Open access peer-reviewed chapter

Traditional Islamic Herbal Medicine and Complementary Therapies

Written By

Sahabjada Siddiqui, Afsana Khatoon, Khursheed Ahmad, Shivbrat Upadhyay, Aditi Srivastava, Anchal Trivedi, Ishrat Husain, Rumana Ahmad, Mohsin Ali Khan and Md Arshad

Submitted: 26 August 2021 Reviewed: 07 December 2021 Published: 12 January 2022

DOI: 10.5772/intechopen.101927

From the Edited Volume

Complementary Therapies

Edited by Mario Bernardo-Filho, Redha Taiar, Danúbia da Cunha de Sá-Caputo and Adérito Seixas

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Abstract

Herbal products found abundantly in several plants are the rich source of phytochemicals with a wide range of pharmacological activities and few adverse effects. Medicinal plants contain active ingredients that assist the body in reestablishing its natural balance and healing itself. Various herbs, which are commonly used in traditional Islamic medicine, can have an impact on human body systems. Natural products are primary sources of effective drugs with novel structures and distinct mechanisms of action for the treatment of various types of complications as well as the drug discovery process. The various pharmacological properties such as antimicrobial, anticancer, antioxidant, antihypertensive, immunomodulatory, anti-inflammatory and anti-diabetic properties of several natural products are well documented in the Ayurveda and Unani system of medicine. Some of the natural products’ active ingredients have been documented, but the majority are still being researched as complementary medicine. As a result, more research is required to investigate their complementary medicine system. The present chapter provides a comprehensive update on selected traditional Islamic medicinal plants and their bioactive products mentioned in Islamic scriptures as complementary therapies to various diseases. The chapter also provides an in-depth update of pharmacological and clinical studies of natural products with special emphasis on cancer and diabetes.

Keywords

  • traditional Islamic herbs
  • complementary therapies
  • herbal products
  • pharmacological properties

1. Introduction

According to the World Health Organization, an estimated 80% of people around the world use herbal medicine. Studies show that certain herbs effectively treat several health issues, like allergies, premenstrual syndrome, chronic fatigue, cancer, diabetes and many more. India is one of the big resources of medicinal plants and natural products due to its geological diversity. In recent years, various researches have been conducted on medicinal plants and spices worldwide. Plant-derived chemicals have attracted the attention of the scientific community for their various potential positive qualities. Studies have shown that polyphenols are anti-oxidants, anti-inflammatory, cardiac and neuroprotective, as well as having anti-cancer properties [1, 2]. Some of these natural chemicals have been included in clinical trials due to their inherent biological activity in a variety of disease models [3, 4], as they exhibited promising benefits in terms of boosting the anti-proliferative response and reducing the toxicity of conventional treatments.

Islamic medicine, often known as Arabic medicine in medical history, is the science of medicine developed during the Islamic Golden Age, which lasted from the ninth to thirteenth centuries. Although the main medical tradition was Greek, it was influenced by Islamic or Prophetic Medicine, as well as folk medicine to a lesser extent. The Holy Quran has provided the knowledge for a variety of crops, including grains, seeds, and fodder, as well as their germination and growth processes in several Surah. Plants are considered a gift from God, and the Quran mentions various plant names such as Date palms, figs, olives, ginger, grapes, miswak, onion, barley, garlic, pomegranates, camphor, Christ’s thorns, bottle gourds and other significant therapeutic herbs and plants utilized as food [5, 6].

Various medicinal plants and nutraceuticals derived from different natural resources, as well as their products such as polyphenolic components, flavones, flavonoids, and antioxidants, have been found to provide significant protection against a variety of diseases [7]. Epidemiological observations show that various traditional Islamic medicinal plants have powerful disease inhibiting properties [6, 8]. Currently, developing a preventive/therapeutic drug that reduces the particular disease without harming normal cells, is the primary goal of the research performed. For instance, in the case of cancer treatment, some of the methods used by the experts to cure the condition include tumor debulking, chemotherapies, radiotherapies, targeted treatments, immunotherapies, stem cell transplants, and photodynamic therapies [9]. Around the world, researchers are trying to develop new strategies to eradicate the diseases.

The present chapter summarizes the recently reported pharmacologically and therapeutically based medicinal plants and its products mentioned in Islamic scriptures. The chapter also highlights the recent studies of medicinal plants and their natural products based on in vitro and in vivo and clinical investigation.

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2. Traditional Islamic medicinal plants and their products

2.1 Dates palm (Phoenix dactylifera L.) fruits

Phoenix dactylifera L. (P. dactylifera), often known as date palm, is one of the oldest and most important crops in Arab countries and North Africa. Apart from that, dates are also cultivated around the world and in India, southern California, Arizona and Texas [10]. The date palm tree is a part of the family Arecaceae. Date palm is a multifunctional plant that contains fiber, carbohydrates, minerals, vitamins and various phytochemicals, which were used traditionally because of having great therapeutic properties [11]. Therapeutic benefits of Ajwa dates fruits are well documented in Islamic scriptures such as Hadith and other works of Islamic literature. According to Al-Bukhaari (5445) and Muslim (2047), narrated by Sa‘d ibn Abi Waqqaas that the Prophet (PBUH) said: “Whoever eats seven Ajwa dates in the morning, will not be harmed by any poison or witchcraft that day.”

