Javeed Ahmad Bhat
Tahira Akther
Rauf Ahmad Najar
Faheem Rasool5- 1Cancer Pharmacology Division, CSIR-Indian Institute of Integrative Medicine, Jammu, India
- 2Department of Biochemistry and Biophysics, University of Rochester, Rochester, NY, United States
- 3B. S. Abdur Rahman Crescent Institute of Science and Technology, Chennai, India
- 4Department of Pediatrics (Neonatology), Lung Biology and Disease Program, University of Rochester Medical Center, Rochester, NY, United States
- 5Government College for Women, Jammu, Jammu and Kashmir, India
- 6Department of Biotechnology, School of Life Sciences, Central University of Kashmir, Srinagar, India
Cancer and Neurodegenerative diseases are one of the most dreadful diseases to cure and chemotherapy has found a prime place in cancerous treatments while as different strategies have been tested in neurodegenerative diseases as well. However, due to adverse shortcomings like the resistance of cancerous cells and inefficiency in neurodegenerative disease, plant sources have always found a prime importance in medicinal use for decades, Withania somnifera (L.) Dunal (W. somnifera) is a well-known plant with medicinal use reported for centuries. It is commonly known as winter cherry or ashwagandha and is a prime source of pharmaceutically active compounds withanolides. In recent years research is being carried in understanding the extensive role of W. somnifera in cancer and neurological disorders. W. somnifera has been reported to be beneficial in DNA repair mechanisms; it is known for its cellular repairing properties and helps to prevent the apoptosis of normal cells. This review summarizes the potential properties and medicinal benefits of W. somnifera especially in cancer and neurodegenerative diseases. Available data suggest that W. somnifera is effective in controlling disease progressions and could be a potential therapeutic target benefiting human health status. The current review also discusses the traditional medicinal applications of W. somnifera, the experimental evidence supporting its therapeutical potential as well as obstacles that necessitate being overcome for W. somnifera to be evaluated as a curative agent in humans.
Introduction
A strong belief in traditional medicine has prompted the use of Nutraceuticals [like Withania Somnifera (L.) Dunal (W. somnifera), (Rivera et al., 2014; Heinrich et al., 2020), which has rigorously been used in Ayurveda] for enhancing general health status since ages and subsequent clinical evidence has turned this belief into practice, for instance at present dried powder capsules and alcohol derivatives are currently sold in the US market as drug supplement. This invite interest in exploring the efficacy of W. somnifera against challenging ailments including cancer chemoprevention which has tremendous room for discovering natural remedies even after a rich exploration in its direction for instance use of broccoli is suggested for the prevention of prostate cancer because of its bioactive constituent Sulforaphane. Ayurvedic drug Ashwagandha (W. somnifera), also known as Indian winter cherry and Indian ginseng, is a member of the Solanaceae family and has been used for thousands of years in India for its wide range of health benefits. Traditionally known as “ashwagandha,” was derived from the Sanskrit terms “ashva,” which means “horse,” and “gandha,” which means “smell,” and denotes the root’s aroma, which is similar to that of a horse. Sleep inducer is the species name “somnifera,” which highlights its critical role in stress relief. The plant is an upright, greyish, evergreen shrub with long tuberous roots, short stems, oblong, petiolate leaves, and greenish, bisexual flowers borne in the axils. Along with the drier regions of India, it can grow at high altitudes of 1700 m in the Himalayan region (mainly Himachal Pradesh, Uttarakhand, and Jammu and Kashmir). Despite the fact that there are 23 species of Withania identified, only W. somnifera and Withania. Coagulans (S) Dunal; W. coagulans (Rishyagandha) are thought to have therapeutic properties (Mirjalili et al., 2009b). Twenty-nine common metabolites generated from the leaf and root extracts have therapeutic significance in the form of flowers, roots, stems, and leaves. W. somnifera has been used as medicine since antiquity and has a long history, dating back to the year 6,000. Withanolides (Withaferin A, Withanolide A, Withanone), sitoindosides, Withanosides, and other alkaloids are the plant’s main metabolites, and they may have therapeutic and medical benefits (Figures 1, 2). It is used to treat a wide range of clinical disorders such as reducing blood sugar levels, depression, and stress, increasing energy, and enhancing cognitive function. In addition to its palliative effects, such as analgesic, rejuvenating, regenerating, and growth-promoting properties, this medicinal plant has been reported to be effective against epilepsy, inflammation, arthritis, depression, coagulation issues, free radicals, diabetes, and pyrexia. These therapeutic effects are partly attributable to W. somnifera’s potential to decrease reactive oxygen species, alter mitochondrial activity, regulate apoptosis, lower inflammation, and improve endothelial function by elevating the defense system. The first published report on the antibacterial activity of the W. somnifera plant dates back to 1958 (KURUP, 1958); later on, in 1960, the effect of whole plant extract of W. somnifera on the central nervous system (CNS) and skeletal muscles (Malhotra et al., 1960). Dhalla et al. (1961) first reported the chemotherapeutic properties of the extracts isolated from the leaves of W. somnifera. In a transplantable mouse tumor called Sarcoma 180, Devi et al., 1992 revealed for the first time in 1992 the in vivo growth inhibitory effects of plant root extracts of W. somnifera’s.
FIGURE 1. Phytochemicals from Withania somnifera.
FIGURE 2. Structure of different phytochemicals from Withania somnifera.
Withania somnifera in ayurveda
Although W. somnifera is more frequently employed in conventional medicine, W. coagulans is also used in some particular preparations (Upadhyay and Gupta, 2011). In more than 200 Ayurvedic compositions, W. somnifera roots are used. The powdered root of the W. somnifera plant known as ashwagandha is frequently used to cure several diseases. It is additionally combined with other compounds. The main ingredient in Saraswati churna, an herbal powder mixture intended to treat neurological problems, is W. somnifera. Another product that contains W. somnifera is ashwagandhadhi lehyam, which is generally used as an energy booster, a cure for male impotence, and a supplement for general rejuvenation (Rasheed et al., 2013). Even while these applications may appear to be very different, it’s conceivable that certain ratios and combinations with the other substances could provide very different results. It’s interesting to note that traditional medical treatments only use the plant’s root. Researchers in alternative medicine have lately examined the use of W. somnifera in Ayurvedic formulations and found that standardization, phytochemical screens, and testing for pathogen/heavy metal contamination can considerably enhance the effects of Ashwagandadhi lehyam. W. somnifera containing ayurvedic preparations are used as analgesics for a variety of musculoskeletal disorders (including arthritis and rheumatism), some types of hypertension, for inducing sex and boosting sperm counts, in gynecological practice for vaginitis, and during pregnancy for the development of the breasts (Mishra et al., 2000).
Withania somnifera and cancer
Cancer is a term used to refer to a wide range of illnesses and is distinguished by the rapid development of aberrant cells that proliferate uncontrollably. These aberrant cells typically upset the balance between cell proliferation and cell death, resulting in benign tumors that subsequently develop invasive characteristics and manifest symptoms of the disease that range from benign to metastatic (Bhat et al., 2017; Bisoyi, 2022). Most metastatic-stage malignancies are incurable and are the main reason for cancer-related deaths (Bano et al., 2020; Qadir Bhat et al., 2022). Genetic and environmental factors play a major role in how a normal cell becomes malignant. Physical carcinogens like UV and ionizing radiation, chemical carcinogens like asbestos, aflatoxin, and arsenic, and biological carcinogens including parasitic, bacterial, and viral infections are examples of external agents (Parsa, 2012). Mutations in the genes primarily responsible for cell survival, proliferation, and growth are brought on by these stimuli. One in six fatalities in 2018 were attributed to cancer, according to the WHO’s IARC (International Agency for Research on Cancer), which translates to 9.6 and 10 million deaths in 2018 and 2020, respectively. According to the IARC report 2020, there will be 30.2 million new cases of cancer worldwide by the year 2040, up from 19.3 million in 2020. India was expected to have 1,392,179 cancer patients by the year 2020, with men making up 679,421 (94.1 per 100,000) and women making up 712,758. (103.6 per 100,000). Lung, oral, prostate, tongue, and stomach cancers, which account for around 36% of all cancer cases in men, are the most often diagnosed cancers in these individuals, while as breast, cervix, uteri and lung constitute about 53% of all cancers in females (Mathur et al., 2020; Sung et al., 2021).
