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Chemistry and pharmacology of withania somnifera: An update
Chemistry and pharmacology of withania somnifera: An update
TANG. 2015. Feb, 5(1): 1-1
Copyright © 2015, Association of Humanitas Medicine
This is an open access article under the CC BY-NC license. (http://creativecommons.org/licenses/by-nc/3.0/)
  • Received : October 05, 2014
  • Accepted : February 24, 2015
  • Published : February 28, 2015
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About the Authors
Vikas Kumar
Neuropharmacology Research Laboratory, Department of Pharmaceutics, Indian Institute of Technology (Banaras Hindu University), Varanasi-221005, India;
vikas.phe@iitbhu.ac.in
Amitabha Dey
Neuropharmacology Research Laboratory, Department of Pharmaceutics, Indian Institute of Technology (Banaras Hindu University), Varanasi-221005, India;
Mallinath B. Hadimani
Department of Chemistry, Graduate School of Arts and Sciences, Wake Forest University, Winston-Salem, North Carolina 27106, USA;
Tatjana Marcović
Institute of Medicinal Plant Research “Dr Josif Pančić” Belgrade, Tadeuša Košćuška 1, 11000 Belgrade, Republic of Serbia;
Mila Emeraldjavascript
Phytoceuticals International, Oxford Street East, London, Ontario, N5Y 1A0, Canada

Abstract
Withania somnifera (Ashwagandha) is an important Rasayana herb and widely considered as Indian ginseng in Ayurveda. In traditional system of Indian medicine, it is used as tonic to rejuvenate the body and increase longevity. In Ayurvedic preparations, various parts of the plant have been used to treat variety of ailments that affect the human health. However, dried roots of the plant are widely used for the treatment of nervous and sexual disorders. The major active chemical constituents of this plant are withanolides, which is responsible for its wide range of biological activities. Since the beginning of the 20 th century, a significant amount of research has been done and efforts are ongoing to further explore other bioactive constituents, and many pharmacological studies have been carried out to describe their disease preventing mechanisms. In this chapter, we have reviewed the chemistry and pharmacological basis of W. somnifera in various human ailments.
Keywords
INTRODUCTION
Withania somnifera (L.) Dunal ( W. somnifera ; Solanaceae), popularly known as 'Ashwagandha' in Sanskrit and as 'Indian ginseng', in Ayurveda ( Kulkarni and Dhir, 2008 ; Puri, 2003 ). It is a green woody shrub of 200-800 cm height, found throughout the drier parts of South East Asia including India, Bangladesh, Sri-Lanka, Nepal and Pakistan, and different other parts of Australia, Africa and America ( Hepper, 1991 ; Ilayperuma et al., 2002 ; Mabberley, 2008 ; Mirjalili et al., 2009 ). In India, it is widely distributed in the provinces of Madhya Pradesh, Uttar Pradesh, Punjab Gujarat and Rajasthan ( Kulkarni and Dhir, 2008 ). It is an important Rasayana herb used in the traditional system of medicine, for more than 2500years ( Bhattacharya and Muruganandam, 2003 ). In Ayurvedic preparations, various parts of the plant have been used to treat variety of ailments ( Kulkarni and Dhir, 2008 ), however roots of the plant is used to prepare tonic which promote longevity, revitalizing the body, arresting the aging process and augmenting defense against infectious diseases ( Bhattacharya and Muruganandam, 2003 ; Singh et al., 2008 ). W. somnifera also participate as an important ingredient in many Ayurvedic formulations, which are currently commercialized in India and other countries. Ayurvedic formulations containing W. somnifera prescribed as analgesic for a variety of musculoskeletal disorders (arthritis and rheumatism), certain forms of hypertension, for stimulating sexual impulses and increases sperm counts, in gynecological practice for vaginitis and during pregnancy for breast development ( Mishra and Singh, 2005 ; Puri, 2003 ). Since ancient times W. somnifera has been considered for persons of both sexes, of all ages and at all stages of their lives as nerve tonic, aphrodisiac, adaptogen, antirheumatic agent, astringent and memory enhancer ( Bhattacharya and Muruganandam, 2003 ; Puri, 2003 ). Many pharmacological studies have been carried out to describe multiple biological properties of W. somnifera and outcomes obtained from these studies indicate that it is also useful to treat bronchitis, asthma, ulcer, cancer, emaciation, insomnia, and senile dementia ( Kulkarni and Dhir, 2008 ; Mishra and Singh, 2005 ). W. somnifera also having other multipurpose medicinal uses which are supported by different preclinical and clinical trials includes for antidiabetic, immunomodulatory, hemopoietic, neurological inflammatory disorders and Parkinson’s disease, additionally it is also useful as antioxidant, abortifacient, antibiotic, aphrodisiac, deobstruent, diuretic and sedative ( Bone, 1996 ; Kulkarni and Dhir, 2008 ; Mishra and Singh, 2005 ). Its chemopreventive properties make it a potentially useful adjunct for patients receiving radiation and chemotherapy ( Devi et al., 1992 ).
The major biochemical constituents of W. somnifera are withanolides (steroidal lactones with ergostane skeleton). The withanolides have C28 steroidal nucleus with C9 side chain, having a six membered lactone ring. Withanolides are highly oxygenated phytochemicals, and the oxidation at various sites of skeleton is responsible for the structural variations in different classes of withanolides ( Choudhary et al., 2013 ; Kulkarni and Dhir, 2008 ). In addition, different classes of withanosides, glycowithanolides, sitoindosides, alkaloids, saponins, amino acids, phenolic compounds, flavonoids and many other secondary bioactive metabolites of the plant with broad-spectrum therapeutic activity were isolated and characterized ( Elsakka et al., 1990 ; Mishra and Singh, 2005 ). Much of ashwaganda’s pharmacological activity has been attributed to two main constituents such as withaferin-A and withanolide-D ( Mirjalili et al., 2009 ).
Extensive toxicological studies and the data obtained from various clinical research works on W. somnifera was demonstrated that the plant is nontoxic in wide range of practical doses and it can be assumed that the doses in which its preparations are indicated in humans are expected to be very safe. As of today, no herb-herb or herb–drug interactions has been reported in the literature with W. somnifera ( Kulkarni and Dhir, 2008 ; Prabu et al., 2013 ; Sharada et al., 1993 ). The side effects and the long-term safety of W. somnifera are still under construction. However, large doses of W. somnifera might cause stomach upset, diarrhea, and vomiting. Based on limited human research it was reported that W. somnifera may cause sedation, possible life-threatening respiratory depression, decrease blood pressure and cause abnormal heart rhythms ( Gardner and McGuffin, 2013 ; Puri, 2003 ).
Information now available on chemistry and pharmacology of diverse types of W. somnifera extracts obtained from different parts of the plant have been reviewed which strongly suggest that appropriate combinations with other plants could be used for prevention and cure of diverse disorders and chronic diseases. In this chapter, we mainly focus on earlier and recent advancements on chemistry and pharmacological aspects of W. somnifera .
- Chemistry
The major chemical constituents of W. somnifera are withanolides, a group of naturally occurring C28 steroidal lactones with ergostane-based skeleton. Withanolides are highly oxygenated phytoconstituents, and the oxidation at various sites of skeleton is responsible for the structural variations in different classes of withanolides. Withanolides possess a wide range of biological activities ( Choudhary et al., 2013 ). Lavie and coworkers in 1965 were the first to isolate withaferin-A from W. somnifera ( Lavie et al., 1965 ). Even though several reports were published in the recent literature from various research groups about evaluating different pharmacological activities of W. somnifera , very few groups have reported synthetic analogs or semi-synthetic derivatives of its potential alkaloids. Most of the analogs synthesized are the derivatives of its chief constituent withaferin-A. Here we will briefly review some of the most important developments in recent years involving chemical modification of Withanolides.
