname:"Inceboz",slug:"tonay-inceboz",fullName:"Tonay Inceboz",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/186537/images/system/186537.jfif",biography:"I was graduated from Ege University of Medical Faculty (Turkey) in 1988 and completed his Med. PhD degree in Medical Parasitology at the same university. I became an Associate Professor in 2008 and Professor in 2014. I am currently working as a Professor at the Department of Medical Parasitology at Dokuz Eylul University, Izmir, Turkey.\n\nI have given many lectures, presentations in different academic meetings. I have more than 60 articles in peer-reviewed journals, 18 book chapters, 1 book editorship.\n\nMy research interests are Echinococcus granulosus, Echinococcus multilocularis (diagnosis, life cycle, in vitro and in vivo cultivation), and Trichomonas vaginalis (diagnosis, PCR, and in vitro cultivation).",institutionString:"Dokuz Eylül University",institution:{name:"Dokuz Eylül University",country:{name:"Turkey"}}},{id:"71812",title:"Prof.",name:"Hanem Fathy",middleName:"Fathy",surname:"Khater",slug:"hanem-fathy-khater",fullName:"Hanem Fathy Khater",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/71812/images/1167_n.jpg",biography:"Prof. Khater is a Professor of Parasitology at Benha University, Egypt. She studied for her doctoral degree, at the Department of Entomology, College of Agriculture, Food and Natural Resources, University of Missouri, Columbia, USA. She has completed her Ph.D. degrees in Parasitology in Egypt, from where she got the award for “the best scientific Ph.D. dissertation”. She worked at the School of Biological Sciences, Bristol, England, the UK in controlling insects of medical and veterinary importance as a grant from Newton Mosharafa, the British Council. Her research is focused on searching of pesticides against mosquitoes, house flies, lice, green bottle fly, camel nasal botfly, soft and hard ticks, mites, and the diamondback moth as well as control of several parasites using safe and natural materials to avoid drug resistances and environmental contamination.",institutionString:null,institution:{name:"Banha University",country:{name:"Egypt"}}},{id:"99780",title:"Prof.",name:"Omolade",middleName:"Olayinka",surname:"Okwa",slug:"omolade-okwa",fullName:"Omolade Okwa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/99780/images/system/99780.jpg",biography:"Omolade Olayinka Okwa is presently a Professor of Parasitology at Lagos State University, Nigeria. She has a PhD in Parasitology (1997), an MSc in Cellular Parasitology (1992), and a BSc (Hons) Zoology (1990) all from the University of Ibadan, Nigeria. She teaches parasitology at the undergraduate and postgraduate levels. She was a recipient of a Commonwealth fellowship supported by British Council tenable at the Centre for Entomology and Parasitology (CAEP), Keele University, United Kingdom between 2004 and 2005. She was awarded an Honorary Visiting Research Fellow at the same university from 2005 to 2007. \nShe has been an external examiner to the Department of Veterinary Microbiology and Parasitology, University of Ibadan, MSc programme between 2010 and 2012. She is a member of the Nigerian Society of Experimental Biology (NISEB), Parasitology and Public Health Society of Nigeria (PPSN), Science Association of Nigeria (SAN), Zoological Society of Nigeria (ZSN), and is Vice Chairperson of the Organisation of Women in Science (OWSG), LASU chapter. She served as Head of Department of Zoology and Environmental Biology, Lagos State University from 2007 to 2010 and 2014 to 2016. She is a reviewer for several local and international journals such as Unilag Journal of Science, Libyan Journal of Medicine, Journal of Medicine and Medical Sciences, and Annual Research and Review in Science. \nShe has authored 45 scientific research publications in local and international journals, 8 scientific reviews, 4 books, and 3 book chapters, which includes the books “Malaria Parasites” and “Malaria” which are IntechOpen access publications.",institutionString:"Lagos State University",institution:{name:"Lagos State University",country:{name:"Nigeria"}}},{id:"273100",title:"Dr.",name:"Vijay",middleName:null,surname:"Gayam",slug:"vijay-gayam",fullName:"Vijay Gayam",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/273100/images/system/273100.jpeg",biography:"Dr. Vijay Bhaskar Reddy Gayam is currently practicing as an internist at Interfaith Medical Center in Brooklyn, New York, USA. He is also a Clinical Assistant Professor at the SUNY Downstate University Hospital and Adjunct Professor of Medicine at the American University of Antigua. He is a holder of an M.B.B.S. degree bestowed to him by Osmania Medical College and received his M.D. at Interfaith Medical Center. His career goals thus far have heavily focused on direct patient care, medical education, and clinical research. He currently serves in two leadership capacities; Assistant Program Director of Medicine at Interfaith Medical Center and as a Councilor for the American\r\nFederation for Medical Research. As a true academician and researcher, he has more than 50 papers indexed in international peer-reviewed journals. He has also presented numerous papers in multiple national and international scientific conferences. His areas of research interest include general internal medicine, gastroenterology and hepatology. He serves as an editor, editorial board member and reviewer for multiple international journals. His research on Hepatitis C has been very successful and has led to multiple research awards, including the 'Equity in Prevention and Treatment Award” from the New York Department of Health Viral Hepatitis Symposium (2018) and the 'Presidential Poster Award” awarded to him by the American College of Gastroenterology (2018). 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His research work has been published in various high-impact factor journals (Science, PNAS, Nature Medicine) with a high number of citations. He has received many awards and honors in India and abroad including various Young Scientist Awards, BBSRC India Partnering Award, and Dr. JC Bose National Award of Department of Biotechnology, Min. of Science and Technology, Govt. of India. Dr. Saxena is a fellow of various international societies/academies including the Royal College of Pathologists, United Kingdom; Royal Society of Medicine, London; Royal Society of Biology, United Kingdom; Royal Society of Chemistry, London; and Academy of Translational Medicine Professionals, Austria. He was named a Global Leader in Science by The Scientist. 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