Of the many voids that still demand to be attended in the direction of research for battling and combating cancer is the safety and accuracy of drugs, a treatment that is free of side effects, being more precise. Heterogeneity exhibited by cancer cells, and a complexity associated with tumor interactions stands as a roadblock in the direction of efficacy of various therapies and this effort for exploring such drugs, has unraveled many naturally existing materials with anti-cancer activity and extracts of W. somnifera is a fine example.
W. somnifera is well studied herb and mounting evidence from in-vitro and in-vivo studies suggest that W. somnifera hosts anti-tumorigenic properties. The first experimental evidence in 1967, showed that W. somnifera root extract lowered cancer incidence in-vivo (Shohat et al., 1967) which centered research focus and interest in W. somnifera to explore its anti-tumor activity and direct towards its therapeutic potential till date. The anti-tumorigenic potential of W. somnifera prevail to its activity to speed up apoptotic cascade in cancer cells. The potential of cancer chemoprevention, cell survival and the activation of pro-apoptotic pathways needs successful reversal of the carcinogenesis that requires the early clearance or destruction of impaired cells. A plethora of in vitro evidence exists that validated that W. somnifera and its constituents like withanolides induce apoptosis (Srinivasan et al., 2007; Malik et al., 2009; Das et al., 2014). The earliest study of W. somnifera assess the potential role of leaf extract to inhibit tumor formation in mice which was subcutaneously injected with fibrosarcoma HT1080 cells (Widodo et al, 2007). In this study, it was concluded that mice treated with leaf extract (0.3 ml of 24 μg/ml extract in cell growth medium) attenuated tumor size via upregulation of p53. In another in vivo study it was observed that introduction of W. somnifera by intraperitoneal route (4 mg/kg body weight) 5 times for 2 weeks markedly suppresses MDA-MB-231 tumor weight as well as exhibited reduced cell proliferation and increased apoptosis compared with tumors from control mice (Stan et al., 2008b)In cervical cancer using xenograft mouse model, it was observed that i,p treatment of withaferin A (8 mg/kg body weight) for 6 weeks resulted in 70% reduction in tumor size compared to controls as well as heightened expression of p53 and lowered expression of pro-caspase 3/Bcl2(Munagala et al., 2011). In a study conducted on a xenograft mouse model of lung cancer, i,p administration of withaferin A (4 mg/kg body weight) reduced tumor volume by 60% (Gupta et al., 2012). The oral administration of withaferin A (5 mg/kg) prevents prostate adenocarcinoma, inhibit AKT signaling, and activate Foxo3a-Par-4-induced cell death and EMT markers (vimentin, β-catenin, and snail and upregulate E-cadherin) (Suman et al., 2016).
A wide range of cancers are treated using various therapeutics, either alone or in combination (Table 1). The potential of effective tumor treatments to interfere with tumor replication process, return normal cells to homeostasis with a minimum of side effects, and exhibit selectivity are among their most desirable pharmacological properties (Hussain et al., 2019; Nalli et al., 2019). The heterogeneity of cancer cells and complicated tumor interactions, which lead to clonal selection of a drug-resistant cell population, continue to limit the efficacy of many therapies despite significant efforts and the introduction of numerous chemotherapeutic drugs in the clinic. Due to their ability to target several cancer hallmarks, such as cell proliferation and death resistance, replicative capacity, and apoptosis, natural pharmaceutical compounds have attracted interest as chemotherapeutic agents to prevent or overcome treatment resistance.
TABLE 1. Preclinical status of Withaferin A in cancer.
Results from various animal studies and cell culture have highlighted anti-tumorigenic properties of W. somnifera. First demonstration of anti-cancerous properties of W. somnifera dates back to 1967 when root extracts were reported to lower incidence of cancer in vivo. This has attracted a trail of research interests and a timely revelation of its anti-tumorigenic properties. A hint of it can be inferred from a seemingly increase in publication number citing extracts of the plant over the past decade. It has been unraveled that anti-cancerous activity is not restricted to just roots but extends to scarcely used parts of the plant like leaf extracts. In a study by Wadhwa et al. (2013) a considerable anticancer activity was seen in water extracts of leaves of the plant. Metastasis, which is a hallmark of some cancer cells stands as a big hurdle in cancer therapies, and Withania is a good substitute to such therapies to curb the spread of cancer cells. Using vimentin as a pro metastatic protein, a decreased cell motility of breast tumor has been witnessed using different formulations of W. somnifera. Researchers went ahead and proved that inhibition of metastasis of breast cancer is associated with administration of root extracts of the plant with least severe effects in rats. A clear suggestion about potential of W. somnifera in regulation of G2/M cell cycle of tumor cells came out with an observation against prostate cancer that use of W. somnifera leads to metabolic inactivation of Cdc2 catastrophe and a subsequent cell death. Alkaloid extracts of W. somnifera mediates disruption of mitotic procedure by binding at the site of BIR5 protein and hence displays a potential for antitumor activity.
Although there are several chemoprotective medications available for the treatment of cancer, the most of them are quite expensive and have numerous adverse effects (Bayat Mokhtari et al., 2017). Therefore, it is vitally necessary to look for promising natural and cost-effective medications with minimal side effects to lower the morbidity rate. Cancer treatment with plant-based immunoprotective drugs is seen to be the most practical option (Ahmad et al., 2020). For these goals, a variety of plants with dietary origins, such as cruciferous vegetables, are employed (Greenwell and Rahman, 2015). They are more durable and have very few side effects. As a result, there is an urgent need for natural medicines that can stop the cancer-causing process.
The use of W. somnifera in cancer therapy has been extensively studied during the past 20 years. Initially, it was mostly used to treat concerns with conception and reproductive healthcare, but now, it is also used to prevent ageing, calm anxiety, increase vital fluid, semen, cell, blood, and lymph production, treat other health issues, and nourish various body parts (Singh et al., 2021).
The extensive phytochemistry of W. somnifera is what accounts for its multimodal actions. The therapeutic benefits of several metabolites are being researched. Withanolides are the main metabolites that demonstrate a variety of actions. The triterpenoids that make up the withanolides steroidal lactone backbone have about 28 carbons (Saggam et al., 2020). Phytochemicals known as withanolides are derived from the phytochemical ergostane, which is synthesized by plants utilizing isoprene units as precursor (Saleem et al., 2020). Additionally, sitoindosides is the name given to the glycolated withanolides. Carbon number 27 of Withaferin A has a β-D-glucopyranosyl residue that comes from sitoindoside IX (27-O-glucosylwithaferin A) (Mirjalili et al., 2009a). Sitoindoside X is created chemically by attaching palmitic acid to 27-O-glucosylwithaferin A. Similar to this, triethylene glycol and its derivatives have recently been discovered to be active W. somnifera components.
Numerous studies have reported that withaferin-A exerts anti-tumor activity through a number of mechanisms, including activation of the tumor suppressor protein (p53), antioxidant (ROS) signalling, activation of apoptosis, inhibition of epithelial-mesenchymal transition (EMT) signaling, decrease in phosphoinositide 3-kinase (PI3K) signaling, decrease in angiogenesis inhibition of Nuclear factor kappa B (NF-Kappa β) activation, decrease in notch signalling, altered cytoskeletal architecture, and downregulation of cell cycle proteins (cyclin B1, cyclin A, cdk2, expression of p-cdc), of oncoproteins, activation of tumor suppressor and anti-apoptotic proteins such as p53, Bcl 2, BAX, caspase 3, and cleaved poly-(ADP-ribose)-polymerase PARP (Sharma et al., 2014; Ahmad et al., 2017; Liu et al., 2019; Mallipeddi et al., 2021; Surya et al., 2021). W. somnifera extracts have shown potential for the treatment of a wide range of cancers, including those of the skin, breast, colon, liver and pancreatic (Najar et al., 2018) (Figure 3). W. somnifera root extract “priming” in HT-29 colon cancer cells boosted the effectiveness of the chemotherapy drug cisplatin which leads to mitochondrial dysfunction via increased ROS production (Henley et al., 2017). Leaf extracts of W. somnifera selectively kill the tumor cells by activating tumor suppressor protein p53 (Widodo et al., 2007). In pancreatic cancer cells, W. somnifera and some of its withanolides are reported to bind to HSP90 and decrease its chaperone function via an ATP-dependent mechanism (Yu et al., 2010b). The apoptosis induction, which is characterized by DNA condensation, cytoplasmic histone-associated DNA fragmentation, and cleavage of PARP, was connected with the withaferin A -mediated suppression of breast cancer cell survival (Dar et al., 2015, 2017; Ahmad and Dar, 2017). Withaferin A therapy decreases the expression of the NF-B and mTOR pathways in MDA-MB-231 and MCF-7 human breast cancer cell lines in a dose-dependent manner. These modifications significantly induced apoptosis, which was found to be correlated with upregulated Bax, Bim-s, Bim-L, Bim-EL and downregulated Bcl-2 protein expression. In vivo MDA-MB-231 xenograft suppression by withaferin A is accompanied by decreased cellular proliferation and enhanced apoptosis by FOXO3a and Bim (Stan et al., 2008b). Withaferin A shows anticancer activity in pancreatic cancer cell lines and in vivo pancreatic cancer xenografts via inhibition of Hsp90 in an ATP-independent manner which induces protein degradation and disrupts the Hsp90-Cdc37 interaction (Yu et al., 2010a). Combination of Withaferin A and oxaliplatin were used together to treat pancreatic cancer (PanCa), this led to intracellular ROS accumulation, which was correlated with Akt downregulation and apoptotic cell death (Bhat et al., 2021). This offered the strongest proof to yet of the combination therapy of withaferin A and oxaliplatin’s anticancer efficacy in PanCa therapy (Li et al., 2015). Withaferin A inhibits the progression of pancreatitis by blocking Endoplasmic Reticulum (ER) stress and the NLRP3 inflammasome (Kanak et al., 2017). Water extracts of W. somnifera has anticancer and antioxidant properties against Hepatocellular carcinoma (HCC) cell line HepG2 (Lin et al., 2017).