Gunatilaka group reported the synthesis and cytotoxic profile of various derivatives of withaferin-A ( Wijeratne et al., 2014 ). They synthesized a total of 36 analogs by a variety of chemistry and compared their cytotoxicity to cytoprotective heat-shock-inducing activity to that produced by withaferin-A. By analyzing structure activity relationship for this structurally diverse group of compounds, they have found that ring aenone of withaferin-A is essential for its bioactivity. Acetylation of hydroxyl group at the 27 th position leads to the loss of potency. Their detailed studies demonstrate that the basic withanolide skeleton can be modified to selectively enhance heat shocking inducing activity ( Figs. 1 and 2 ).
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Withanolides and their Derivatives (1-26) Reported by Gunatilaka Group.
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Withanolide Derivatives Prepared by Chemical and Microbiological Transformations (27-38).
Namboothiri group has reported the total synthesis of three pyrazole containing withasomnine based alkaloids ( Varma et al., 2013 ). Starting with 4-nitro-1-butanol and commercially available aldehydes, they synthesized these molecules in overall five steps. A wide variety of methods has been reported in the earlier literature but these methods involve complex chemistry and lower yields. The work of Namboothiri group is more efficient in terms of its reaction conditions, yields and availability of starting chemicals. The key step in these syntheses is a 1,3-dipolar cycloaddition of α-bromopropyl nitroalkenes with commercially available TMSCHN 2 ( Fig. 3 ).
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Synthesis of Withasomnine Derivatives (40) by 1,3-Dipolar Cycloaddition Reaction.
With this novel method, they were able to accomplish the total synthesis of three withasomnine natural products (39 and 40a-b), and three other non-natural analogs (40c-f) ( Fig. 4 ).
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Withasomnine (39) and its Derivatives (40a-f).
Aubé and coworkers reported a series of semisynthetic analogs of withalongolide-A, which is a C-19 hydroxylated analog of withaferin-A ( Motiwala et al., 2013 ). These semisynthetic derivatives are found to be more cytotoxic than the parent molecule against a variety of cell lines ( Fig. 5 ).
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Withaferin-A (41) and Withalongolide-A (42).
A series of aliphatic esters (43a-e) were synthesized by slight modification of standard acylation procedure with acetic anhydride. These researchers were able to isolate both mono and diacetate derivatives from one-pot reactions ( Fig. 6 ).
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Acetylated Derivatives of Withalongolide-A (43a-e).
In a second set of compounds they developed benzoyl esters (44a-d) by reaction of withalongolide-A with p -chlorobenzoylchloride ( Fig. 7 ). Another interesting molecule developed was a steroidal macrocycle, compound (45). This 14-membered macrocycle with E -configuration was obtained by bis-acylation of withalongolide-A monoacetate with 4-pentenoic anhydride followed by ring closing metathesis using Grubb’s II catalyst ( Fig. 8 ).
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Benzoylated Derivatives of Withalongolide-A (44a-d).
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Macrocycle Derivative of Withalongolide-A (45).
All these synthesize d molecules were tested for cytotoxic properties against four different cell lines. Some of these semi synthetic derivatives are found to be more potent than the parent natural molecules.
Recently Darokar group developed a series of derivatives with specific modifications at carbons 5, 6 and 7 of ring B ( Joshi et al., 2014 ). In addition, they selectively converted the epoxide group to a thiirane, an amino alcohol and alcohol group, and all these derivatives were evaluated against four different cancer cell lines ( Fig. 9 ).
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Withanolide Derivatives Prepared by Aminolysis of Epoxides (46 a-h).
These researchers have successfully demonstrated that a wide variety of chemistry can be applied to withanolides, and these chemical modifications have led to a decrease in cytotoxic potency.
The reports presented here firmly establish the robust nature of withaferin-A, that can be modified chemically leading to a wide variety of biologically active novel molecules. These various structural analogs of withanolides help us understand structure-activity relationships among these varied structures. Whether these novel molecules will hold any potential for the treatment of diseases other than cancer, need to be studied.
- Pharmacology
- Anticancer activity
Numerous studies published over the last two decades indicate that W. somnifera has unique characteristics to suppress various types of cancer and it has been used as Ayurvedic remedy for the treatment of various types of cancer over two thousand years. Ashwagandha possesses anticancer properties against prostate, colon, lung, breast, leukemia, pancreatic, renal, head and neck cancer cells of humans ( Nema et al., 2013 ; Patel et al., 2013 ; Singh et al., 2011 ; Yadav et al., 2010 ), forestomach and skin cancer cells in mice ( Padmavathi et al., 2005 ). Recently the anticancerous potential of W. somnifera and its bioactive withanolides has been extensively studied by several research groups all around the world, which have discovered diverse mechanisms such as cytotoxicity, cell differentiation induction, cancer chemoprevention, cyclooxygenase-2 (COX-2) inhibition and a potential to inhibit the enzyme quinine reductase. These withanolides are highly oxygenated natural bioactive constituents which are responsible for ashwagandha’s biological properties including antitumor activity ( Mulabagal et al., 2009 ; Patel et al., 2013 ).
Withaferin-A, is a potent inhibitor of angiogenesis and thus protective in certain types of cancers ( Patel et al., 2013 ). Recent investigation identifies that W. somnifera enriched withaferin-A induces apoptosis through mechanisms ( Fig. 10 ) such as, inhibiting the activation of nuclear factor kappa-B (NF-κB) by preventing the TNF-induced activation of IκB kinase β via a thioalkylation sensitive redox mechanism ( Oh and Kwon, 2009 ), activation of tumor suppressor proteins such as p53 and pRB ( Wadhwa et al., 2013 ). It increases reactive oxygen species (ROS) generation, Par-4 induction and p38 MAP kinase activation to induce programmed cell death ( Patel et al., 2013 ). It also inhibits the Notch signaling pathway and NF-κB activation, induces Akt inactivation, death receptor 5 up-regulation and down-regulation of cellular FLICE (FADD-like IL-1β-converting enzyme)-inhibitory protein ( Oh and Kwon, 2009 ; Patel et al., 2013 ; Um et al., 2012 ).
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Withaferin-A induced cell apoptosis mechanisms.