Date palm fruit has been described in traditional and alternative medicine to provide several health benefits including anticholesteremic, antidiabetic, anti-inflammatory, antioxidant, hepatoprotective and anticancer effects [12]. According to prior phytochemical studies, Date pulp fruit contains about 80% reducing sugars, including fructose, glucose, galactose, and maltose, as well as flavonoids, glycosides, polyphenols, and phytosterols [13, 14]. Phytochemicals present in dates palm fruits exhibit anti-inflammatory, cardioprotective, antioxidant, hypolipidemic and anti-apoptotic properties [15]. The main bioactive components present dates palm pulp are Carotenoids (lutein and β-carotene), phytosterols and phytoestrogens (β-sitosterol, stigmasterol, campesterol, daidzein, genistein and isofucosterol), flavonoids (apigenin, luteolin, quercetin, isoquercetrin, rutin and kaempferol) and phenolic acids (benzoic acid derivatives; p-hydroxybenzoic acid, protocatechuic acid, vanillic acid, gallic acid and syringic acid, and cinnamic acid derivatives; o-coumaric acid, p-coumaric acid, caffeic acid, and ferulic acid) (Figure 1) [10, 16].

Figure 1.

Chemical structure of principal bioactive components found in date palm (Phoenix dactylifera L.) fruits.

2.1.1 Utilization of date palm fruit and its products as complementary therapies

2.1.1.1 Cancer

The ethyl acetate fraction of P. dactylifera fruit extract has shown the antifibrotic (expression of fibronectin-1 and alpha-smooth muscle actin) and antiproliferative activity in tumor necrosis factor (TNF) stimulated pancreatic cancer cells in vitro [10]. In addition, the ethyl acetate fraction of P. dactylifera has shown the anticancer effect against prostate cancer cells [17], ethyl alcohol extract against human hepatocellular carcinoma hepatoma G2 (HepG2) cells and triple-negative mammary carcinoma MDA-MB-231 cells [18, 19] and methanolic extract against human breast adenocarcinoma Michigan Cancer Foundation-7 (MCF-7) cells in vitro [20]. In a previous study, an aqueous extract of P. dactylifera has shown the anticancer potential in diethylnitrosamine-induced hepatocellular carcinoma in Wistar rats [21]. P. dactylifera has improved the treatment outcome of pediatric cancer patients clinically [22].

2.1.1.2 Diabetes

Low glycemic index (GI) diets have been proven to be effective in the treatment of diabetes. Dates can be classed as a low GI superfood because of their high fructose content, which is sweeter and less diabetogenic than glucose [23]. P. dactylifera fruit based-diets have alleviated hyperglycemia in alloxan-induced diabetic rats [24]. A previous study has revealed significant anti-hyperglycemic effects of dates fruits in diabetes management of hyperglycemic Sprague-Dawley rats [25] and diosmetin glycosides isolated from the epicarp of date fruits have significantly alleviated the biochemical profile of alloxan diabetic male rats [26].

2.1.1.3 Antibacterial and antiviral

The use of dates is also important for antimicrobial activities. The in vitro studies have demonstrated that date fruit exhibits antibacterial, antiviral, anti-inflammatory and anti-angiogenic activity [15, 27].

2.1.1.4 Hepatoprotective and antioxidant

Date palm fruit has shown the protective effect on dimethoate induced-oxidative stress in rat liver [28]. Moreover, date palm fruits have shown anti-hyperlipidemic and hepatoprotective effects in hyperlipidemia and fatty liver male albino rats [29].

2.1.1.5 Pregnancy and delivery

The use of dates is especially important for pregnant and postnatal women. Women who consume dates before and after giving birth might strengthen their uterine muscles by consuming dates [20]. Consumption of date fruit in the last 4 weeks before labor reduced the need for initiation and augmentative labor and resulted in a better delivery outcome [30]. Due to their high fiber, iron and trace element contents, as well as their high energy and low GI, date fruits seem to be the ideal superfood for today’s health-conscious age.

2.2 Fig (Ficus carica) fruit

One of the largest angiosperm genus, Ficus belonging to the family of Moraceae (Mulberry) are perennial plants comprising of over 800 different species including climbers, trailers, and epiphytes distributed around the tropical and sub-tropical regions worldwide [31, 32]. Ficus carica (F. carica), a deciduous dicotyledonous tree is the most important member of the genus commonly referred to as ‘fig’. Indigenous to Egypt (East Mediterranean region), F. carica was initially introduced to different civilizations throughout the world including England, United States (US), East and West South Central, South Atlantic and Pacific [33]. Despite, its origins in the Sub-Himalayan regions of the Bengal and Central Indian subcontinents, it has been widely cultivated all around the globe. However, some of the world’s major producers of figs for their dry and consumption were US, Turkey and Greece [33].

Bush/small tree-like appearance with single, alternating and large foliage, deep lobes with three or seven lobes; rough and hairy on the top surface; soft and hairy underneath along with smooth and gray bark. In addition to being cultivated from ancient times, they were found growing in the wild in dry and sunny places with rich and fresh soil, as well as in rocky locations. A reasonably permeable and easy draining soil is ideal for the plant’s growth; nevertheless, it can also grow in nutritionally poor soil [34]. The edible part of F. carica, the fruit is seed-bearing, fleshy, hollow, and receptacle-shaped. Figs do indeed have a long history of medicinal, mythological, and ecclesiastical applications [35, 36, 37, 38]. They are bad cholesterol-free, low in sodium and an excellent source of minerals (K, Zn, Mg, Fe, N, Ca, and P), dietary fibers, carbohydrates, sugars, vitamins (water-soluble—B1, B2, B3 and C; fat-soluble—A), good cholesterol and essential amino acids.

Figs have acquired a considerable amount of folkloric importance and still invite the attention of researchers globally for their pharmaceutical properties to be used as complementary medicine. Ayurveda, Unani, and Siddha are the classical medicine systems of Ayurveda that have acknowledged the medicinal benefits of fig [39]. Therefore, it promises to treat and cure disorders of endocrine (diabetes), ventilatory, cardiovascular, digestive (ulcers and vomiting), urinary, reproductive (menstrual discomfort), and immune systems, as well as infectious diseases of the skin, scabies, and gonorrhea [40].