FIGURE 3. Effect of Withania somnifera on different pathways involved in Cancer.
Role of Withania somnifera in various neurodegenerative disorders
W. somnifera has been thoroughly studied during past few decades especially in neurodegenerative diseases (Table 2). Let’s analyze W. somnifera in neurodegenerative diseases in detail:
TABLE 2. Preclinical status of Withania Sominifera in neurodegenerative diseases.
Alzheimer’s disease
The most prevalent cause of dementia in senior people is Alzheimer’s disease (AD), a neurodegenerative condition that progresses over time and is histochemically characterized by extracellular amyloid beta (Aβ) protein deposits and intracellular neurofibrillary tangles in the cortical and limbic regions (Serrano-Pozo et al., 2011). Experimental models of AD’s behavioral impairments and clinical signs have been demonstrated to be reversed by W. somnifera extract. W. somnifera mediated reversal of amyloid induced toxicity in SK-N-MC neuronal cells and also reversed amyloid-induced reduction in spine density, spine area, spine length, and spine number, indicating protective impact of W. somnifera in AD (Dar and Ahmad, 2020). Moreover, W. somnifera supplementation reverses the effect of amyloid treatment in neuronal cells by inhibiting the acetylcholinesterase activity and reduction of amyloid-β internalization (Sehgal et al., 2012; Kurapati et al., 2013). Bioinformatics studies have revealed the mechanism by which inhibitory effect of Withanolide A in AD. Withanolide A binds to the different residues of acetylcholinesterase enzyme (such as Thr78, Trp81, Ser120, and His442). These residues are present in the active site and play a pivotal role in proper functioning of acetylcholinesterase enzyme (Grover et al., 2012). Cell death caused by the amyloid toxicity in PC-12 cells is abrogated by the treatment of Withaferin A and C. These Withanamides blocks the active site of β-amyloid and inhibits the fibril formation (Jayaprakasam et al., 2010). Root extracts of W. somnifera orally administered to Alzheimer’s transgenic mice reverse the accumulation of Aβ and behavioral deficits by upregulation of low density lipoprotein receptor-related protein (LRP) (Sehgal et al., 2012). Behavioral deficits or cognitive defects induced by Bisphenol A (BPA) and ibotenic in Swiss albino mice are reversed by the treatment of W. somnifera by restoring NMDA receptors (Singh et al., 2011; Birla et al., 2019). W. somnifera’s root aqueous extract functions as a neuroprotective agent by shielding PC-12 cells from the cytotoxicity brought on by Aβ (1–42) and H2O2 (Kumar et al., 2010a). Withanolide A also protects the AD by increasing the expression of neuroprotective protein hemeoxygenase-1 (Nitti et al., 2018). Withanolide A may benefit AD by promoting neuritogenic activity and inhibiting secretase activity (Strooper et al., 2010). People with MCI may benefit from Ashwagandha’s potential to improve executive function, attention, and the speed at which information is processed (Choudhary et al., 2017). W. somnifera extracts can enhance memory and cognitive performance by modifying cholinergic neurotransmission (Pingali et al., 2014). In addition, high resolution Q-TOF/MS research has demonstrated that the Withanamides in W. somnifera fruit extract crossed the blood-brain barrier in mice after intraperitoneal administration, suggesting that oral administration of the extract could result in effects similar to those seen after intraperitoneal administration because the extract has functionalities that are both lipophilic and hydrophilic and easily crosses membranes (Vareed et al., 2014).
Parkinson’s disease
Parkinson’s disease (PD) is a neurodegenerative motor disorder marked by the loss of dopaminergic neurons in the substantia nigra (Wongtrakul et al., 2021). Development of PD is caused by decreased dopamine levels in brain areas controlling motor activities (Mazzoni et al., 2012). PD has been linked to impaired anti-oxidative defense mechanisms and increased production of oxidative free radicals. Dysregulation of glutathione peroxidase (GPX), catalase, and superoxide dismutase (SOD) increases harmful free radicals build up and the disease progresses in a degenerative way (Maxwell, 1995). Pretreatment of W. somnifera extracts in hydroxyl dopamine (6-OHDA) Parkinson disease rat model does not alter the expression of antioxidant enzymes such as catalase, tyrosine hydroxylase, glutathione peroxidase, and SOD (Ahmad et al., 2005). The 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)PD model treated with W. somnifera (100 mg/kg body weight) for 7 or 28 days showed higher expression of DA, HVA, and DOPAC when compared with control MPTP PD model (RajaSankar et al., 2009). Ethanolic root extracts of W. somnifera treatment provides nigrostriatal dopaminergic neuroprotection against MB–PQ induced Parkinsonism by the reducing the expression of iNOS (an oxidative stress marker oxidative stress) and antiapoptotic proteins such as Bax and Bcl-2 (Prakash et al., 2014).
Huntington’s disease
Huntington’s disease (HD) is a deadly neurodegenerative disorder that results from the destruction of neurons in the basal ganglia. HD selectively targets striatal spiny projection neurons (Choudhary et al., 2013). Progressive motor dysfunction, such as chorea and dystonia, emotional issues, memory problems, and weight loss are the hallmarks of HD. It is generally known that GABAergic system has a role in the pathogenesis of HD, and it is also well known that W. somnifera acts through GABAergic system. In mice treated with 3-nitropropionic acid (3-NP), W. somnifera root extract pretreatment dramatically recovered glutathione enzyme level system, acetyl cholinesterase enzyme activity, and cognitive function (Kumar and Kumar, 2009). In a 3-NP-induced model of HD, W. somnifera root extract has been shown to significantly improve cognitive behavior (as measured by the Morris Water Maze and Elevated Plus Maze tests) and motor (impairment of muscle activity as measured by the Rotarod and Limb Withdrawal Tests) activities. This improvement has been attributed to the inhibition of oxidative stress, restoration of antioxidant status, and enhancement of acetylcholinesterase enzyme activity on W. somnifera supplementation (Paul et al., 2021).
Cerebral ischemia
Stroke is one of the leading causes of brain injury for millions of individuals worldwide. About 87% of strokes are ischemic strokes (Go et al., 2014). W. somnifera pre-supplementation (50 mg/kg) reduced the reperfusion injury-induced biochemical and histological changes in a rat model of bilateral common carotid artery blockage. In a different study, it was discovered that pre-supplementing with W. somnifera reduced oxidative stress, lesion volume, and restored neurological impairments in the middle cerebral artery occlusion (MCAO) stroke model (Choudhary et al., 2013). Additionally, W. somnifera dramatically reduced the size of the cerebral infarct and improved the histological changes in MCAO mice. Hemeoxygenase 1 (HO1) expression was found to be upregulated by W. somnifera treatment, which also attenuated the expression of the PARP1 via the PARP1-AIF pathway, preventing the nuclear translocation of apoptosis-inducing factor (AIF), suggesting involvement of anti-apoptotic pathways and angiogenesis (Raghavan and Shah, 2015). Stroke, multiple sclerosis, brain injuries, and neurodegenerative diseases have all been linked to glutamate neurotoxicity. Inhibition of glutamate-induced neurotoxicity by a water extract from the leaves of W. somnifera has been seen in retinoic acid differentiated rat glioma (C6) and human neuroblastoma (IMR-32) cells (Kataria et al., 2012). Withanolide A reverses the hippocampus’s hypoxia-induced glutathione depletion and slows the progression of neurodegeneration. Additionally, withanolide A promoted glutamate-cysteine ligase (GCLC) levels through the Nrf2 pathway in a corticosteroid-dependent manner, increasing glutathione production in neuronal cells (Baitharu et al., 2014).