In a separate study on human cancer cells, the active withaferin-A from W. somnifera exhibits its cytotoxicity through Par-4 induction, through inhibition of chymotrypsin like activity of proteasome, and by covalently modifying the cysteine residue of intermediate filament protein vimentin. In addition, withaferin-A also induces actin microfilament aggregation by targeting Annexin-II ( Yang et al., 2013 ; Yu et al., 2010 ). On prostate cancer cells, withaferin-A arrests G2/M phase cell cycle and prevents mitosis by up regulation of phosphorylated Wee-1, phosphorylated histone H3, p21, and Aurora B targets. On the other hand, down regulation of cyclins (A2, B1, and E2) and a reduction in phosphorylated cyclin-dependent kinase (Cdc2) (Tyr15) were observed in in vitro studies and this suggests that activation of Cdc2 leads to arrest in the M phase of cell cycle, with abnormal duplication and initiation of mitotic catastrophe that result in cell death ( Roy et al., 2013 ). Withaferin-A also possesses its apoptotic action on human colon cancer cells through inhibition of Notch-1 signaling pathway and down regulating pro-survival pathways, such as Akt/NF-κB/Bcl-2, in three colon cancer cell lines (HCT-116, SW-480, and SW-620). It also induces apoptosis on colon cancer cells by other mechanisms like generating ROS ( Koduru et al., 2010 ). In addition, it also induces apoptosis in human breast cancer cells by mechanisms, such as inhibition of cell migration/invasion through down regulation of signal transducer and activator of transcription (STAT3) activity ( Patel et al., 2013 ). Suppression of X-linked inhibitor of apoptosis protein and cIAP-2 protein, and reduction in the survivin protein levels are also the common targets for withaferin-A to induce apoptosis on human breast cancer cells (MDA-MB-231 and MCF-7) ( Hahm and Singh, 2013 ). In a recent study, it was shown that withaferin-A inhibits the vimentin cytoskeleton through perinuclear vimentin accumulation followed by rapid vimentin depolymerization and a concomitant induction of vimentin ser 56 phosphorylation to induce apoptosis on human breast cancer cells ( Thaiparambil et al., 2013 ). Withaferin-A also reportedly increases ROS production due to inhibition of mitochondrial respiration resulting in apoptosis induction of breast cancer cells (MDA-MB-231 and MCF-7) ( Hahm et al., 2011 ). An investigation with malignant pleural mesothelioma (MPM) cells, indicates that withaferin-A inhibited growth of the MPM cells both in murine and human by decreasing the chymotryptic activity of the proteasome that results in elevation of ubiquitinated protein levels and pro-apoptotic proteasome target proteins (p21, Bax, IkBα). The apoptosis of MPM cells was induced by activation of pro-apoptotic p38 stress activated protein kinase and caspase-3, elevated levels of pro-apoptotic Bax protein and cleavage of poly-(ADP-ribose)-polymerase ( Yang et al., 2012 ). Withaferin-A also causes cytotoxicity in human renal carcinoma Caki cells, where studies show that it inhibits interleukin (IL)-6 induced phosphorylation of STAT3 via Tyr705 residue that resulted in reduction of Janus-activated kinase 2 activities. Withaferin-A also down-regulates the expression of STAT3 regulated genes such as Bcl-xL, Bcl-2, cyclin D1 and surviving which leads to cell apoptosis ( Um et al., 2012 ). In pancreatic cancer cell lines (Panc-1, MiaPaCa2 and BxPc3), withaferin A inhibits Hsp90 chaperone activity through an ATP independent mechanism, resulting in Hsp90 client protein degradation thus acting against pancreatic cancer ( Yu et al., 2010 ). In a variety studies, it was observed that W. somnifera significantly changed the levels of leucocytes, lymphocytes, neutrophils and immunoglobulins in experimental colon cancer in mice induced by azoxymethane ( Muralikrishnan et al., 2010a ). It was also observed that W. somnifera decreased the activities enzymes such as isocitrate dehydrogenase, succinate dehydrogenase, malate dehydrogenase and alpha-keto glutarate dehydrogenase in colon cancer bearing animals, leading to lack of nutrition of cancerous cells resulting in cell death ( Muralikrishnan et al., 2010b ). In high concentration, water extract of ashwagandha leaves induces apoptosis, cytotoxicity and cell death of human (YKG1, A172, U118MG) and rat (C6) glioma cell lines ( Kataria et al., 2011 ). Although both, withaferin-A and withanolides are extracted from W. somnifera , withaferin-A is the most potent anticancer compound than withanolides ( Kapoor, 2014 ). The results of the various findings have discovered that, W. somnifera and its chemical ingredients are effective in the prevention and treatment of several kinds of cancers including colon cancer, lung cancer, blood cancer, skin cancer, breast cancer, renal cancer, fibrosarcoma, prostate cancer and pancreatic cancer.
- Neuroprotective activity
Preclinical research and clinical trials support the use of W. somnifera for the treatment of neurological conditions such as anxiety, depression, cognitive disorders, senile dementia and neurodegenerative disorders (Alzheimer’s and Parkinson’s diseases). Earlier, it was reported that the neuroprotective activity of W. somnifera root extract could be because of presence of glycowithanolides and their ability to inhibit lipid peroxidation because of their antioxidant actions. In addition, withanolides and sitoindosides (VII-X) also augment catalase and glutathione peroxidase activities in rat frontal cortex and striatum. W. somnifera was also found to improve the cognitive capabilities of the brain by increasing the cortical muscarinic acetylcholine capacity in lateral septum and frontal cortex, which suggest their capacity to affect events in the cortical cholinergic-signal transduction cascade ( Schliebs et al., 1997 ). The pharmacological studies suggested that W. somnifera improves the athletic performance via increasing the hemoglobin count and red blood cell count, which leads to an increase in the capacity of blood to transport oxygen at a greater capacity to the peripheral system ( Shenoy et al., 2012 ). It has been shown that W. somnifera improves endurance performance in healthy individuals at a moderate intensity of 65% VO2 max ( Sandhu, 2010 ). W. somnifera which is rich in proteins, amino acids (glycine, alanine, tyrosine, aspartic acid, tryptophan, glutamic acid, cysteine, etc.), starch, reducing sugars, alkaloids, steroidal lactones possess an amazing nutritional value and acts as a tonic, stimulant and energy rejuvenator. Studies also revealed that, phenolic compounds present in the root of W. somnifera play an important role on overall antioxidant activities of the plant ( Bhatnagar et al., 2009 ).
Recent research developments in this area show different mechanisms ( Fig. 11 ) that help us understand the neuroprotective activity of W. somnifera and its bioactive withanolides.
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Neuroprotective mechanisms of Withania somnifera.
One such report has revealed that, W. somnifera root extract down-regulates nitric oxide production that significantly inhibits the stress induced NADPH-diaphorase activation in the brain via suppressing corticosterone release and activating cholineacetyltransferase. This pathway is thought to be the main mechanism underlying the neuroprotective effects of W. somnifera ( Bhatnagar et al., 2009 ). In another study W. somnifera root extract significantly increases the levels of brain antioxidant enzymes (superoxide dismutase (SOD), chloramphenicol acetyltransferase, glutathione, and glutathione S-transferase) and total proteins to protect the brain when animal was exposed to lead nitrate ( Sharma et al., 2011 ). Another report also revealed that withanolide-A isolated from roots of W. somnifera at a dose 10 μmol kg -1 could regenerate neurites and reconstruct synapses in severely damaged neurons which has a huge potential in the treatment of diabetic neuropathy ( Kuboyama et al., 2005 ). There is a scarcity of experimental data on the potential neuroprotective effects of W. somnifera against β-amyloid induced neuropathogenesis. However, in vitro studies with human neuronal SK-N-MC cell lines show that W. somnifera reverses the toxic effects when cells are intoxicated with β-amyloid (1-42) and HIV-1 Ba-L (clade B) infection ( Kurapati et al., 2013 ). Computational docking evidences reveal that withanolide-A inhibits brain acetyl cholinesterase, which could be a therapeutic alternative for the treatment of neurodegenerative Alzheimer’s disease ( Grover et al., 2012 ). The root of W. somnifera enriched with withanolides and withanosides reversed behavioral deficits, plaque pathology, accumulation of β-amyloid peptides and oligomers in the brains of middle-aged and old amyloid precursor protein/the presenilins Alzheimer's disease transgenic mice, results of this study indicates that W. somnifera increases the transport of β-amyloid peptides from the brain to the periphery. It also enhances the expression of low-density lipoprotein receptor-related protein in brain microvessels and the β-amyloid peptide-degrading protease neprilysin ( Sehgal et al., 2012 ). W. somnifera and its bioactive withanolides are also effective in treating Parkinson’s disease, where it was revealed that its root extract enhances brain dopamine level in Parkinson’s animals and also improves physiological abnormalities seen in Parkinson’s disease. W. somnifera improves the condition of lipidperoxidation, reduced glutathione content, activities of glutathione-S-transferase, glutathione reductase, glutathione peroxidase, superoxide dismutase and catalase, catecholamine content, dopaminergic D2 receptor binding affinity and tyrosine hydroxylase expression ( RajaSankar et al., 2009 ). Supplement with L-Dopa W. somnifera were also effective in inhibiting haloperidol-induced catalepsy in mice ( Girdhari et al., 2009 ). Randomized controlled clinical trial with W. somnifera root powder (3 g/day) also shows effectiveness in treating Parkinson’s disease in four weeks treatment. The results of the various findings described that, W. somnifera and its chemical ingredients are effective in prevention of neurodegenerative disorders and protect neurons from oxidative damages.