Phytochemical analysis results revealed a number of secondary metabolites being isolated from different parts of F. carica which are phytosterols, anthocyanin pigments, essential amino acids, phenols (proanthocyanidins), essential fatty acids, triterpenoids, coumarins, alcohols, and other volatile counterparts [41, 42].

Linolenic acid (53.1%) was found to be the most prominent fatty acid present in dried figs followed by linoleic acid (21.1%), palmitic acid (13.8%), and oleic acid (9.8%) [41]. Phenolic compounds; 3-O- and 5-O-caffeoylquinic acids, ferulic acid, quercetin-3-O-glucoside, quercetin-3-O-rutinoside, psoralen, and bergapten isolated from the fruit pulp [43]. However, numerous volatile components namely 3-methyl-butanal, 2-methyl-butanal, (E)-2-pentanal, hexanal, heptanal, octanal, and nonanal, 1-penten-3-ol, 3-methylbutanol, benzyl alcohol, (E)-2-nonenol, and phenylethyl alcohol, ketone: 6-methyl-5-hepten-2-one, esters: methyl hexanoate, methyl salicylate, and ethyl salicylate, limonene, menthol, α-pinene, β-pinene, linalool, eucalyptol, α-cubenene, copaene, β-caryophyllene, τ-muurolene, τ-cadinene, and germacrene D and β-cyclocitral were found in the F. carica fruits (Figure 2) [44].

Figure 2.

Chemical structure of principal bioactive components found in fig (Ficus carica) fruits.

The fruits have emerged as an outstanding complementary medicine that could be used in treating leprosy, nasal hemorrhage, and deficiency disorders as well as are used in various drug preparations [45].

2.2.1 Utilization of F. carica fruits and its products as complementary therapies

2.2.1.1 Cardioprotective (hypotensive effect)

F. carica is one of the five plants mentioned in the Quran widely used in the treatment of cardiovascular diseases. Nevertheless, its hypertensive properties are not well documented. However, a study reveals that fruit extract of F. caricasignificantly reduced the level of blood pressure in normal as well as glucose-treated (hypertensive) rats. This effect has been attributed due to the presence of flavonoids, phenols and potassium ions which alter the level of glucose/fructose stimulating cardioinhibitory, antihypertensive and diuretic effects [46].

2.2.1.2 Cancer

Methanolic fruit extract of F. carica possessed antiproliferative activity against hepatocyte-derived carcinoma cells with an IC50 value >2000 μg/mL [47]. Virtual screening, molecular docking and dynamics simulation investigations were combined to give a structural insight into the putative binding mechanism of prospective drug-like phytocomponents of F. carica with crucial molecular targets which play a significant role in the pathogenesis of several cancer. β-Bourbonene was found to show the best binding with topoisomerase-I, topoisomerase-II, and Vascular Endothelial Growth Factor-2 (VEGFR-2), thereby, altering their functions to alter the pathogenesis [48].

2.2.1.3 Antioxidant and antihyperlipidemic activity

Methanolic fruit extract of F. carica revealed strong antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) dye with an IC50 value of 13.402 μg/mL [47]. The most prominent phenolic compounds: quercetin 3-O-rutinoside, dihydroxybenzoic acid di-pentoside and apigenin 8-C-glucoside were most abundantly present in the aqueous-ethanolic extract of Tunisian F. carica. Due to these phytoconstituents, improved antioxidant status and lower lipid peroxidation were observed suggesting their protective role [49].

2.2.1.4 Anti-diabetic activity

As a promising nutritional intervention for acute postprandial glucose and insulin homeostasis, F. carica fruit supplementation might also be used in the treatment of severe metabolic diseases such as hyperglycaemic condition and type 2 diabetes mellitus to optimize the glucose level in these conditions [50].

2.2.1.5 Antispasmodic and antiplatelet activities

In a previous study, it has been found that the fig seems to have a spasmolytic action that might be mediated by activation of the K+-ATP channel, which supports some of its therapeutic uses in hyperactive gastrointestinal illnesses, and its antiplatelet effect [51].

2.3 Black cumin (Nigella sativa) seed

Nigella sativa (N. sativa, family Ranunculaceae), popularly known as black seed or black cumin or Kalonji in Hindi, is an annual herb with various pharmacological properties and a widely used medicinal herb across the world with a rich historical and religious background. N. sativa is native to Southern Europe, North Africa and Southwest Asia and it is grown in many countries around the world like the Middle Eastern Mediterranean region, South Europe, India, Pakistan, Syria, Turkey, Saudi Arabia [52, 53]. Black seeds and oil have been used in traditional medicine for more than 2000 years, and Hippocrates and Discroides termed it “the Melanthion” [54]. It is an important drug in various traditional system of medicine like Unani and Tibb, Ayurveda and Siddha. Traditionally, N. sativa has been used to treat a wide range of illnesses, diseases, and conditions affecting the respiratory system, digestive tract, kidney and liver function, cardiovascular system, and immune system, as well as for overall well-being [55]. In Arabic, Nigella is known as ‘Habbatul barakah’, which means the seed of blessing. In Islam, It is considered as one of the most effective kinds of curing medicine available as it was stated in one of the Prophetic hadiths that black seed is the remedy for all illness except death. In Tibb-e-Nabwi (Prophetic Medicine), it is suggested to use it on a regular basis [56]. Black seeds have quite a rich history of folkloric use as food and medicine in Indian, Arabian, Southeast Asian, and Middle Eastern civilizations, and have traditionally been used to cure asthma, bronchitis, rheumatism, and other inflammatory illnesses. Extract prepared from black seed is used for the treatment of indigestion, diarrhea, loss of appetite, amenorrhoea, dropsy, and dysmenorrhoea and useful in the cure of skin eruptions and worms [57].