Epilepsy
Epilepsy is a cognitive condition brought on by excessive neurotransmitter release. Depression, anxiety, and epilepsy are all prevalent conditions. Therefore, it is not surprising that a sizable number of people have both illnesses. Indeed, according to some experts, up to 55% of people with epilepsy will experience depression at some point in their lifetime (Jackson, 2005). Because so many people worldwide suffer from seizure disorders and there are so few effective treatments available, this condition is regarded as a major health problem. Around 15 million epileptic patients worldwide do not react to any of the treatments that are now available. Recurrent seizures are the hallmark of epilepsy. Glutamate and gamma amino butyric acid (GABA) are reported to play pivotal roles in the disordered balance of stimulatory and inhibitory neurotransmitters, which is the main cause of epilepsy (Barker-Haliski and White, 2015). W. somnifera shows anticonvulsant properties against pentylenetetrazol (PTZ) seizure threshold paradigm involved the GABAAergic modulation. W. somnifera (100 or 200 mg/kg) increases the PTZ threshold. Co administration of W. somnifera (50 mg/kg) with GABA (25 mg/kg) or diazepam (0.5 mg/kg) increased the seizure threshold (Kulkarni et al., 2008). The GABA receptor’s function is modulated and interfered by W. somnifera activating chloride channels, which increases the seizure threshold. The GABAergic neurotransmitter system is therefore most likely the fundamental mechanism by which the W. somnifera root extract raises the threshold of PTZ-induced seizure (Isoherranen et al., 2003). Co-administration of W. somnifera and Flax seed oil significantly reduces the convulsion phase in rats experiencing MES seizures (Tanna et al., 2012). Aqueous seed extracts of W. somnifera possess anti-convulsant by modulating the dopamine and serotonin levels in hippocampus of pilocarpine induced rat models (300 mg/kg) (Costa et al., 2012). Figures 4, 5 represents the effect of W. somnifera on different neurodegenerative diseases. W. somnifera produces bioactive natural chemicals that are rich in phenols, steroids, and flavonoid molecules and have good biocompatibility, bioavailability, and low toxicity. By regulating the endocrine, cardiac, central nervous system, and sexual behavior without causing any harm, Ashwagandha demonstrates a wide spectrum of therapeutic qualities. The root has been used most commonly for medicinal purposes and is a component of more than 200 Ayurvedic, Siddha, and Unani medicine formulations. Modern scientific research suggests that the aerial parts of the plant, such as its leaves, stem, fruit, and seeds, also possess several biologically active metabolites, despite the fact that the roots of the W. somnifera plant are the primary source of traditional Ayurvedic formulations. W. somnifera has been found to contain more than 40 withanolides, 12 alkaloids, and uncommon sitoindosides. The safety and clinical effectiveness of W. somnifera were documented in a total of 69 trials (30 clinical and 39 preclinical) (Kashyap et al., 2020). Numerous studies have reported that different parts of the plant have been linked to a variety of preclinical experiments, including cardioprotective (Khalil et al., 2015), anticancer (Alfaifi et al., 2016), antioxidant (Ahmed et al., 2018), antibacterial (Alam et al., 2012), antifungal (Bisht and Rawat, 2014), anti-inflammatory (Sahni and Srivastava, 1993), hepatoprotective (Sharma et al., 2021), anti-depressant (Bhattacharya et al., 2000), and hypoglycemic effects (Udayakumar et al., 2009). In a TPA-induced mice psoriatic-like paradigm, the concomitant administration of W. somnifera seed fatty acids decreased psoriatic lesions and skin inflammation. Extracts from seeds of W. somnifera has been shown to have potent anti-inflammatory activities by modifying NFκB activity and reducing the production of pro-inflammatory cytokines, such as IL-6 and TNF-, in cell-based experiments that were triggered by either TPA or LPS (Balkrishna et al., 2020).
FIGURE 4. Effect of Withania somnifera on different neurodegenerative diseases.
FIGURE 5. Overview of Withania somnifera on neurodegenerative diseases.
Future prospects
W. somnifera is one of the most widely used plant in Indian System of Medicine for several ailments and the claims for its use to improve a myriad of clinical conditions are overwhelmingly encouraging as a multi-purpose medicinal agent. However, at present given the paucity of randomized clinical trials (RCTs) there are insignificant number of clinically proven reports to justify its general medical use. We believe some of the questions are immediately warranted and are necessary before clinical recommendations on W. somnifera could be made confidently. Extracts of W. somnifera have been extensively studied in preclinical in-vitro and in-vivo models, demonstrating numerous molecular targets of W. somnifera and its effects in attenuating several dysfunctions and diseases in humans. But there are no comprehensive studies to decipher the effect of the active constitutes, rather there is a dichotomy in results in relation to several human disorders which could be answered by designing a well-regulated larger cohort of studies to analyze the effect of this potential drug candidate.
Author contributions
JB and AH contributed in framing the outline of the manuscript. While as JB and TA wrote the manuscript, JB, RN, and FR contributed for figures.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
Abu Bakar, M. H., Azmi, M. N., Shariff, K. A., and Tan, J. S. (2019). Withaferin A protects against high-fat diet–induced obesity via attenuation of oxidative stress, inflammation, and insulin resistance. Appl. Biochem. Biotechnol. 188, 241–259. doi:10.1007/s12010-018-2920-2
Ahmad, M., Aga, M. A., Bhat, J. A., Kumar, B., Rouf, A., Capalash, N., et al. (2017). Exploring derivatives of quinazoline alkaloid l-vasicine as cap groups in the design and biological mechanistic evaluation of novel antitumor histone deacetylase inhibitors. J. Med. Chem. 60, 3484–3497. doi:10.1021/acs.jmedchem.7b00322
Ahmad, M., and Dar, N. J. (2017). “Withania somnifera,” in Sustained energy for enhanced human functions and activity (Elsevier), 137–154. doi:10.1016/B978-0-12-805413-0.00008-9
Ahmad, M., Saleem, S., Ahmad, A. S., Ansari, M. A., Yousuf, S., Hoda, M. N., et al. (2005). Neuroprotective effects of Withania somnifera on 6-hydroxydopamine induced Parkinsonism in rats. Hum. Exp. Toxicol. 24, 137–147. doi:10.1191/0960327105ht509oa
Ahmad, S. M., Nayak, D., Mir, K. B., Faheem, M. M., Nawaz, S., Yadav, G., et al. (2020). Par-4 activation restrains EMT-induced chemoresistance in PDAC by attenuating MDM-2. Pancreatology 20, 1698–1710. doi:10.1016/j.pan.2020.09.021
Ahmed, W., Mofed, D., Zekri, A.-R., El-Sayed, N., Rahouma, M., and Sabet, S. (2018). Antioxidant activity and apoptotic induction as mechanisms of action of Withania somnifera (Ashwagandha) against a hepatocellular carcinoma cell line. J. Int. Med. Res. 46, 1358–1369. doi:10.1177/0300060517752022
Alam, N., Hossain, M., Mottalib, M. A., Sulaiman, S. A., Gan, S. H., and Khalil, M. 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
Alfaifi, M. Y., Saleh, K. A., El-Boushnak, M. A., Elbehairi, S. E. I., Alshehri, M. A., and Shati, A. A. (2016). Antiproliferative activity of the methanolic extract of Withania somnifera leaves from faifa mountains, southwest Saudi arabia, against several human cancer cell lines. Asian pac. J. Cancer Prev. 17, 2723–2726. Available at: http://www.ncbi.nlm.nih.gov/pubmed/27268658.