- Antiepileptic activity
W. somnifera is traditionally used for the treatment of epilepsy and seizures. Various in vitro and in vivo preclinical studies have provided enough evidence for the use of W. somnifera against various types of epilepsy. In general, studies with rodent models show that W. somnifera and its bioactive withanolides are effective in reducing seizures through various mechanisms. One such mechanism involved the Gama amino butyric acid (GABA) A receptor modulation in brain, where sub-effective dose of W. somnifera (50 mg/kg), with a sub-protective dose of either GABA (25 mg/kg) or Diazepm (0.5 mg/kg) increases the seizure threshold in brain ( Kulkarni et al., 2008 ). In another study, it was demonstrated that W. somnifera root extract and withanolide-A were capable of restoring spatial memory deficit by inhibiting oxidative stress induced alteration in glutamergic neurotransmission, where W. somnifera reduces the expression of N-metyl-D-aspartate (NMDA) receptor, which is responsible for spatial memory loss in epileptic rats ( Soman et al., 2012 ). Leaf extracts of W. somnifera were also showing its protective action against glutamate induced toxicity in human neuroblastoma (IMR-32) cells, by inhibiting over expression of stress protein 70 kilodalton heat shock proteins ( Kataria et al., 2012 ). In another study it was found that W. somnifera root extract and withanolide-A regulate the expression and function of α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor and glutamate levels in brain dopaminergic nervous system and results are attributed to improvement in motor learning in pilocarpine-induced temporal lobe epilepsy model ( Soman et al., 2013 ). These findings reveal that W. somnifera and its bioactive withanolides have anti convulsant potential and are useful in treating various types of epilepsy.
- Antidepression and antianxiety activity
The roots of W. somnifera are used extensively in Ayurveda for the treatment of anxiety and depression. Earlier it was reported that, anxiolytic-antidepressant potential of W. somnifera and its glycowithanolides ( Bhattacharya et al., 2000 ). Recent study reports also support the use of W. somnifera for depression and anxiety disorders. In a very recent study, it is found that W. somnifera at 40 mg/kg significantly reduces the depression in various experimental models ( Jayanthi et al., 2012 ). Clinical trials with healthy volunteers also revealed that aqueous extracts of W. somnifera improve the psychomotor performances in anxiety and depression ( Pingali et al., 2014 ). It was assumed that W. somnifera reduces the production of nitric oxide in the brain tissues, resulting in its anxiolytic activity ( Khan and Ghosh, 2011; Maity et al., 2011 ). Study findings explained that W. somnifera and its bioactive withanolides possesses antidepression and antianxiety potential and are useful in treating various types of mental disorders.
- Antiinflammatory and antiarthritic activity
W. somnifera exhibits potent antiarthritic and antiinflammatory activities. Antiinflammatory activity has been characteristic to biologically active steroids, of which withaferin-A is a major component. Recent studies revealed that W. somnifera at dose levels 600 & 800 mg/kg significantly decreased the severity of arthritis by effectively suppressing the inflammatory mediators and improving the functional recovery of motor activity in experimental animals ( Gupta and Singh, 2014 ). Roots of W. somnifera and with anolides are also effective in treating arthritic inflammation, inflammation in cystic fibrosis and irritable bowel syndrome, through various mechanisms such as inhibiting NF-κB activation, inhibition of COX-2 generation, inhibition of endothelial cell protein C receptor through antioxidant effect and cytokines release, thus in turn causes depletion of inflammatory mediators ( Ku et al., 2014 ; Mulabagal et al., 2009 ; Oh and Kwon, 2009 ). W. somnifera and its bioactive withaferin-A down regulate the production of inflammatory mediators like prostaglandins, histamine, interleukins and cytokines ( Gupta and Singh, 2014 ; Paval et al., 2009 ). Withaferin-A has been shown to stimulate differentiation and growth of osteoblasts in menopausal osteoporosis and by bone injury, via increased expression of osteoblast-specific transcription factor and mineralizing genes ( Khedgikar et al., 2013 ). Through all these mechanisms W. somnifera shows its antiinflammatory and antiarthritic activity, which makes it useful for the treatment of various inflammatory disorders. W. somnifera is also shown to possess analgesic activity in several rodent models and thus preferred for various pain management therapies ( Sabina et al., 2009 ; Shahriar et al., 2014 ).
- Spermatogenic activity
Several investigators reports have suggested that W. somnifera is beneficial in the treatment of male infertility. Experimental evidences have shown that treatment with W. somnifera induced testicular development and spermatogenesis in immature Wistar rats by directly affecting the seminiferous tubules, improved pro-sexual behavior of sexually sluggish mice, and increased testicular daily sperm production and serum testosterone level. W. somnifera , also counteract the oxidative damage to the sperm and reactive oxygen species associated with abnormal sperm parameters leading to infertility ( Ambiye et al., 2013 ). In recent years, it has been well documented that W. somnifera improves semen quality by effectively reducing oxidative stress and improving reproductive hormone levels in infertile male patients ( Ahmad et al., 2010 ; Shukla et al., 2011 ). In clinical trials with infertile male patients, W. somnifera repairs the altered concentrations of lactate, alanine, citrate, glycerylphosphorylcholine, histidine, and phenylalanine in seminal plasma, and it recovers the quality of semen of post-treated compared to pre-treated men, in addition to inducing spermatogenesis in infertile male patients ( Ambiye et al., 2013 ; Gupta et al., 2013 ). W. somnifera boosts enzymatic activity of metabolic pathways and energy metabolism. These evidences support the use of W. somnifera for the treatment of male infertility.
- Hepatoprotective activity
Various studies were performed to evaluate the hepatoprotective potential of W. somnifera . As it is used for various ailments, the hepatoprotective activity was also considered for its effective use. Investigations have given numerous evidences, where W. somnifera at a dose 500 mg/kg significantly reduces the elevated biomarkers (aspartate aminotransferase, alanine transaminase, alkaline phosphatase, and Bilirubin) in experimental animals when exposed to hepatotoxic dose of paracetamol. It significantly reduces the lipid peroxidation, enhances glutathione content, catalase, glutathione reductase and glutathione peroxidase activity in liver ( Malik et al., 2013 ; Sabina et al., 2013 ). In another study, W. somnifera has shown its hepatoprotective activity against gamma radiation induced toxicity in rodents, where 100 mg/kg dose of W. somnifera significantly decreases hepatic serum enzymes, levels of malondialdehyde, total nitrate/nitrite NO(x) and also heme oxygenase activity in liver. Serum antioxidant enzymes, including SOD and glutathione peroxidase in hepatic tissues were elevated ( Hosny and Farouk, 2012 ). These study findings support the use of W. somnifera for various hepatic disorders.