Various therapeutic attributes of black seed and its active component thymoquinone have been shown in in vitro and in vivo investigations, including anti-cancer [58], anti-microbial [58], anti-pyretic, contraceptive and anti-fertility, anti-oxytocic [52], antitussive, anti-inflammatory [59], and antioxidant properties [60]. Black seed has been shown to have anticancer action in blood, breast, colon, pancreatic, liver, lung, fibrosarcoma, prostate, and cervical cancer cell lines, as well as in animal models of lung, kidney, skin, colon, and breast cancer [61]. Phytochemical investigation of N. sativa revealed the presence of hundreds of phytoconstituents, mostly alkaloids, saponins, sterols, and essential oil.

The most important active compounds are thymoquinone (30–48%), thymohydroquinone, dithymoquinone, p-cymene (7–15%), carvacrol (6–12%), 4-terpineol (2–7%), t-anethol (1–4%), sesquiterpene longifolene (1–8%) α-pinene and thymol [62]. Among the various active components reported thus far, thymoquinone, which is a major component of essential oil, is the most bioactive chemical and has a variety of therapeutic properties (Figure 3).

Figure 3.

Chemical structure of principal bioactive components found in black cumin (Nigella sativa) seed.

2.3.1 Utilization of black seed and its products as complementary therapies

2.3.1.1 Anticancer activity

Thymoquinone, the active compound of the black seed helps to train T cells in vitro for adoptive T-cell therapy against cancer and infectious diseases. The cytotoxic effects of different Black seed extracts as an adjuvant therapy to doxorubicin on human MCF-7 breast cancer cells was reported. The lipid extract of black seed was found to be cytotoxic against MCF-7 cells, with a lethal concentration 50 (LC50) of 2.720 ± 0.232 mg/mL, while the aqueous extract was found to be cytotoxic at concentrations as high as 50 mg/mL. In vitro and in vivo studies showed the antitumor and anti-angiogenic effects of thymoquinone on osteosarcoma [63]. Thymoquinone induced a higher percentage of growth inhibition and apoptosis in the human osteosarcoma cell line sarcoma osteogenic-2 (SaOS-2) and inhibits tumor angiogenesis and tumor growth through suppressing nuclear factor kappa light chain enhancer of activated B cells (NF-κB) and its regulated molecules. Thymoquinone cytotoxicity was also studied in human cervical squamous carcinoma cells (SiHa). Thymoquinone’s anticancer effects on breast cancer cells, as well as its potential effect on the peroxisome proliferator-activated receptors (PPAR)-activation pathway, were investigated [64]. It was discovered that thymoquinone had a strong antiproliferative effect in breast cancer cells, and cytotoxicity was increased when thymoquinone was combined with doxorubicin and 5-fluorouracil. Migration and invasive properties of MDA-MB-231 cells were also reduced in the presence of thymoquinone. N. sativa volatile oil in the diet of male Wister rats for 30 weeks significantly reduced malignant and benign colon tumor sizes, incidences and multiplicities.

2.3.1.2 Antimicrobial activity

Black cumin is one of the most inspirational medicinal plants, with potent antibacterial, antifungal, antiviral, and antiparasitic properties. Thymoquinone isolated from N. sativa seeds showed a broader spectrum of antibacterial activity against gram-positive and gram-negative bacteria, including Bacillus, Listeria, Enterococcus, Micrococcus, Staphylococcus, Pseudomonas, Escherichia, Salmonella, Serovar, and Vibrio parahaemolyticus, as well as inhibiting the formation of bacterial biofilms [65]. Different extracts of black cumin and thymoquinone were found to have potent fungicidal activity against dermatophyte strains such as Trichophyton mentagrophytes and Microsporum gypseum, which was superior to fluconazole but not as potent as ketoconazole [65]. Complete recovery and retroversion of a 46-year-old HIV-positive patient were observed after therapy with 10 mL of black seed twice daily for 6 months, according to a case report done by Onifade et al. [66]. In a mouse model, N. sativa seed oil was observed to reduce viral load to undetectable levels in the liver and spleen after 10 days of intraperitoneal injection [65].

2.3.1.3 Antioxidant activity

In vivo and in vitro investigations have shown that N. sativa possesses potent antioxidant properties [67]. Collagen-induced arthritis was used to test the antioxidant and antiarthritic effects of thymoquinone in Wistar rats [52]. After two months of contemporaneous ingestion of Allium sativum and N. sativa seed, plasma malondialdehyde (MDA) levels were significantly reduced, with enhanced activity in erythrocyte glutathione peroxidase (GSH-Px) and superoxide dismutase [68].

2.3.1.4 Antidiabetic activity

The administration of black cumin seed to streptozotocin-induced diabetic rats for one month resulted in a significant decrease in fasting plasma glucose, serum MDA, interleukin-6, and immunoglobulin A, G, and M, as well as a significant increase in endogenous antioxidant enzymes such as SOD, Glutathione-S-transferase, and catalase expression. Diabetes-induced elevations in tissue MDA and blood glucose were greatly reduced in rats treated with N. sativa extract and oil, as well as thymoquinone, and serum insulin and tissue SOD were dramatically enhanced. N. sativa and thymoquinone have been shown to be effective in the treatment of diabetics and the preservation of -cells from oxidative stress [69]. A placebo was given to 99 diabetic patients in an experimental randomized controlled study, while two treatment groups received oral black seed oil. Black seed oil at 1.5 and 3 mL/day for 20 days resulted in significant reductions in glycated hemoglobin A1c and random blood sugar levels [70].