Atluri, V. S. R., Tiwari, S., Rodriguez, M., Kaushik, A., Yndart, A., Kolishetti, N., et al. (2020). Inhibition of amyloid-beta production, associated neuroinflammation, and histone deacetylase 2-mediated epigenetic modifications prevent neuropathology in Alzheimer’s disease in vitro model. Front. Aging Neurosci. 11, 342. doi:10.3389/fnagi.2019.00342
Baitharu, I., Jain, V., Deep, S. N., Shroff, S., Sahu, J. K., Naik, P. K., et al. (2014). Withanolide A prevents neurodegeneration by modulating hippocampal glutathione biosynthesis during hypoxia. PLoS One 9, e105311. doi:10.1371/journal.pone.0105311
Balkrishna, A., Nain, P., Chauhan, A., Sharma, N., Gupta, A., Ranjan, R., et al. (2020). Super critical fluid extracted fatty acids from Withania somnifera seeds repair psoriasis-like skin lesions and attenuate pro-inflammatory cytokines (TNF-α and IL-6) release. Biomolecules 10, 185. doi:10.3390/biom10020185
Bano, N., Hossain, M. M., Bhat, A. Q., Ayaz, M. O., Kumari, M., Sandhu, P., et al. (2020). Analyzing structural differences between insulin receptor (IR) and IGF1R for designing small molecule allosteric inhibitors of IGF1R as novel anti-cancer agents. Growth Horm. IGF Res. 55, 101343. doi:10.1016/j.ghir.2020.101343
Barker-Haliski, M., and White, H. S. (2015). Glutamatergic mechanisms associated with seizures and epilepsy. Cold Spring Harb. Perspect. Med. 5, a022863. doi:10.1101/cshperspect.a022863
Bayat Mokhtari, R., Homayouni, T. S., Baluch, N., Morgatskaya, E., Kumar, S., Das, B., et al. (2017). Combination therapy in combating cancer. Oncotarget 8, 38022–38043. doi:10.18632/oncotarget.16723
Bhat, A. Q., Ayaz, M. O., Hossain, M. M., Maqsood, A., and Dar, M. J. (2021). Handbook of oxidative stress in cancer: Mechanistic aspects. Singapore: Springer Singapore, 1–17. doi:10.1007/978-981-15-4501-6_188-1Impact of ROS on cancer and stem cell growth and therapeutics
Bhat, J. A., Ahmad, M., Dar, N. J., Hussain, A., Najar, R. A., Sharma, S., et al. (2017). Abstract 1376: Novel HDAC inhibitor SBAK-GHA: Potential therapuetic molecule for lymophocytic leukaemia. Cancer Res. 77, 1376. doi:10.1158/1538-7445.AM2017-1376
Bhattacharya, S. K., Bhattacharya, A., Sairam, K., and 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
Birla, H., Keswani, C., Rai, S. N., Singh, S. S., Zahra, W., Dilnashin, H., et al. (2019). Neuroprotective effects of Withania somnifera in BPA induced-cognitive dysfunction and oxidative stress in mice. Behav. Brain Funct. 15, 9. doi:10.1186/s12993-019-0160-4
Bisht, P., and Rawat, V. (2014). Antibacterial activity of Withania somnifera against Gram-positive isolates from pus samples. Ayu 35, 330–332. doi:10.4103/0974-8520.153757
Bisoyi, P. (2022). “A brief tour guide to cancer disease,” in Understanding cancer (Elsevier), 1–20. doi:10.1016/B978-0-323-99883-3.00006-8
Cai, Y., Sheng, Z.-Y., Chen, Y., and Bai, C. (2014). Effect of withaferin A on A549 cellular proliferation and apoptosis in non-small cell lung cancer. Asian pac. J. Cancer Prev. 15, 1711–1714. doi:10.7314/APJCP.2014.15.4.1711
Chang, E., Pohling, C., Natarajan, A., Witney, T. H., Kaur, J., Xu, L., et al. (2016). AshwaMAX and Withaferin A inhibits gliomas in cellular and murine orthotopic models. J. Neurooncol. 126, 253–264. doi:10.1007/s11060-015-1972-1
Choi, M. J., Park, E. J., Min, K. J., Park, J.-W., and Kwon, T. K. (2011). Endoplasmic reticulum stress mediates withaferin A-induced apoptosis in human renal carcinoma cells. Toxicol. Vitro 25, 692–698. doi:10.1016/j.tiv.2011.01.010
Choudhary, D., Bhattacharyya, S., and Bose, S. (2017). Efficacy and safety of ashwagandha (Withania somnifera (L.) dunal) root extract in improving memory and cognitive functions. J. Diet. Suppl. 14, 599–612. doi:10.1080/19390211.2017.1284970
Choudhary, S., Kumar, P., and Malik, J. (2013). Plants and phytochemicals for Huntington’s disease. Pharmacogn. Rev. 7, 81–91. doi:10.4103/0973-7847.120505
Costa, J. P., Ferreira, P. B., De Sousa, D. P., Jordan, J., and Freitas, R. M. (2012). Anticonvulsant effect of phytol in a pilocarpine model in mice. Neurosci. Lett. 523, 115–118. doi:10.1016/j.neulet.2012.06.055
Dar, N. J., Bhat, J. A., Satti, N. K., Sharma, P. R., Hamid, A., and Ahmad, M. (2017). Withanone, an active constituent from Withania somnifera, affords protection against NMDA-induced excitotoxicity in neuron-like cells. Mol. Neurobiol. 54, 5061–5073. doi:10.1007/s12035-016-0044-7
Dar, N. J., Hamid, A., and Ahmad, M. (2015). Pharmacologic overview of Withania somnifera, the Indian ginseng. Cell. Mol. Life Sci. 72, 4445–4460. doi:10.1007/s00018-015-2012-1
Dar, N. J., and Ahmad, M. (2020). Neurodegenerative diseases and Withania somnifera (L.): An update. J. Ethnopharmacol. 256, 112769. doi:10.1016/j.jep.2020.112769
Das, R., Rauf, A., Akhter, S., Islam, M. N., Emran, T. B., Mitra, S., et al. (2021). Role of withaferin A and its derivatives in the management of Alzheimer’s disease: Recent trends and future perspectives. Molecules 26 (12), 3696. doi:10.3390/molecules26123696
Das, T., Roy, K. S., Chakrabarti, T., Mukhopadhyay, S., and Roychoudhury, S. (2014). Withaferin A modulates the Spindle Assembly Checkpoint by degradation of Mad2–Cdc20 complex in colorectal cancer cell lines. Biochem. Pharmacol. 91, 31–39. doi:10.1016/j.bcp.2014.06.022
Devi, P. U., Sharada, A. C., Solomon, F. E., and Kamath, M. S. (1992). In vivo growth inhibitory effect of Withania somnifera (Ashwagandha) on a transplantable mouse tumor, Sarcoma 180. Indian J. Exp. Biol. 30, 169–172.