- Antimicrobial activity
The leaves and roots of W. somnifera have been shown to exhibit antimicrobial activity in recent studies. Leaf extracts at concentrations 6.25 mg/ml and 12.5 mg/ml inhibited the growth of five Gram-negative pathogenic bacteria ( Escherichia coli, Salmonella typhi, Citrobacter freundii, Pseudomonas aeruginosa and Klebsiella pneumonia ) ( Alam et al., 2012 ). Isolated flavonoids and alkaloids from W. somnifera show growth inhibitory activity against Enterobacter aerogens, Proteus mirabilis, Pseudomonas aeruginosa, Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, Raoultella planticola and Agrobacterium tumefaciens at concentration 0.039 mg/ml ( Singh and Kumar, 2011 ; Singh and Kumar, 2012 ). In a separate study, crude extract of leaves of W. somnifera was tested against clinical pathogens Staphylococcus aureus, roteus mirabilis Streptococcus mutans, Streptococcus sobrinus and Salmonella paratyphi B, where it was found that 100 μl of extracts (100 mg/ml) was able to inhibit the growth of all the pathogenic bacteria ( Al-Ani et al., 2013 ; Pandit et al., 2013 ). The antimicrobial potency of W. somnifera was thought to be due to its antioxidant properties ( Alam et al., 2012 ). The ascorbic acid, anthocyanin and polyphenols found in W. somnifera leaves could inhibit microorganisms via iron deprivation or hydrogen bonding with vital proteins such as microbial enzymes ( Scalbert, 1991 ). W. somnifera reported to exhibit antibacterial activities and it shows its activity against both Gram-positive and Gram-negative pathogenic bacteria ( Singariya et al., 2012 ). In another study, it was argued that W. somnifera shows its bactericidal and fungicidal activity through mechanisms attributed to cytotoxicity, gene silencing and immune potentiation, where aerial extract at concentration 1.56 mg/ml shows good antimicrobial potency ( Mwitari et al., 2013 ). It is also shown to be a moderate to active against Microsporum gypseum, Candida albicans and Cryptococcus neoformans ( Mwitari et al., 2013 ). Withanolide D, E and F showed potent activity against PknG target in Mycobacterium tuberculosis ( Santhi and Aishwarya, 2011 ). It has also been shown in different studies that W. somnifera have the best antimicrobial (1.5625 mg/ml), immunopotentiation (2 times IL-7 mRNA expression) and safety level (IC50 200 mg/ml). Results of these findings reveal that extracts of W. somnifera and its bioactive constituents possess great antimicrobial potential against various test pathogenic microorganisms that can be exploited for future antimicrobial drugs for treating infectious diseases and could be an alternative for chemotherapy.
- Hypoglycaemic and hypolipidemic activity
W. somnifera has long been used in traditional and Ayurvedic medicine to cure diabetes and obesity. Recent studies and observations have revealed that, flavonoids found in the roots of W. somnifera were able to reduce the high blood glucose level in experimental animals. It was also shown that W. somnifera at dose 100 mg/kg significantly reduces the blood glucose and lipid levels ( Rajangam, et al., 2009 ). In another study, powder of W. somnifera at dose 200 mg/kg significantly reduces the blood glucose level. The blood glucose lowering activity of W. somnifera is thought to be its action on pancreatic β-cells to stimulate the release of insulin. It was also found that W. somnifera and its glycowithanolides induce the transport of glucose into the cells, stimulate the release of insulin and increase the activity of GLUT transporters activity ( Anwer et al., 2008 ; Khalili, 2009 ; Sarangi et al., 2013 ; Visavadiya and Narasimhacharya, 2007 ). In another study it was observed that, W. somnifera diet significantly increases plasma HDL-cholesterol levels, increases HMG-CoA reductase activity and bile acid content of liver in experimental animals ( Visavadiya and Narasimhacharya, 2007 ). These observations support the traditional claims for the use of W. somnifera against diabetes and obesity.
- Miscellaneous pharmacological activities
In recent years, numerous pharmacological studies were also carried out to explore other beneficial effects of W. somnifera . Further research with withaferin-A shows that having antiplatelet, anticoagulant, and profibrinolytic properties ( Ku and Bae, 2014 ), cardioprotective activity, nephroprotective activity, immunomodulatory activity and antileishmanial activities. Details of various pharmacological activities are illustrated in Table 1 .
Reported pharmacological activities ofWithania somnifera
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Reported pharmacological activities of Withania somnifera
CONCLUSION
In the ancient system of Indian medicine, Withania somnifera is used as Rasayana herb for more than 2500 years. In many Ayurvedic formulations that are currently commercialized in India and other countries, W. somnifera participate as an active ingredient and are prescribed for treating various ailments that affects human health. Different parts of the plant has also been widely studied for their various pharmacological activities like anticancer, neuroprotective, antioxidant, anxiolytic, anti-depressant, adaptogen, memory enhancing, antiparkinsonian, antiinflammatory, and antitumor properties. Various other effects like immunomodulation, hypoglycemic, hypolipidemic, antibacterial, cardiovascular protection, or sexual behaviour have also been studied. Withanolides are among the most active constituents of W. somnifera with tremendous potential to treat various health disorders. The purification, structure characterization, and pharmacological studies on other classes of bioactive withanolides need further validation to support the traditional uses of withanolide-producing different parts of the plant to treat various ailments. Presence of diverse bioactive constituents and their low toxicity profiles, and novel mechanism of action makes ashwagandha a suitable drug candidate for the treatment of various diseases. However, there is a need of extensive research at the interface of chemistry and pharmacology to explore W. somnifera towards drug development with enhanced activity and lower toxicity, as compared to its available commercial formulations.
CONFLICT OF INTEREST The authors have no conflicting financial interests.
Acknowledgements
None.
References
Ahmad MK , Mahdi AA , Shukla KK , Islam N , Rajender S , Madhukar D , Shankhwar SN , Ahmad S 2010 Withania somnifera improves semen quality by regulating reproductive hormone levels and oxidative stress in seminal plasma of infertile males Fertil Steril 94 989 - 996    DOI : 10.1016/j.fertnstert.2009.04.046
Alam N , Hossain M , Mottalib Md A , Sulaiman SA , Gan SH , Khalil Md I 2012 Methanolic extracts of Withania somnifera leaves, fruits and roots possess antioxidant properties and antibacterial activities BMC Complement Altern Med 12 175 -    DOI : 10.1186/1472-6882-12-175