2.3.1.5 Antihypertensive activity

According to a nonrandomized controlled trial, 57 patients who were given 2 g daily supplements of black cumin for one year showed a significant reduction in systolic, diastolic, and mean arterial BP, heart rate, TC, LDL-c, the fractions of TC/HDL-c, and LDL-c/HDL-c, while serum HDL-c was suggestively raised when compared to baseline values and the control group. It was also used to assess the blood pressure-lowering capability and possible processes of N. sativa in a rat model, and it was discovered that the seed oil and nicardipine-treated groups had significantly lower blood pressure [71].

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3. Conclusions

Medicinal plants are great sources of phytochemicals, which are abundant in a variety of plants and have few negative effects. They include active chemicals that help the body recover itself and re-establish its natural equilibrium. Traditional Islamic natural products are important sources of therapeutic medications with innovative structures and modes of action for the treatment of a variety of ailments as well as the drug discovery process. The recently reported pharmacologically and therapeutically based medicinal plants and their products that are mentioned in Islamic scriptures are presented in this chapter. The current study also emphasizes recent in vitro, in vivo, and clinical investigations of medicinal plants and their natural compounds. According to these reports, dates palm fruits, figs, and black seeds can be used for a variety of therapeutic applications, and these plant products may hold substantial promise for the development of novel therapeutic strategies for a variety of human diseases.

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Acknowledgments

This work was supported by Cell and Tissue Culture Lab, Department of Biotechnology and Department of Biochemistry, Era University, Lucknow, India.

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Conflict of interest

The authors declare no conflict of interest.