Dhalla, N. S., Sastry, M. S., and Malhotra, C. L. (1961). Chemical studies of the leaves of Withania somnifera. J. Pharm. Sci. 50, 876–877. doi:10.1002/jps.2600501019
Fong, M. Y., Jin, S., Rane, M., Singh, R. K., Gupta, R., and Kakar, S. S. (2012). Withaferin A synergizes the therapeutic effect of doxorubicin through ROS-mediated autophagy in ovarian cancer. PLoS One 7, e42265. doi:10.1371/journal.pone.0042265
Go, A. S., Mozaffarian, D., Roger, V. L., Benjamin, E. J., Berry, J. D., Blaha, M. J., et al. (2014). Heart disease and stroke statistics--2014 update: A report from the American heart association. Circulation 129, e28–e292. doi:10.1161/01.cir.0000441139.02102.80
Greenwell, M., and Rahman, P. K. S. M. (2015). Medicinal plants: Their use in anticancer treatment. Int. J. Pharm. Sci. Res. 6, 4103–4112. doi:10.13040/IJPSR.0975-8232.6(10).4103-12
Grogan, P. T., Sleder, K. D., Samadi, A. K., Zhang, H., Timmermann, B. N., and Cohen, M. S. (2013). Cytotoxicity of withaferin A in glioblastomas involves induction of an oxidative stress-mediated heat shock response while altering Akt/mTOR and MAPK signaling pathways. Invest. New Drugs 31, 545–557. doi:10.1007/s10637-012-9888-5
Grover, A., Shandilya, A., Agrawal, V., Bisaria, V. S., and 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, R. C., Bansal, S. S., Aqil, F., Jeyabalan, J., Cao, P., Kausar, H., et al. (2012). Controlled-release systemic delivery - a new concept in cancer chemoprevention. Carcinogenesis 33, 1608–1615. doi:10.1093/carcin/bgs209
Heinrich, M., Appendino, G., Efferth, T., Fürst, R., Izzo, A. A., Kayser, O., et al. (2020). Best practice in research – overcoming common challenges in phytopharmacological research. J. Ethnopharmacol. 246, 112230. doi:10.1016/j.jep.2019.112230
Henley, A. B., Yang, L., Chuang, K.-L., Sahuri-Arisoylu, M., Wu, L.-H., Bligh, S. W. A., et al. (2017). Withania somnifera root extract enhances chemotherapy through ‘priming. PLoS One 12, e0170917. doi:10.1371/journal.pone.0170917
Heyninck, K., Lahtela-Kakkonen, M., Van der Veken, P., Haegeman, G., and Vanden Berghe, W. (2014). Withaferin A inhibits NF-kappaB activation by targeting cysteine 179 in IKKβ. Biochem. Pharmacol. 91, 501–509. doi:10.1016/j.bcp.2014.08.004
Hsu, J. H.-M., Chang, P. M.-H., Cheng, T.-S., Kuo, Y.-L., Wu, A. T.-H., Tran, T.-H., et al. (2019). Identification of withaferin A as a potential candidate for anti-cancer therapy in non-small cell lung cancer. Cancers (Basel) 11, 1003. doi:10.3390/cancers11071003
Hussain, A., Dar, M. S., Bano, N., Hossain, M. M., Basit, R., Bhat, A. Q., et al. (2019). Identification of dinactin, a macrolide antibiotic, as a natural product-based small molecule targeting Wnt/β-catenin signaling pathway in cancer cells. Cancer Chemother. Pharmacol. 84, 551–559. doi:10.1007/s00280-019-03870-x
Isoherranen, N., Spiegelstein, O., Bialer, M., Zhang, J., Merriweather, M., Yagen, B., et al. (2003). Developmental outcome of levetiracetam, its major metabolite in humans, 2-pyrrolidinone N-butyric acid, and its enantiomer (R)-alpha-ethyl-oxo-pyrrolidine acetamide in a mouse model of teratogenicity. Epilepsia 44, 1280–1288. doi:10.1046/j.1528-1157.2003.21503.x
Jackson, M. J., and Turkington, D. (2005). Depression and anxiety in epilepsy. J. Neurol. Neurosurg. Psychiatry 76, i45–i47. doi:10.1136/jnnp.2004.060467
Jayaprakasam, B., Padmanabhan, K., and Nair, M. G. (2010). Withanamides in Withania somnifera fruit protect PC-12 cells from beta-amyloid responsible for Alzheimer’s disease. Phytother. Res. 24, 859–863. doi:10.1002/ptr.3033
Kanak, M. A., Shahbazov, R., Yoshimatsu, G., Levy, M. F., Lawrence, M. C., and Naziruddin, B. (2017). A small molecule inhibitor of NFκB blocks ER stress and the NLRP3 inflammasome and prevents progression of pancreatitis. J. Gastroenterol. 52, 352–365. doi:10.1007/s00535-016-1238-5
Kashyap, V. K., Dhasmana, A., Yallapu, M. M., Chauhan, S. C., and Jaggi, M. (2020). Withania somnifera as a potential future drug molecule for COVID-19. Future Drug Discov. 2, FDD50. doi:10.4155/fdd-2020-0024
Kataria, H., Kumar, S., Chaudhary, H., and Kaur, G. (2016). Withania somnifera suppresses tumor growth of intracranial allograft of glioma cells. Mol. Neurobiol. 53, 4143–4158. doi:10.1007/s12035-015-9320-1
Kataria, H., Wadhwa, R., Kaul, S. C., and 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
Khalil, M. I., Ahmmed, I., Ahmed, R., Tanvir, E. M., Afroz, R., Paul, S., et al. (2015). Amelioration of isoproterenol-induced oxidative damage in rat myocardium by Withania somnifera leaf extract. Biomed. Res. Int. 2015, 624159. doi:10.1155/2015/624159
Kim, G., Kim, T.-H., Hwang, E.-H., Chang, K.-T., Hong, J. J., and Park, J.-H. (2017). Withaferin A inhibits the proliferation of gastric cancer cells by inducing G2/M cell cycle arrest and apoptosis. Oncol. Lett. 14, 416–422. doi:10.3892/ol.2017.6169
Kim, S.-H., and Singh, S. V. (2014). Mammary cancer chemoprevention by withaferin A is accompanied by in vivo suppression of self-renewal of cancer stem cells. Cancer Prev. Res. 7, 738–747. doi:10.1158/1940-6207.CAPR-13-0445
Ku, S.-K., Han, M.-S., and Bae, J.-S. (2014). Withaferin A is an inhibitor of endothelial protein C receptor shedding in vitro and in vivo. Food Chem. Toxicol. 68, 23–29. doi:10.1016/j.fct.2014.03.009
Kulkarni, S. K., Akula, K. K., and 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. Available at: http://www.ncbi.nlm.nih.gov/pubmed/18697606.
Kumar, P., and Kumar, A. (2009). Possible neuroprotective effect of Withania somnifera root extract against 3-nitropropionic acid-induced behavioral, biochemical, and mitochondrial dysfunction in an animal model of Huntington’s disease. J. Med. Food 12, 591–600. doi:10.1089/jmf.2008.0028
Kumar, S., Seal, C. J., Howes, M. J. R., Kite, G. C., and Okello, E. J. (2010a). In vitro protective effects of Withania somnifera (L.) dunal root extract against hydrogen peroxide and β-amyloid(1-42)-induced cytotoxicity in differentiated PC12 cells. Phytother. Res. 24, 1567–1574. doi:10.1002/ptr.3261
Kumar, S., Seal, C. J., Howes, M. J. R., Kite, G. C., and Okello, E. J. (2010b). In vitro protective effects of Withania somnifera (L.) dunal root extract against hydrogen peroxide and β-amyloid(1-42)-induced cytotoxicity in differentiated PC12 cells. Phytother. Res. 24, 1567–1574. doi:10.1002/ptr.3261
Kurapati, K. R. V., Atluri, V. S. R., Samikkannu, T., and Nair, M. P. N. (2013). Ashwagandha (Withania somnifera) reverses β-amyloid1-42 induced toxicity in human neuronal cells: Implications in HIV-associated neurocognitive disorders (HAND). PLoS One 8, e77624. doi:10.1371/journal.pone.0077624
Kurup, P. A. (1958). Antibiot. Chemother. (Northfield, ill.) 8, 511–515. Available at: http://www.ncbi.nlm.nih.gov/pubmed/24544974.The antibacterial principle of Withania somnifera. I. Isoation and antibacterial activity
Kyakulaga, A. H., Aqil, F., Munagala, R., and Gupta, R. C. (2018). Withaferin A inhibits epithelial to mesenchymal transition in non-small cell lung cancer cells. Sci. Rep. 8, 15737. doi:10.1038/s41598-018-34018-1
Lee, J., Hahm, E.-R., and Singh, S. V. (2010). Withaferin A inhibits activation of signal transducer and activator of transcription 3 in human breast cancer cells. Carcinogenesis 31, 1991–1998. doi:10.1093/carcin/bgq175
Li, X., Zhu, F., Jiang, J., Sun, C., Wang, X., Shen, M., et al. (2015). Synergistic antitumor activity of withaferin A combined with oxaliplatin triggers reactive oxygen species-mediated inactivation of the PI3K/AKT pathway in human pancreatic cancer cells. Cancer Lett. 357, 219–230. doi:10.1016/j.canlet.2014.11.026
Lin, Y., Liu, H., Waraky, A., Haglund, F., Agarwal, P., Jernberg-Wiklund, H., et al. (2017). SUMO-modified insulin-like growth factor 1 receptor (IGF-1R) increases cell cycle progression and cell proliferation. J. Cell. Physiol. 232, 2722–2730. doi:10.1002/jcp.25818
Liu, X., Li, Y., Ma, Q., Wang, Y., and Song, A. L. (2019). Withaferin-A inhibits growth of drug-resistant breast carcinoma by inducing apoptosis and autophagy, endogenous reactive oxygen species (ROS) production, and inhibition of cell migration and nuclear factor kappa B (Nf-κB)/Mammalian target of rapamycin (m-TOR) signalling pathway. Med. Sci. Monit. 25, 6855–6863. doi:10.12659/MSM.916931
Malhotra, C. L., Das, P. K., and Dhalla, N. S. (1960). Studies on Withania ashwagandha. (Part I): Effect of total extract on central nervous system and smooth muscles. Indian J. Physiol. Pharmacol. 4, 35–48. Available at: http://www.ncbi.nlm.nih.gov/pubmed/14420294.