Al-Ani N , Hadi SA , Nazar R 2013 Antimicrobial activities of Withania somnifera Crude extract Sci Agri 4 74 - 76
Amaravathi P , Srilatha C , Ramadevi V , Sujatha K 2012 Immunomodulatory effect of Withania somnifera (ashwagandha) against fenvalerate induced immunotoxicity Int J Pharm Biol Sci 3 B10 - B16
Ambiye VR , Langade D , dongre S , aptikar P , Kulkarni M , Dongre A 2013 Clinical Evaluation of the Spermatogenic Activity of the Root Extract of Ashwagandha (Withania somnifera) in Oligospermic Males: A Pilot Study Evid Based Complement Alternat Med 2013 571420 -
Anwer T , Sharma M , Pillai KK , Iqbal M 2008 Effect of Withania somnifera on insulin sensitivity in non-insulin-dependent diabetes mellitus rats Basic Clin Pharmacol Toxicol 102 498 - 503    DOI : 10.1111/j.1742-7843.2008.00223.x
Baitharu I , Jain V , Deep SN , Hota KB , Hota SK , Prasad D , Ilavazhagan G 2013 Withania somnifera root extract ameliorates hypobaric hypoxia induced memory impairment in rats J Ethnopharmacol 145 431 - 441    DOI : 10.1016/j.jep.2012.10.063
Bhatnagar M , Sharma D , Salvi M 2009 Neuroprotective Effects of Withania somnifera Dunal.: A Possible Mechanism Neurochem Res 34 1975 - 1983    DOI : 10.1007/s11064-009-9987-7
Bhattacharya SK , Bhattacharya A , Sairam K. , Ghosal S 2000 Anxiolytic-antidepressant activity of Withania somnifera glycowithanolides: an experimental study Phytomedicine 7 463 - 469    DOI : 10.1016/S0944-7113(00)80030-6
Bhattacharya SK , Muruganandam AV 2003 Adaptogenic activity of Withania somnifera: An experimental study using a rat model of chronic stress Pharmacol Biochem Behav 75 547 - 555    DOI : 10.1016/S0091-3057(03)00110-2
Bone K 1996 Clinical Applications of Ayurvedic and Chinese Herbs: Monographs for the Western Herbal Practitioner Phytotherapy Press Warwick, Australia
Choudhary MI , Yousuf S , Rahman AU , Ramawat KG , Me'rillon JM 2013 Natural Products Springer-Verlag Berlin, Heidelberg Withanolides: Chemistry and Antitumor Activity 3465 - 3495
Devi PU , Sharada AC , Solomon FE , Kamath MS 1992 In vivo growth inhibitory effect of Withania somnifera (Ashwagandha) on a transplantable mouse tumor Sarcoma 180 Ind J Exp Biol 30 169 - 172
Elsakka M , Grigorescu E , Stănescu U , Stănescu U , Dorneanu V 1990 New data referring to chemistry of Withania somnifera species Rev Med Chir Soc Med Nat Iasi 94 385 - 387
Gardner Z , McGuffin M 2013 American Herbal Products Association’s Botanical Safety Hand Book CRC Press, Taylor & Francis Group Florida, United States
Girdhari LG , Avtar CR 2009 Synergistic effect of Withania somnifera dunal and L-dopa in the inhiition of haloperidol-induced catalepsy in mice Phcog Mag 19 46 - 50
Grover A , Shandilya A , Agrawal V , Bisaria VS , Sundar D 2012 Computational evidence to inhibition of human acetyl cholinesterase by withanolide A for Alzheimer treatment J Biomol Struct Dyn 29 651 - 662    DOI : 10.1080/07391102.2012.10507408
Gupta A , Mahdi AA , Shukla KK , Ahmad MK , Bansal N , Sankhwar P , Sankhwar SN 2013 Efficacy of Withania simnifera on seminal plasma metabolites of infertile males: a proton NMR study at 800 MHz J Ethnopharmacol 149 208 - 214    DOI : 10.1016/j.jep.2013.06.024
Gupta A , Singh S 2014 Evaluation of anti-inflammatory effect of Withania somnifera root on collaten-induced arthritis in rats Pharm Biol 52 308 - 320    DOI : 10.3109/13880209.2013.835325
Hahm ER , Moura MB , Kelley EE , Houten BV , Shiva S , Singh SV 2011 Withaferin-A-induced apoptosis in human breast cancer cells is mediated by reactive oxyge species PLoS One 6 e23354 -    DOI : 10.1371/journal.pone.0023354
Hahm ER , Singh SV 2013 Withaferin-A-induced apoptosis in human breast cancer cells is associated with suppression of inhibitor of apoptosis family protein expression Cancer Lett 334 101 - 108    DOI : 10.1016/j.canlet.2012.08.026
Hepper FN , Hawkes Lester , Nee Estrada 1991 Solanaceae III: Taxonomy, Chemistry, Evolution;Kew Bulletin Royal Botanic Gardens Kew and Linnean Society London, English Old World Withania (Solanaceae): A taxonomic review and key to the species 785 - 788
Hina S , Rehman KU , Dogar ZUH , Jahan N , Hameed M , Khan ZI , Ahmad K , Mukhtar K , Valeem E 2010 Cardioprotective effect of gemmotherapeutically treated Withania somnifera against chemically induced myocardial injury Pak J Bot 42 1487 - 1499
Hosny MH , Farouk HH 2012 Protective effect of Withania somnifera against radiation-induced hepatotoxicity in rats Ecotoxicol Environ Saf 80 14 - 19    DOI : 10.1016/j.ecoenv.2012.02.003
Ilayperuma I , Ratnasooriya WD , Weerasooriya TR 2002 Effect of Withania somnifera root extract on the sexual behaviour of male rats Asian J Androl 4 295 - 298
Jayanthi MK , Prathima C , Huralikuppi JC , Suresha RN , Dhar M 2012 Anti-depressant effects of Withania somnifera fat (Ashwagandha ghrutha) extract in experimental mice Int J Pharm Bio Sci 3 33 -
Joshi P , Misra L , Siddique AA , Kunar S , Darokar MP 2014 Epoxide group relationship with cytotoxicity in withanolide derivatives from Withania somnifera Steroids 79 19 - 27    DOI : 10.1016/j.steroids.2013.10.008
Kapoor S 2014 Withania somnifera and its emerging anti-neoplastic effects Inflammopharmacology 22 67 -    DOI : 10.1007/s10787-012-0162-4
Kataria H , Shah N , Kaul SC , Wadhwa R , Kaur G 2011 Water Extract of Ashwagandha Leaves Limits Proliferation and Migration, and Induces Differentiation in Glioma Cells Evid Based Complement Alternat Med 2011 267614 -
Kataria H , Wadhwa R , Kaul SC , Kaur G 2012 Water Extract from the Leaves of Withania somnifera Protect RA Differentiated C6 and IMR-32 Cells against Glutamate-Induced Excitotoxicity PLoS One 7 e37080 -    DOI : 10.1371/journal.pone.0037080
Khalili M 2009 The Effect of Oral Adminisration of Withania somnifera Root on Formalin-Induced Pain in Diabetic Rats Basic Clin Neurosci 1 29 - 31
Khan ZA , Ghosh AR 2011 L-Arginine abolishes the anxiolytic-like effect of withaferin-A in the elevated plus-maze test in rats Afr J Pharm Pharmacol 5 234 - 237    DOI : 10.5897/AJMR10.401
Khedgikar V , Kushwaha P , Gautam J , Verma A , Changkija B , Kumar A , Sharma S , Nagar GK , Singh D , Trivedi PK , Sangwan NS , Mishra PR , Trivedi R 2013 Withaferin A: a proteasomal inhibitor promotes healing after injury and exerts anabolic effect on osteoporotic bone Cell Death Dis 4 e778 -    DOI : 10.1038/cddis.2013.294
Koduru S , Kumar R , Srinivasan S , Evers MB , Damodaran C 2010 Notch-1 inhibition by Withaferin-A: a therapeutic target against colon carcinogenesis Mol Cancer Ther 9 202 - 210
Ku SK , Bae JS 2014 Antiplatelet, anticoagulant, and profibrinolytic activities of withaferin-A Vascul Pharmacol 60 120 - 126    DOI : 10.1016/j.vph.2014.01.009
Ku SK , Han MS , Bae JS 2014 Withaferin-A is an inhibitor of endothelial protein C receptor shedding in vitro and in vivo Food Chem Toxicol 6 23 - 29
Kuboyama T , Tohda C , Komatsu K 2005 Neuritic regeneration and synaptic reconstruction induced by withanolide A Br J Pharmacol 144 961 - 971    DOI : 10.1038/sj.bjp.0706122