References

  1. 1. Del Rio D, Rodriguez-Mateos A, Spencer JP, Tognolini M, Borges G, Crozier A. Dietary (poly) phenolics in human health: Structures, bioavailability, and evidence of protective effects against chronic diseases. Antioxidants & Redox Signaling. 2013;18(14):1818-1892. DOI: 10.1089/ars.2012.4581
  2. 2. Milanizadeh S, Reza Bigdeli M. Pro-apoptotic and anti-angiogenesis effects of olive leaf extract on spontaneous mouse mammary tumor model by balancing vascular endothelial growth factor and endostatin levels. Nutrition and Cancer. 2019;71(8):1374-1381. DOI: 10.1080/01635581.2019.1609054
  3. 3. Butler MS, Robertson AA, Cooper MA. Natural product and natural product derived drugs in clinical trials. Natural Product Reports. 2014;31(11):1612-1661. DOI: 10.1039/C4NP00064A
  4. 4. Seca AM, Pinto DC. Plant secondary metabolites as anticancer agents: Successes in clinical trials and therapeutic application. International Journal of Molecular Sciences. 2018;19(1):263. DOI: 10.3390/ijms19010263
  5. 5. Mehmood A, Khan S, Khan S, Ahmed S, Ali A, Xue M, et al. In silico analysis of quranic and prophetic medicinals plants for the treatment of infectious viral diseases including corona virus. Saudi Journal of Biological Science. 2021;28(5):3137-3151. DOI: 10.1016/j.sjbs.2021.02.058
  6. 6. El-Seedi HR, Khalifa SA, Yosri N, Khatib A, Chen L, Saeed A, et al. Plants mentioned in the Islamic Scriptures (Holy Qur'ân and Ahadith): Traditional uses and medicinal importance in contemporary times. Journal of Ethnopharmacology. 2019;243:112007. DOI: 10.1016/j.jep.2019.112007
  7. 7. Tungmunnithum D, Thongboonyou A, Pholboon A, Yangsabai A. Flavonoids and other phenolic compounds from medicinal plants for pharmaceutical and medical aspects: An overview. Medicine. 2018;5(3):93. DOI: 10.3390/medicines5030093
  8. 8. Sofowora A, Ogunbodede E, Onayade A. The role and place of medicinal plants in the strategies for disease prevention. African Journal of Traditional, Complementary and Alternative Medicines. 2013;10(5):210-229. DOI: 10.4314/ajtcam.v10i5.2
  9. 9. Baykara O. Current therapies and latest developments in cancer treatment. Horizons in Cancer Research. 2015;57:105-156
  10. 10. Al-Alawi RA, Al-Mashiqri JH, Al-Nadabi JS, Al-Shihi BI, Baqi Y. Date palm tree (Phoenix dactylifera L.): Natural products and therapeutic options. Frontiers in Plant Science. 2017;8:845. DOI: 10.3389/fpls.2017.00845
  11. 11. Alharbi KL, Raman J, Shin HJ. Date fruit and seed in nutricosmetics. Cosmetics. 2021;8(3):59. DOI: 0.3390/cosmetics8030059
  12. 12. Hussain Mallhi T, Qadir MI, Ali M, Ahmad B, Khan YH. Ajwa date (Phoenix dactylifera): An emerging plant in pharmacological research. Pakistan Journal of Pharmaceutical Sciences. 2014;27(3):607-616
  13. 13. Al-Farsi MA, Lee CY. Nutritional and functional properties of dates: A review. Critical Reviews in Food Science and Nutrition. 2008;48(10):877-887. DOI: 10.1080/10408390701724264
  14. 14. Nasir MU, Hussain S, Jabbar S, Rashid F, Khalid N, Mehmood A. A review on the nutritional content, functional properties and medicinal potential of dates. Science Letters. 2015;3(1):17-22
  15. 15. Taleb H, Maddocks SE, Morris RK, Kanekanian AD. Chemical characterisation and the anti-inflammatory, anti-angiogenic and antibacterial properties of date fruit (Phoenix dactylifera L.). Journal of Ethnopharmacology. 2016;194:457-468. DOI: 10.1016/j.jep.2016.10.032
  16. 16. Martín-Sánchez AM, Cherif S, Ben-Abda J, Barber-Vallés X, Pérez-Álvarez JÁ, Sayas-Barberá E. Phytochemicals in date co-products and their antioxidant activity. Food Chemistry. 2014;158:513-520. DOI: 10.1016/j.foodchem.2014.02.172
  17. 17. Mirza MB, Elkady AI, Al-Attar AM, Syed FQ, Mohammed FA, Hakeem KR. Induction of apoptosis and cell cycle arrest by ethyl acetate fraction of Phoenix dactylifera L.(Ajwa dates) in prostate cancer cells. Journal of Ethnopharmacology. 2018;218:35-44. DOI: 10.1016/j.jep.2018.02.030
  18. 18. Siddiqui S, Ahmad R, Khan MA, Upadhyay S, Husain I, Srivastava AN. Cytostatic and anti-tumor potential of Ajwa date pulp against human hepatocellular carcinoma HepG2 cells. Scientific Reports. 2019;9(1):1-2. DOI: 10.1038/s41598-018-36475-0
  19. 19. Khan MA, Siddiqui S, Ahmad I, Singh R, Mishra DP, Srivastava AN, et al. Phytochemicals from Ajwa dates pulp extract induce apoptosis in human triple-negative breast cancer by inhibiting AKT/mTOR pathway and modulating Bcl-2 family proteins. Scientific Reports. 2021;11(1):10322. DOI: 10.1038/s41598-021-89420-z
  20. 20. Khan F, Ahmed F, Pushparaj PN, Abuzenadah A, Kumosani T, Barbour E, et al. Ajwa date (Phoenix dactylifera L.) extract inhibits human breast adenocarcinoma (MCF7) cells in vitro by inducing apoptosis and cell cycle arrest. PloS One. 2016;11(7):e0158963. DOI: 10.1371/journal.pone.0158963
  21. 21. Khan F, Khan TJ, Kalamegam G, Pushparaj PN, Chaudhary A, Abuzenadah A, et al. Anti-cancer effects of Ajwa dates (Phoenix dactylifera L.) in diethylnitrosamine induced hepatocellular carcinoma in Wistar rats. BMC Complementary and Alternative Medicine. 2017;17(1):1-0. DOI: 10.1186/s12906-017-1926-6
  22. 22. Al Jaouni SK, Hussein A, Alghamdi N, Qari M, El Hossary D, Almuhayawi MS, et al. Effects of Phoenix dactylifera Ajwa on infection, hospitalization, and survival among pediatric cancer patients in a university hospital: A nonrandomized controlled trial. Integrative Cancer Therapies. 2019;18:1534735419828834. DOI: 10.1177/1534735419828834