Malik, F., Kumar, A., Bhushan, S., Mondhe, D. M., Pal, H. C., Sharma, R., et al. (2009). Immune modulation and apoptosis induction: Two sides of antitumoural activity of a standardised herbal formulation of Withania somnifera. Eur. J. Cancer 45, 1494–1509. doi:10.1016/j.ejca.2009.01.034
Mallipeddi, H., Thyagarajan, A., and Sahu, R. P. (2021). Implications of Withaferin-A for triple-negative breast cancer chemoprevention. Biomed. Pharmacother. 134, 111124. doi:10.1016/j.biopha.2020.111124
Mathur, P., Sathishkumar, K., Chaturvedi, M., Das, P., Sudarshan, K. L., Santhappan, S., et al. (2020). Cancer statistics, 2020: Report from national cancer registry programme, India. JCO Glob. Oncol. 6, 1063–1075. doi:10.1200/GO.20.00122
Mathur, R., Gupta, S. K., Singh, N., Mathur, S., Kochupillai, V., and Velpandian, T. (2006). Evaluation of the effect of Withania somnifera root extracts on cell cycle and angiogenesis. J. Ethnopharmacol. 105, 336–341. doi:10.1016/j.jep.2005.11.020
Maxwell, S. R. J. (1995). Prospects for the use of antioxidant therapies. Drugs 49, 345–361. doi:10.2165/00003495-199549030-00003
Mayola, E., Gallerne, C., Esposti, D. D., Martel, C., Pervaiz, S., Larue, L., et al. (2011). Withaferin A induces apoptosis in human melanoma cells through generation of reactive oxygen species and down-regulation of Bcl-2. Apoptosis 16, 1014–1027. doi:10.1007/s10495-011-0625-x
Mazzoni, P., Shabbott, B., and Cortés, J. C. (2012). Motor control abnormalities in Parkinson’s disease. Cold Spring Harb. Perspect. Med. 2, a009282. doi:10.1101/cshperspect.a009282
Mirjalili, M. H., Moyano, E., Bonfill, M., Cusido, R. M., and Palazón, J. (2009a). Steroidal lactones from Withania somnifera, an ancient plant for novel medicine. Molecules 14, 2373–2393. doi:10.3390/molecules14072373
Mirjalili, M., Moyano, E., Bonfill, M., Cusido, R., and Palazón, J. (2009b). Steroidal lactones from Withania somnifera, an ancient plant for novel medicine. Molecules 14, 2373–2393. doi:10.3390/molecules14072373
Mishra, L. C., Singh, B. B., and Dagenais, S. (2000). Scientific basis for the therapeutic use of Withania somnifera (ashwagandha): A review. Altern. Med. Rev. 5, 334–346. Available at: http://www.ncbi.nlm.nih.gov/pubmed/10956379.
Munagala, R., Kausar, H., Munjal, C., and Gupta, R. C. (2011). Withaferin A induces p53-dependent apoptosis by repression of HPV oncogenes and upregulation of tumor suppressor proteins in human cervical cancer cells. Carcinogenesis 32, 1697–1705. doi:10.1093/carcin/bgr192
Nagalingam, A., Kuppusamy, P., Singh, S. V., Sharma, D., and Saxena, N. K. (2014). Mechanistic elucidation of the antitumor properties of withaferin A in breast cancer. Cancer Res. 74, 2617–2629. doi:10.1158/0008-5472.CAN-13-2081
Najar, R. A., Wani, N. A., Bhat, J. A., Dar, N. J., Rahat, B., Gupta, A. P., et al. (2018). Modulation of dietary folate with age confers selective hepatocellular epigenetic imprints through DNA methylation. J. Nutr. Biochem. 53, 121–132. doi:10.1016/j.jnutbio.2017.10.007
Nalli, Y., Dar, M. S., Bano, N., Rasool, J. U., Sarkar, A. R., Banday, J., et al. (2019). Analyzing the role of cannabinoids as modulators of Wnt/β-catenin signaling pathway for their use in the management of neuropathic pain. Bioorg. Med. Chem. Lett. 29, 1043–1046. doi:10.1016/j.bmcl.2019.03.013
Nishikawa, Y., Okuzaki, D., Fukushima, K., Mukai, S., Ohno, S., Ozaki, Y., et al. (2015). Withaferin A induces cell death selectively in androgen-independent prostate cancer cells but not in normal fibroblast cells. PLoS One 10, e0134137. doi:10.1371/journal.pone.0134137
Nitti, M., Piras, S., Brondolo, L., Marinari, U. M., Pronzato, M. A., and Furfaro, A. L. (2018). Heme oxygenase 1 in the nervous system: Does it favor neuronal cell survival or induce neurodegeneration? Int. J. Mol. Sci. 19, 2260. doi:10.3390/ijms19082260
Okamoto, S., Tsujioka, T., Suemori, S.-I., Kida, J.-I., Kondo, T., Tohyama, Y., et al. (2016). Withaferin A suppresses the growth of myelodysplasia and leukemia cell lines by inhibiting cell cycle progression. Cancer Sci. 107, 1302–1314. doi:10.1111/cas.12988
Paul, S., Chakraborty, S., Anand, U., Dey, S., Nandy, S., Ghorai, M., et al. (2021). Withania somnifera (L.) dunal (ashwagandha): A comprehensive review on ethnopharmacology, pharmacotherapeutics, biomedicinal and toxicological aspects. Biomed. Pharmacother. 143, 112175. doi:10.1016/j.biopha.2021.112175
Pingali, U., Pilli, R., and Fatima, N. (2014). Effect of standardized aqueous extract of Withania somnifera on tests of cognitive and psychomotor performance in healthy human participants. Pharmacogn. Res. 6, 12–18. doi:10.4103/0974-8490.122912
Prakash, J., Chouhan, S., Yadav, S. K., Westfall, S., Rai, S. N., and Singh, S. P. (2014). Withania somnifera alleviates parkinsonian phenotypes by inhibiting apoptotic pathways in dopaminergic neurons. Neurochem. Res. 39, 2527–2536. doi:10.1007/s11064-014-1443-7
Qadir Bhat, A., Owais Ayaz, M., Hussain, R., Dar, M. S., Hossain, M. M., Showket, F., et al. (2022). Identification of a stretch of four discontinuous amino acids involved in regulating kinase activity of IGF1R. J. Cell Sci. 135, jcs260014. doi:10.1242/jcs.260014
Raghavan, A., and Shah, Z. A. (2015). Withania somnifera improves ischemic stroke outcomes by attenuating PARP1-AIF-mediated caspase-independent apoptosis. Mol. Neurobiol. 52, 1093–1105. doi:10.1007/s12035-014-8907-2
RajaSankar, S., Manivasagam, T., Sankar, V., Prakash, S., Muthusamy, R., Krishnamurti, A., et al. (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
Rasheed, A., Satyanarayana, K. V., Gulabi, P. S., and Rao, M. S. (2013). Chemical and pharmacological standardization of ashwagandhadi lehyam: An ayurvedic formulation. J. Complement. Integr. Med. 10, 1–9. doi:10.1515/jcim-2012-0026
Rivera, D., Allkin, R., Obón, C., Alcaraz, F., Verpoorte, R., and Heinrich, M. (2014). What is in a name? The need for accurate scientific nomenclature for plants. J. Ethnopharmacol. 152, 393–402. doi:10.1016/j.jep.2013.12.022
Saggam, A., Tillu, G., Dixit, S., Chavan-Gautam, P., Borse, S., Joshi, K., et al. (2020). Withania somnifera (L.) dunal: A potential therapeutic adjuvant in cancer. J. Ethnopharmacol. 255, 112759. doi:10.1016/j.jep.2020.112759
Sahni, Y. P., and Srivastava, D. N. (1993). Anti-inflammatory activity of Withania somnifera: Possible mode of action. J. Appl. Anim. Res. 3, 129–136. doi:10.1080/09712119.1993.9705964
Saleem, S., Muhammad, G., Hussain, M. A., Altaf, M., and Bukhari, S. N. A. (2020). Withania somnifera L.: Insights into the phytochemical profile, therapeutic potential, clinical trials, and future prospective. Iran. J. Basic Med. Sci. 23, 1501–1526. doi:10.22038/IJBMS.2020.44254.10378
Sehgal, N., Gupta, A., Valli, R. K., Joshi, S. D., Mills, J. T., Hamel, E., et al. (2012). Withania somnifera reverses Alzheimer’s disease pathology by enhancing low-density lipoprotein receptor-related protein in liver. Proc. Natl. Acad. Sci. U. S. A. 109, 3510–3515. doi:10.1073/pnas.1112209109
Serrano-Pozo, A., Frosch, M. P., Masliah, E., and Hyman, B. T. (2011). Neuropathological alterations in Alzheimer disease. Cold Spring Harb. Perspect. Med. 1, a006189. doi:10.1101/cshperspect.a006189
Sharma, M., Gaur, A., Vishwakarma, P., Goel, R. K., and Saxena, K. K. (2021). Evaluation of hepatoprotective potential of aqueous extract of Withania somnifera in albino rats. Int. J. Basic Clin. Pharmacol. 10, 255. doi:10.18203/2319-2003.ijbcp20210477
Sharma, S., Ahmad, M., Bhat, J. A., Kumar, A., Kumar, M., Zargar, M. A., et al. (2014). Design, synthesis and biological evaluation of β-boswellic acid based HDAC inhibitors as inducers of cancer cell death. Bioorg. Med. Chem. Lett. 24, 4729–4734. doi:10.1016/j.bmcl.2014.08.007
Shohat, B., Gitter, S., Abraham, A., and Lavie, D. (1967). Antitumor activity of withaferin A (NSC-101088). Cancer Chemother. Rep. 51, 271–276. Available at: http://www.ncbi.nlm.nih.gov/pubmed/6062297.