Kulkarni SK , Akula KK , Dhir A 2008 Effect of Withania somnifera Dunal root extract against pentylenetetrazol seizure threshold in mice: possible involvement of GABAergic system Indian J Exp Biol 46 465 - 469
Kulkarni SK , Dhir A 2008 Withania somnifera: An Indian ginseng Prog Neuropsychopharmacol Biol Psychiatry 32 1093 - 1105    DOI : 10.1016/j.pnpbp.2007.09.011
Kurapati KRV , Atluri VSR , Samikkannu T , Nair MPN 2013 Ashwagandha (Withania somnifera) Reverses β-Anyloid 1-42 Induced Toxicity in Human Neuronal Cells: Implications in HIV-Associated Neurocognitive Disorders (HAND) PLoS One 8 e77624 -    DOI : 10.1371/journal.pone.0077624
Lavie D , Glotter E , Shvo Y 1965 Constituents of Withania somnifera Dun III. The side chain of withaferin A J Org Chem 30 1774 - 1778    DOI : 10.1021/jo01017a015
Mabberley DJ 2008 Mabberley's Plant-Book: a portable dictionary of plants, their classification and uses Cambridge University Press Cambridge, England
Maity T , Adhikari A , Bhattacharya K , Biswas S , Debnath PK , Maharana CS 2011 A study on evalution of antidepressant effect of Imipramine adjunct with Aswagandha and Bramhi Nepal Med College J 13 250 - 253
Malik T , Pandey DK , Dogra N 2013 Ameliorative Potential of Aqueous Root Extract of Withania somnifera Against Paracetamol Induced Liver Damage in Mice Pharmacologia 4 89 - 94    DOI : 10.5567/pharmacologia.2013.89.94
Manjunath M J 2013 Effect of Withania somnifera supplementation on rotenone-induced oxidative damage in cerebellum and striatum of the male mice brain Cent Nerv Syst Agents Med Chem 13 43 - 56    DOI : 10.2174/1871524911313010007
Mirjalili MH , Moyano E , Bonfill M , Cusido RM , Palazón J 2009 Steroidal Lactones from Withania somnifera, an Ancient Plant for Novel Medicine Molecules 14 2373 - 2393    DOI : 10.3390/molecules14072373
Mishra LC , Singh BB 2000 Scientific Basis for the Therapeutic Use of Withania somnifera (Ashwagandha): A Review Altern Med Rev 5 334 - 346
Mohanty I , Arya DS , Dinda A , Talwar KK , Joshi S , Gupta SK 2004 Mechanisms of cardioprotective effect of Withania somnifera in experimentally induced myocardial infarction Basic clin Pharmacol Toxicol 94 184 - 190
Motiwala HF , Bazzill J , Samadi A , Zhang H , Timmermann BN , Cohen MS , Aubé J 2013 Synthesis and Cytotoxicity of Semisynthetic Withalongolide A Analogues ACS Med Chem Lett 4 1069 - 1073    DOI : 10.1021/ml400267q
Mulabagal V , Subaraju GV , Rao CV , Sivaramakrishna C , DeWitt DL , Holnes D , Sung B , Aggarwal BB , Tsay HS , Nair MG 2009 Withanolide Sulfoxide from Aswagandha Roots Inhibits Nuclear Transcription Factor-Kappa-B, Cyclooxygenase and Tumor Cell Proliferation Phytother Res 22 987 - 992
Muralikrishnan G , Amanullah S , Basha MI , Dinda AK , Shakeel F 2010 Modulating effect of Withania somnifera on TCA cycle enzymes and electron transport chain in azoxymethane-induced colon cancer in mice Immunopharmacol Immunotoxicol 32 523 - 527    DOI : 10.3109/08923970903581540
Muralikrishnan G , Dinda AK , Shakeel F 2010 Immunomodulatory effects of Withania somnifera on azoxymethane induced experimental colon cancer in mice Immunol Invest 39 688 - 698    DOI : 10.3109/08820139.2010.487083
Mwitari PG , Ayeka PA , Ondicho J , Matu EN , Bii CC 2013 Antimicrobial activity and probable mechanisms of action of medicinal plants of Kenya: Withania somnifera, Warbugia ugandensis, Prunus africana and Plectrunthus barbatus PlosOne 8 e65619 -    DOI : 10.1371/journal.pone.0065619
Nema R , Khare S , Jain P , Pradhan A 2013 Anticancer activity of Withania somnifera (leaves) flavonoids compound Int J Pharm Sci Rev Res 19 103 - 106
Oh JH , Kwon TK 2009 Withaferin-A inhibits tumor necrosis factor alpha-induced expression of cell adhesion molecules by inactivation of Akt and NF-kappaB in human pulmonary epithelial cells Int Immunopharmacol 9 614 - 619    DOI : 10.1016/j.intimp.2009.02.002
Padmabathi B , Rath PC , Rao AR , Singh RP 2005 Roots of Withania somnbifera inhibit forestomach and skin carcinogenesis in mice Evid Based Complement Alternat Med 2 99 - 105    DOI : 10.1093/ecam/neh064
Pandit S , Chang KW , Jeon JG 2013 Effects of Withania somnifera on the growth and virulence properties of Streptococcus mutans and Streptococcus sobrinus at sub-MIC levels Anaerobe 19 1 - 8    DOI : 10.1016/j.anaerobe.2012.10.007
Pant M , Ambwani T , Umapathi V 2012 Antiviral Activity of Ashwagandha Extract on Infectious Bursal Disease Virus Replication Ind J Sci Tech 5 2750 - 2751
Patel K , Singh RB , Patel DK 2013 Pharmacological and analytical aspects of withaferin-A: A concise report of current scientific literature Asia Pac J Reproduction 2 238 - 243    DOI : 10.1016/S2305-0500(13)60154-2
Paval J , Kaitheri SK , Potu BK , Govindan S , Kumar RS , Narayanan SN , Moorkoth S 2009 Comparing the anti-arthritic activities of the plants Justicia gendarussa Burm F. and Withania somnifera Linn Int J Green Pharm 3 281 - 284    DOI : 10.4103/0973-8258.59732
Pingali U , Pilli R , Fatima N 2014 Effect of standardized aqueous extract of Withania somnifera on tests of cognitive and psychomotor performance in healthy human participants Pharmacognosy Res 6 12 - 18
Prabu PC , Panchapakesan S , Raj CD 2013 Acute and sub-acute oral toxicity assessment of the hydroalcoholic extract of Withania somnifera roots in Wistar rats Phytother Res 27 1169 - 1178    DOI : 10.1002/ptr.4854
Puri HS 2002 Rasayana: Ayurvedic Herbs for Longevity and Rejuvenation (Traditional Herbal Medicines for Modern Times) 1st ed. CRC press London, England
RajaSankar S , Manivasagam T , Sankar V , Prakash S , Muthusamy R , Krishnamurti A , Surendran S 2009 Withania somnifera root extract improves catecholamines and physiological abnormalities seen in a Parkinson's disease model mouse J Ethnopharmacol 125 369 - 373    DOI : 10.1016/j.jep.2009.08.003
Roy RV , Suman S , Das TP , Luevano JE , Damodaran C 2013 Withaferin-A a steroidal lactone from Withania somnifera, induces mitotic catastrophe and growth arrest in prostate cancer cells J Nat Prod 76 1909 - 1915    DOI : 10.1021/np400441f
Sabina EP , Chandel S , Rasool MK 2009 Evaluation of analgesic, antipyretic and ulcerogenic effect of Withaferin-A Int J Integr Biol 6 52 - 56
Sabina EP , Rasool M , Vedi M , Navaneethan D , Ravichander M , Parthasarthy P , Thella SR 2013 Hepatoprotective and antioxidant potential of Withania somnifera against paracetamol-induced liver damage in rats Int J Pharmacy Pharm Sci 5 648 - 651
Sachdeva H , Sehgal R , Kaur S 2013 Studies on the protective and immunomodulatory efficacy of Withania somnifera along with cisplatin against experimental visceral leishmaniasis Parasitol Res 112 2269 - 2280    DOI : 10.1007/s00436-013-3387-2
sandhu JS , Shah B , Shenoy S , Chauhan S , Lavekar GS , Padhi MM 2010 Effects of Withania somnifera (Ashwagandha) and Terminalia arjuna (Arjuna) on physical performance and cardiorespiratory endurance in healthy young adults Int J Ayurveda Res 1 144 - 149    DOI : 10.4103/0974-7788.72485