  23. 23. Miller CJ, Dunn EV, Hashim IB. The glycaemic index of dates and date/yoghurt mixed meals. Are dates ‘the candy that grows on trees’? European Journal of Clinical Nutrition. 2003;57(3):427-430. DOI: 10.1038/sj.ejcn.1601565
  24. 24. Ajiboye BO, Oloyede HO, Salawu MO. Phoenix dactylifera Linn fruit based-diets palliate hyperglycemia in alloxan-induced diabetic rats. Journal of Basic and Clinical Physiology and Pharmacology. 2020. DOI: 10.1515/jbcpp-2019-0185. Epub ahead of print. PMID: 32678802
  25. 25. Ahmed S, Alam Khan R, Jamil S. Anti hyperlipidemic and hepatoprotective effects of native date fruit variety “Aseel” (Phoenix dactylifera). Pakistan Journal of Pharmaceutical Sciences. 2016;29(6):1945-1950
  26. 26. Michael HN, Salib JY, Eskander EF. Bioactivity of diosmetin glycosides isolated from the epicarp of date fruits, Phoenix dactylifera, on the biochemical profile of alloxan diabetic male rats. Phytotherapy Research. 2013;27(5):699-704. DOI: 10.1002/ptr.4777
  27. 27. Al-Shwyeh HA. Date palm (Phoenix dactylifera L.) fruit as potential antioxidant and antimicrobial agents. Journal of Pharmacy & Bioallied Sciences. 2019;11(1):1. DOI: 10.4103/jpbs.JPBS_168_18
  28. 28. Saafi EB, Louedi M, Elfeki A, Zakhama A, Najjar MF, Hammami M, et al. Protective effect of date palm fruit extract (Phoenix dactylifera L.) on dimethoate induced-oxidative stress in rat liver. Experimental and Toxicologic Pathology. 2011;63(5):433-441. DOI: 10.1016/j.etp.2010.03.002
  29. 29. Ahmed S, Khan RA, Jamil S, Afroz S. Antidiabetic effects of native date fruit Aseel (Phoenix dactylifera L.) in normal and hyperglycemic rats. Pakistan Journal of Pharmaceutical Sciences. 2017;30(5):1797-1802
  30. 30. El-Mougy SA, Abdel-Aziz SA, Al-Shanawany M, Omar A. The gonadotropic activity of Palmae in mature male rats. Alexandria Journal of Pharmaceutical Sciences. 1991;5:156-159
  31. 31. Singh D, Singh B, Goel RK. Traditional uses, phytochemistry and pharmacology of Ficus religiosa: A review. Journal of Ethnopharmacology. 2011;134(3):565-583. DOI: 10.1016/j.jep.2011.01.046
  32. 32. Frodin DG. History and concepts of big plant genera. Taxon. 2004;53(3):753-776. DOI: 10.2307/4135449
  33. 33. Vinson JA. The functional food properties of figs. Cereal Foods World. 1999;44(2):82-87. DOI: 10.1016/B978-0-12-407849-9.00056-7
  34. 34. Barolo MI, Mostacero NR, López SN. Ficus carica L. (Moraceae): An ancient source of food and health. Food Chemistry. 2014;164:119-127. DOI: 10.1016/j.foodchem.2014.04.112
  35. 35. Jellin JM, Gregory P, Batz F, Hichens K. Pharmacist’s Letter/ Prescriber’s Letter Natural Medicines Comprehensive Database, 3rd Edition. Stockton, CA: Therapeutic Research Faculty, 2000. 1530 pp
  36. 36. Buchman DD. Herbal Medicine. New York, NY: Wings Books; 1996
  37. 37. Duke JA. The Green Pharmacy. New York, NY: Rodale Inc; 1997. p. 453
  38. 38. Goor A. The history of the fig in the Holy Land from ancient times to the present day. Economic Botany. 1965;19(2):124-135. DOI: 10.1007/BF02862824
  39. 39. Prasad PV, Subhaktha PK, Narayana A, Rao MM. Medico-historical study of “aśvattha” (sacred fig tree). Bulletin of the Indian Institute of History of Medicine (Hyderabad). 2006;36(1):1-20
  40. 40. Badgujar SB, Patel VV, Bandivdekar AH, Mahajan RT. Traditional uses, phytochemistry and pharmacology of Ficus carica: A review. Pharmaceutical Biology. 2014;52(11):1487-1503. DOI: 10.3109/13880209.2014.892515
  41. 41. Jeong WS, Lachance PA. Phytosterols and fatty acids in fig (Ficus carica, var. Mission) fruit and tree components. Journal of Food Science. 2001;66(2):278-281. DOI: 10.1111/j.1365-2621.2001.tb11332.x
  42. 42. Veberic R, Jakopic J, Stampar F. Internal fruit quality of figs (Ficus carica L.) in the Northern Mediterranean Region. Italian Journal of Food Science. 2008;20(2):255-262
  43. 43. Gibernau M, Buser HR, Frey JE, Hossaert-McKey M. Volatile compounds from extracts of figs of Ficus carica. Phytochemistry. 1997;46(2):241-244. DOI: 10.1016/S0031-9422(97)00292-6
  44. 44. Oliveira AP, Silva LR, de Pinho PG, Gil-Izquierdo A, Valentão P, Silva BM, et al. Volatile profiling of Ficus carica varieties by HS-SPME and GC–IT-MS. Food Chemistry. 2010;123(2):548-557. DOI: 10.1016/j.foodchem.2010.04.064
  45. 45. Yancheva SD, Golubowicz S, Yablowicz Z, Perl A, Flaishman MA. Efficient Agrobacterium-mediated transformation and recovery of transgenic fig (Ficus carica L.) plants. Plant Science. 2005;168(6):1433-1441. DOI: 10.1016/j.plantsci.2004.12.007
  46. 46. Alamgeer IS, Asif H, Saleem M. Evaluation of antihypertensive potential of Ficus carica fruit. Pharmaceutical Biology. 2017;55(1):1047-1053. DOI: 10.1080/13880209.2017.1278611
  47. 47. Purnamasari R, Winarni D, Permanasari AA, Agustina E, Hayaza S, Darmanto W. Anticancer activity of methanol extract of Ficus carica leaves and fruits against proliferation, apoptosis, and necrosis in Huh7it cells. Cancer Informatics. 2019;18:1176935119842576. DOI: 10.1177/1176935119842576
  48. 48. Gurung AB, Ali MA, Lee J, Farah MA, Al-Anazi KM. Molecular docking and dynamics simulation study of bioactive compounds from Ficus carica L. with important anticancer drug targets. Plos One. 2021;16(7):e0254035. DOI: 10.1371/journal.pone.0254035
  49. 49. Belguith-Hadriche O, Ammar S, del Mar CM, Turki M, Segura-Carretero A, El Feki A, et al. Antihyperlipidemic and antioxidant activities of edible Tunisian Ficus carica L. fruits in high fat diet-induced hyperlipidemic rats. Plant Foods for Human Nutrition. 2016;71(2):183-189. DOI: 10.1007/s11130-016-0541-x