Singh, N., Bhalla, M., de Jager, P., and Gilca, M. (2011). An overview on ashwagandha: A rasayana (rejuvenator) of Ayurveda. Afr. J. Tradit. Complement. Altern. Med. 8, 208–213. doi:10.4314/ajtcam.v8i5S.9
Singh, N., Yadav, S. S., Rao, A. S., Nandal, A., Kumar, S., Ganaie, S. A., et al. (2021). Review on anticancerous therapeutic potential of Withania somnifera (L.) Dunal. J. Ethnopharmacol. 270, 113704. doi:10.1016/j.jep.2020.113704
Srinivasan, S., Ranga, R. S., Burikhanov, R., Han, S.-S., and Chendil, D. (2007). Par-4-Dependent apoptosis by the dietary compound withaferin A in prostate cancer cells. Cancer Res. 67, 246–253. doi:10.1158/0008-5472.CAN-06-2430
Stan, S. D., Hahm, E.-R., Warin, R., and Singh, S. V. (2008b). Withaferin A causes FOXO3a- and Bim-dependent apoptosis and inhibits growth of human breast cancer cells in vivo. Cancer Res. 68, 7661–7669. doi:10.1158/0008-5472.CAN-08-1510
Stan, S. D., Hahm, E.-R., Warin, R., and Singh, S. V. (2008a). Withaferin A causes FOXO3a- and bim-dependent apoptosis and inhibits growth of human breast cancer cells in vivo. Cancer Res. 68, 7661–7669. doi:10.1158/0008-5472.CAN-08-1510
Strooper, De, Vassar, R., and Golde, T. (2010). The secretases: Enzymes with therapeutic potential in alzheimer disease. Nat. Rev. Neurol. 6, 99–107. doi:10.1038/nrneurol.2009.218
Suman, S., Das, T. P., Moselhy, J., Pal, D., Kolluru, V., Alatassi, H., et al. (2016). Oral administration of withaferin A inhibits carcinogenesis of prostate in TRAMP model. Oncotarget 7, 53751–53761. doi:10.18632/oncotarget.10733
Sung, H., Ferlay, J., Siegel, R. L., Laversanne, M., Soerjomataram, I., Jemal, A., et al. (2021). Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. Ca. Cancer J. Clin. 71, 209–249. doi:10.3322/caac.21660
Surya, U. R., Naik, P. M., Vinayak, U., and Praveen, N. (2021). A critical review of anticancer properties of Withania somnifera (L.) Dunal with respect to the biochemical mechanisms of its phytochemical constituents. Plant Sci. Today 8, 236–249. doi:10.14719/pst.2021.8.2.969
Tanna, I. R., Aghera, H. B., Ashok, B. K., and Chandola, H. M. (2012). Protective role of Ashwagandharishta and flax seed oil against maximal electroshock induced seizures in albino rats. Ayu 33, 114–118. doi:10.4103/0974-8520.100327
Tiwari, S., Atluri, V. S. R., Yndart Arias, A., Jayant, R. D., Kaushik, A., Geiger, J., et al. (2018). Withaferin A suppresses beta amyloid in app expressing cells: Studies for tat and cocaine associated neurological dysfunctions. Front. Aging Neurosci. 10, 291. doi:10.3389/fnagi.2018.00291
Udayakumar, R., Kasthurirengan, S., Mariashibu, T. S., Rajesh, M., Anbazhagan, V. R., Kim, S. C., et al. (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
Uddin, M. S., Al Mamun, A., Kabir, M. T., Jakaria, M., Mathew, B., Barreto, G. E., et al. (2019). Nootropic and anti-alzheimer’s actions of medicinal plants: Molecular insight into therapeutic potential to alleviate Alzheimer’s neuropathology. Mol. Neurobiol. 56, 4925–4944. doi:10.1007/s12035-018-1420-2
Um, H. J., Min, K., Kim, D. E., and Kwon, T. K. (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
Upadhyay, B. N., and Gupta, V. (2011). A clinical study on the effect of rishyagandha (Withania coagulans) in the management of prameha (type II diabetes mellitus). Ayu 32, 507–511. doi:10.4103/0974-8520.96124
Vareed, S. K., Bauer, A. K., Nair, K. M., Liu, Y., Jayaprakasam, B., and Nair, M. G. (2014). Blood-brain barrier permeability of bioactive Withanamides present in Withania somnifera fruit extract. Phytother. Res. 28, 1260–1264. doi:10.1002/ptr.5118
Wadhwa, R., Singh, R., Gao, R., Shah, N., Widodo, N., Nakamoto, T., et al. (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
Widodo, N., Kaur, K., Shrestha, B. G., Takagi, Y., Ishii, T., Wadhwa, R., et al. (2007). Selective killing of cancer cells by leaf extract of ashwagandha: Identification of a tumor-inhibitory factor and the first molecular insights to its effect. Clin. Cancer Res. 13, 2298–2306. doi:10.1158/1078-0432.CCR-06-0948
Wongtrakul, J., Thongtan, T., Kumrapich, B., Saisawang, C., and Ketterman, A. J. (2021). Phytochemical andrographolide modulates NF-κB and JNK in human neuroblastoma SH-SY5Y cells, a cell model for Parkinson's disease. Heliyon 7, e04121. doi:10.1016/j.heliyon.2020.e04121
Yu, Y., Hamza, A., Zhang, T., Gu, M., Zou, P., Newman, B., et al. (2010a). Withaferin A targets heat shock protein 90 in pancreatic cancer cells. Biochem. Pharmacol. 79, 542–551. doi:10.1016/j.bcp.2009.09.017
Keywords: cancer, neurodegenerative disorders, Alzheimer’s disease, Withania somnifera, stroke
Citation: Bhat JA, Akther T, Najar RA, Rasool F and Hamid A (2022) Withania somnifera (L.) Dunal (Ashwagandha); current understanding and future prospect as a potential drug candidate. Front. Pharmacol. 13:1029123. doi: 10.3389/fphar.2022.1029123
Received: 26 August 2022; Accepted: 30 November 2022;
Published: 12 December 2022.
Edited by:
Shahnawaz A. Bhat, Aligarh Muslim University, IndiaReviewed by:
Mumtaz Anwar, University of Illinois at Chicago, United StatesSamirul Bashir, University of Massachusetts Medical School, United States
Copyright © 2022 Bhat, Akther, Najar, Rasool and Hamid. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Javeed Ahmad Bhat, javeedbhat3@gmail.com; Abid Hamid, abidhamid@cukashmir.ac.in
†These authors have contributed equally to this work