Santhi N , Aishwarya S 2011 Insights from the molecular docking of withanolide derivatives to the target protein PknG from Mycobacterium tuberculosis Bioinformation 7 1 - 4    DOI : 10.6026/97320630007001
Sarangi A , Jena S , Sarangi AK , Swain B 2013 Anti-diabetic effects of Withania somnifera root and leaf extracts on streptozotocin induced diabetic rats J Cell Tissue Res 13 3597 -
Scalbert A 1991 Antimicrobial properties of tannins Phytochem 30 3875 - 3883    DOI : 10.1016/0031-9422(91)83426-L
Schliebs R , Liebmann A , Bhattacharya SK , Kumar A , Ghosal S , Bigl B 1997 Systemic administration of defined extracts from Withania somnifera (Indian Ginseng) and Shilajit differentially affects cholinergic but not glutamatergic and GABAergic markers in rat brain Neurochem Int 30 181 - 190    DOI : 10.1016/S0197-0186(96)00025-3
Sehgal N , Gupta A , Valli RK , Datt Joshi S , Mills JT , Hamel E , Khanna P , Jain SC , Thakur SS , Ravindranath V 2012 Withania somnifera reverses Alzheimer's disease pathology by enhancing low-density lipoprotein receptor-related protein in liver Proc Natl Acad Sci USA 109 3510 - 3515    DOI : 10.1073/pnas.1112209109
Shahriar M , Alam F , Uddin MMN 2014 Analgesic and meuropharmacological activity of Withania somnifera root Int J Pharm 4 203 - 208
Sharada AC , Emerson Solomon F , Uma Devi P 1993 Toxicity of Withania somnifera root extract in rats and mice Pharm. Biol. 31 205 - 212    DOI : 10.3109/13880209309082943
Sharma S , Sharma V , Sharma S 2011 Therapeutic potential of hydromethanolic root extract of Withania somnifera on neurological parameters in swiss albino mice subjected to lead mitrate Int J Curr Pharm Res 3 52 - 56
Sharma U , Velpandian T , Sharma P , Singh S 2009 Evaluation of anti-leishmanial activity of selected Indian plants known to have antimicrobial properties Parasitol Res 105 1287 - 1293    DOI : 10.1007/s00436-009-1554-2
Shenoy S , Chaskar U , Sandhu JS , Paadhi MM 2012 Effects of eight-week supplementation of Ashwagandha on cardiorespiratory endurance in elite Indian cyclists J Ayurveda Integr Med 3 209 - 214    DOI : 10.4103/0975-9476.104444
Shimmi SC , Jahan N , Sultana N 2011 Effect of Ashwagandha (Withania somnifera) root extract against gentamicin induced changes of serum urea and creatinine levels in rats J Bangladesh Soc Physiol 6 84 - 89
Shukla KK , Mahdi AA , Mishra V , Rajender S , Sankhwar SN , Patel D , Das M 2011 Withania somnifera improves semen quality by combating oxidative stress and cell death and improving essential metal concentrations Reprod Biomed Online 22 421 - 427    DOI : 10.1016/j.rbmo.2011.01.010
Singariya P , Mourya KK , Kumar P 2012 Antimicrobial activity of the crude extracts of Withania somnifera and Cenchrus setigerus in vitro Phcog J 4 60 - 65    DOI : 10.5530/pj.2012.27.10
Singh B , Saxena AK , Chandan BK , Gupta DK , Bhutani KK , Anand KK 2001 Adaptogenic activity of a novel, withanolide free aqueous fraction from the roots of Withania somnifera Dun Phytother Res 15 311 - 318    DOI : 10.1002/ptr.858
Singh G , Kumar P 2012 Antibacterial potential of alkaloids of Withania somnifera L. & Euphorbia hirta L Int J Pharmacy Pharm Sci 4 78 - 81
Singh G , Kumar P 2011 Evaluation of antimicrobial efficacy of flavonoids of Withania somnifera L Indian J Pharm Sci 73 473 - 478
Singh N , Verma P , Pandey BR , Gilca M 2011 Role of Withania somnifera in prevention and treatment of cancer: An overview Int J Pharm Sci Drug Res 3 274 - 279
Singh SP , Tanwer BS , Khan M 2010 Antifungal potential of ashwagandha against some pathogenic fungi Int J Biopharm 1 72 - 74
Soman S , Anju TR , Jayanarayanan S , Antony S , Paulose CS 2013 Impaired motor learning attributed to altered AMPA receptor function in the cerebellum of rats with temporal lobe epilepsy: ameliorating effects of Withania somnifera and withanolide A Epilepsy Behav 27 484 - 491    DOI : 10.1016/j.yebeh.2013.01.007
Soman S , Korah PK , Jayanarayanan S , Mathew J , Paulose CS 2012 Oxidative stress induced NMDA receptor alteration leads to spatial memory deficits in temporal lobe epilepsy: ameliorative effects of Withania somnifera and withanolide A Neurochem Res 37 1915 - 1927    DOI : 10.1007/s11064-012-0810-5
Thaiparambil JT , Bender L , Ganesh T , Kline E , Patel P , Liu Y , Tighiouart M , Vertino PM , Harvey RD , Garcia A , Marcus AI 2011 Withaferin-A inhibits breast cancer invasion and metastasis at sub-cytotoxic doses by inducing vimentin disassembly and serine 56 phosphorylation Int J Cancer 129 2744 - 2755    DOI : 10.1002/ijc.25938
Udayakumar R , Kasthurirengan S , Mariashibu TS , Rajesh M , Anbazhagan VR , Kim SC , Ganapathi A , Choi CW 2009 Hypoglycaemic and hypolipidaemic effects of Withania somnifera root and leaf extracts on alloxan-induced diabetic rats Int J Mol Sci 10 2367 - 2382    DOI : 10.3390/ijms10052367
Um HJ , Min KJ , Kim DE , Kwon TK 2012 Withaferin-A inhibits JAK/STAT3 signaling and induces apoptosis of human renal carcinoma Caki cells Biochem Biophys Res Commun 427 24 - 29    DOI : 10.1016/j.bbrc.2012.08.133
Varma D , Kumar R , Namboothiri INN 2013 Synthesis of withasomnines and their non-natural analogues from aldehydes and 4-Nitro-1-butanol in three steps J Org Chem 78 3482 - 3486    DOI : 10.1021/jo400207u
Visavadiya NP , Narasimhacharya AV 2007 Hypocholesteremic and antioxidant effects of Withania somnifera (Dunal) in hypercholesteremic rats Phytomedicine 14 136 - 142    DOI : 10.1016/j.phymed.2006.03.005
Wadhwa R , singh R , Gao R , Shah N , Widodo N , Nakamoto T , Ishida Y , Terao K , Kaul SC 2013 Water extract of Ashwagandha leaves has anticancer activity: identification of an active component and its mechanism of action PLoS One 8 e77189 -    DOI : 10.1371/journal.pone.0077189
Wijeratne EM , Xu YM , Scherz-Shouval R , Marron MT , Rocha DD , Liu MX , Costa-Lotufo LV , Santagata S , Lindquist S , Whitesell L , Gunatilaka AA 2014 Structure-activity relationships for withanolides as inducers of the cellular heat-shock response J Med Chem 57 2851 - 2863    DOI : 10.1021/jm401279n
Yadav B , Bajaj A , Saxena M , Saxena AK 2010 In vitro anticancer activity of the Root, stem and leaves of Withania somnifera against various human cancer cell lines Indian J Pharm Sci 72 659 - 663    DOI : 10.4103/0250-474X.78543
Yang H , Wang Y , Cheryan VT , Wu W , Cui CQ , Polin LA , Pass HI , Dou QP , Rishi AK , Wali A 2012 Withaferin A inhibits the proteasome activity in mesothelioma in vitro and in vivo PLoS One 7 e41214 -    DOI : 10.1371/journal.pone.0041214
Yang Z , Garcia A , Xu S , Powell DR , Vertino PM , Singh S , Marcus AI 2013 Withania somnifera root extract inhibits mammary cancer metastasis and epithelial to mesenchymal transition PLoS One 8 e75069 -    DOI : 10.1371/journal.pone.0075069
Yu Y , Hamza A , Zhang T , Gu M , Zou P , Newman B , Li Y , Gunatilaka AA , Zhan CG , Sun D 2010 Withaferin A targets heat shock protein 90 in pancreatic cancer cells Biochem Pharmacol 79 542 - 551    DOI : 10.1016/j.bcp.2009.09.017