  50. 50. Atkinson FS, Villar A, Mulà A, Zangara A, Risco E, Smidt CR, et al. Abscisic acid standardized fig (Ficus carica) extracts ameliorate postprandial glycemic and insulinemic responses in healthy adults. Nutrients. 2019;11(8):1757. DOI: 10.3390/nu11081757
  51. 51. Gilani AH, Mehmood MH, Janbaz KH, Khan AU, Saeed SA. Ethnopharmacological studies on antispasmodic and antiplatelet activities of Ficus carica. Journal of Ethnopharmacology. 2008;119(1):1-5. DOI: 10.1016/j.jep.2008.05.040
  52. 52. Ahmad A, Husain A, Mujeeb M, Khan SA, Najmi AK, Siddique NA, et al. A review on therapeutic potential of Nigella sativa: A miracle herb. Asian Pacific Journal of Tropical Biomedicine. 2013;3(5):337-352
  53. 53. Tavakkoli A, Mahdian V, Razavi BM, Hosseinzadeh H. Review on clinical trials of black seed (Nigella sativa) and its active constituent, thymoquinone. Journal of Pharmacopuncture. 2017;20(3):179. DOI: 10.3831/KPI.2017.20.021
  54. 54. Darakhshan S, Pour AB, Colagar AH, Sisakhtnezhad S. Thymoquinone and its therapeutic potentials. Pharmacological Research. 2015;95:138-158. DOI: 10.1016/j.phrs.2015.03.011
  55. 55. Goreja WG. Black Seed: Nature’s Miracle Remedy. New York: Amazing Herbs Press; 2003
  56. 56. Abdel-Zaher AO, Abdel-Rahman MS, ELwasei FM. Protective effect of Nigella sativa oil against tramadol-induced tolerance and dependence in mice: Role of nitric oxide and oxidative stress. Neurotoxicology. 2011;32(6):725-733. DOI: 10.1016/j.neuro.2011.08.001
  57. 57. Yarnell E, Abascal K. Nigella sativa: Holy herb of the middle East. Alternative and Complementary Therapies. 2011;17(2):99-105. DOI: 10.1089/act.2011.17203
  58. 58. Hammad Shafiq AA, Masud T, Kaleem M. Cardio-protective and anti-cancer therapeutic potential of Nigella sativa. Iranian Journal of Basic Medical Sciences. 2014;17(12):967
  59. 59. Amin B, Hosseinzadeh H. Black cumin (Nigella sativa) and its active constituent, thymoquinone: An overview on the analgesic and anti-inflammatory effects. Planta Medica. 2016;82(01/02):8-16. DOI: 10.1055/s-0035-1557838
  60. 60. Hosseinzadeh H, Taiari S, Nassiri-Asl M. Effect of thymoquinone, a constituent of Nigella sativa L., on ischemia–reperfusion in rat skeletal muscle. Naunyn-Schmiedeberg’s Archives of Pharmacology. 2012;385(5):503-508. DOI: 10.1007/s00210-012-0726-2
  61. 61. Khan A, Chen HC, Tania M, Zhang DZ. Anticancer activities of Nigella sativa (black cumin). African Journal of Traditional, Complementary and Alternative Medicines. 2011;8(5S):226-232. DOI: 10.4314/ajtcam.v8i5S.10
  62. 62. Atta-UR-Rahman AU, Malik S, Hasan SS, Choudhary MI, Ni CZ, Clardy J. Nigellidine—A new indazole alkaloid from the seeds of Nigella sativa. ChemInform. 1995;26(30):1993-1996. DOI: 10.1016/0040-4039(95)00210-4
  63. 63. Mahmoud SS, Torchilin VP. Hormetic/cytotoxic effects of Nigella sativa seed alcoholic and aqueous extracts on MCF-7 breast cancer cells alone or in combination with doxorubicin. Cell Biochemistry and Biophysics. 2013;66(3):451-460. DOI: 10.1007/s12013-012-9493-4
  64. 64. Peng L, Liu A, Shen Y, Xu HZ, Yang SZ, Ying XZ, et al. Antitumor and anti-angiogenesis effects of thymoquinone on osteosarcoma through the NF-κB pathway. Oncology Reports. 2013;29(2):571-578. DOI: 10.3892/or.2012.2165
  65. 65. Yimer EM, Tuem KB, Karim A, Ur-Rehman N, Anwar F. Nigella sativa L. (black cumin): A promising natural remedy for wide range of illnesses. Evidence-Based Complementary and Alternative Medicine. 2019;2019:1528635. DOI: 10.1155/2019/1528635. PMID: 31214267
  66. 66. Onifade AA, Jewell AP, Adedeji WA. Nigella sativa concoction induced sustained seroreversion in HIV patient. African Journal of Traditional, Complementary and Alternative Medicines. 2013;10(5):332-335
  67. 67. Ozdemir N, Kantekin-Erdogan MN, Tat T, Tekin A. Effect of black cumin oil on the oxidative stability and sensory characteristics of mayonnaise. Journal of Food Science and Technology. 2018;55(4):1562-1568. DOI: 10.1007/s13197-018-3075-4
  68. 68. Mostafa RM, Moustafa YM, Mirghani Z, AlKusayer GM, Moustafa KM. Antioxidant effect of garlic (Allium sativum) and black seeds (Nigella sativa) in healthy postmenopausal women. SAGE Open Medicine. 2013;1:2050312113517501. DOI: 10.1177/2050312113517501
  69. 69. Abdelmeguid NE, Fakhoury R, Kamal SM, Al Wafai RJ. Effects of Nigella sativa and thymoquinone on biochemical and subcellular changes in pancreatic β-cells of streptozotocin-induced diabetic rats. Journal of Diabetes. 2010;2(4):256-266. DOI: 10.1111/j.1753-0407.2010.00091.x
  70. 70. Rachman PN, Darmawan E. The efficacy of black cumin seed (Nigella sativa) oil and hypoglycemic drug combination to reduce HbA1c level in patients with metabolic syndrome risk. In: IOP Conference Series: Materials Science and Engineering. Vol. 259(1). Yogyakarta, Indonesia: IOP Publishing; 2017. p. 012018. DOI: 10.1088/1757-899X/259/1/012018
  71. 71. Badar A, Kaatabi H, Bamosa A, Al-Elq A, Abou-Hozaifa B, Lebda F, et al. Effect of Nigella sativa supplementation over a one-year period on lipid levels, blood pressure and heart rate in type-2 diabetic patients receiving oral hypoglycemic agents: Nonrandomized clinical trial. Annals of Saudi Medicine. 2017;37(1):56-63. DOI: 10.5144/0256-4947.2017.56

Written By

Sahabjada Siddiqui, Afsana Khatoon, Khursheed Ahmad, Shivbrat Upadhyay, Aditi Srivastava, Anchal Trivedi, Ishrat Husain, Rumana Ahmad, Mohsin Ali Khan and Md Arshad

Submitted: 26 August 2021 Reviewed: 07 December 2021 Published: 12 January 2022