A Comprehensive Review for Drug Target on

Terminalia arjuna (Roxb.): Ethnopharmacological, Phytochemical, Pharmacognostical, and Clinical Significance

 

Pooja Singh1, Divya Sharma1, Akanksha Singh1, Arjun Singh2*

1Department of Pharmacology, School of Pharmaceutical Sciences,

Bhagwant University, Sikar Road, Ajmer, Rajasthan 305004, India.

2Department of Medicine, Sidney Kimmel Medical College,

Thomas Jefferson University, Philadelphia, PA 19107, United States.

*Corresponding Author E-mail: arjunphar@gmail.com

 

ABSTRACT:

Popular medicinal plant Tinospora cordifolia is used in numerous traditional medicines to treat a wide range of illnesses. The common names Amrita and Guduchi are members of the Menispermaceae family. It has been used to treat a variety of illnesses, including diabetes, leprosy, skin conditions, dysentery, and fever, and is regarded as an essential herbal plant in the Indian system of medicine (ISM). Alkaloids, Terpenoids, Lignans, Steroids, and other chemical compounds have been reported to be present in the plant, establishing the phytochemistry and pharmacological activity of Tinospora cordifolia. The current review emphasizes the importance of pharmacology, specifically antioxidant activity, antimicrobial activity, antibacterial activity, antifungal activity, anti-diabetic activity, antistress activity, hypolipidemic effect, hepatic disorder, anticancer anti-HIV potential, antiosteoporotic effects, antitoxic effects, wound healing, anticomplementary activity. In this review, the pharmacological importance of antioxidant activity, antimicrobial activity, antibacterial activity, antifungal activity, anti-diabetic activity, anti-stress activity, hypolipidemic effect, hepatic disorder, anticancer anti-HIV potential, antiosteoporotic effects, antitoxic effects, wound healing, anticomplementary activity, and immunomodulating activity, systemic infection, and Parkinson's disease is highlighted.

 

KEYWORDS: Tinospora cordifolia, Alkaloids, Terpenoids, Lignans, phytochemicals, Medicinal plants.

 

 


INTRODUCTION:

T. cordifolia is also known as Guduchi/Amrita and by the Latin names Tinospora cordifolia (Wild) Hook. F. & Thomson, TinosporaGulancha/Indian Tinospora, and Giloya1. Its scientific name is Tinospora sinensis (Lour.) Merr. It can be found in Myanmar, Sri Lanka, and China and is a member of the Menispermaceae family2. The plant is frequently used as conventional ayurvedic medicine and possesses a number of therapeutic benefits including the treatment of jaundice, rheumatism, urinary disorders, skin diseases, diabetes, anemia, inflammation,

 

 

allergic conditions, anti-periodic properties, and radioprotective effects, among other conditions. To treat bowel obstruction and as a powerful emetic, Giloya (T. cordifolia) root is used3-5.

 

The starch from this plant relieves burning, boosts energy, and stimulates the appetite. It also serves as a useful home remedy for chronic fever. In addition to helping the immune system and the body's resistance to infections, giloya is effective in the treatment of helminthiasis, heart conditions, leprosy, rheumatoid arthritis, and other conditions6-9. It also supports normal white blood cell structure, function, and levels. Additionally, it aids in the treatment of digestive disorders like hepatitis and liver diseases like hyperacidity, colitis, worm infestations, loss of appetite, abdominal pain, excessive thirst, and vomiting10-12. The chemical components of the plant, which include diterpenoid lactones, glycosides, steroids, sesquiterpenoids, phenolic compounds, essential oils, a combination of fatty acids, and polysaccharides, are what give rise to the plant's pharmacological effects. These chemical constituents are also found in the root, stem, and entire body of the plant13-15.

 

It is a sizable, deciduous climbing shrub that spreads widely and has several coiled branches with various morphologies16. The plant's filiform, fleshy, and climbing stem has bark that ranges in color from white to gray. The stem's powder is creamish brown or dark brown, has a distinctive odor and bitter taste, and is used to treat fever, urinary diseases, and dyspepsia. The "Guduchi-satva" starch derived from the stem. It is very nutritious and aids in digestion17. This plant has round, pulvinate, heart-shaped, simple, alternate, long-petioled (15 cm), partially twisted, and halfway around leaves. Oval, 10–20 cm long, seven nerved, deeply cordate at the base, and membranous describe the lamina18. Flowers are axillary, unisexual, and have 2–9cm-long leaflet branches that are greenish yellow in color19.

 

METHODS:

Materials:

The available information on various plants based traditionally used for pharmacological, ethnomedicinal, phytochemical and treatment of disorders was collected through electronic databases searches using PubMed, Scopus, Science Direct, Google Scholar, and Web of Science, as well as a library search for articles published in peer-reviewed journal articles in this review survey20.

 

The chemical components of T. cordifolia include alkaloids, glycosides, steroids, phenolics, aliphatic compounds, and polysaccharide21. The leaves also contain high levels of calcium, phosphorus, and protein (11.2%), among other nutrients. The structure of the stem, which is determined by various spectroscopic studies23,24,25, has been established. The stem contains clerodane furono diterpene glucoside (amritoside A, B, C, and D). While the structure of the active chemical component for Tinospora cordifolia has been shown in Figure, some of the essential constituents reported in table and major constituents22-25.

The extract demonstrates the anticancer potential in a mouse skin cancer model induced by 7,12-dimethylbenz (a) anthracene (DMBA). A significant rise in the levels of gamma-glutamyl transferase, aspartate transaminase, alanine transaminase, triglyceride, cholesterol, HDL, and LDL (P 0.05) in alcoholic sample was reported, whereas their level got downregulated after TCE intervention, patients showed the normalized liver function of T. cordifolia stand to relieve the symptoms26-28.

 

A response surface methodology to examine the anticancer properties of T. cordifolia palmatine extract in animal models (RSM). The extract demonstrates the anticancer potential in a mouse skin cancer model induced by 7,12-dimethylbenz(a)anthracene (DMBA). A prepared the extract in a dose-dependent manner at concentrations of 200, 400, and 600mg/kg dry weight. 750 mg/kg body weight of a 50% methanolic extract of cordifolia was administered for 30 days to C57 BI mice. the tumor size shortens life29-35.

 

Terminalia arjuna (Roxb.) Wight &Arn. (T. arjuna):

Terminalia arjuna (Roxb.) Wight &Arn. (T. arjuna) is one of the most accepted and beneficial medicinal plants in indigenous system of medicine for the treatment of various critical diseases. Terminalia arjuna, sometimes known as arjuna, is a member of the Combretaceae family. Its bark decoction is used for anginal discomfort, hypertension, congestive heart failure, and dyslipidaemia on the Indian subcontinent, based on centuries of observations by ancient physicians. Arjuna's potential for treating a variety of cardiovascular illnesses needs to be investigated further. It is belonging to genus Terminalia. The major pharmacological activities are analgesic, antiaggregant, antidote, anti-ischemic, antispasmodic, aphrodisiac, astringent, bradycardic, cardioprotective, deobstruent, diuretic, expectorant, hemostat, hepatoprotective, hypertensive, hypotensive, laxative, litholytic, positive inotropic, prostaglandigenic, sedative, tonic. T. arjuna's principal ingredients in stem bark, root bark, fruits, leaves, and seeds have all been identified. The main ingredients of T. arjuna include polyphenols, flavonoids, tannins, triterpenoids, saponins, sterols, and minerals. T. arjuna also contains tryptophan, tyrosine, histidine, and cysteine, among other amino acids25-35.


 

The major phytochemical constituents are found in different part of arjuna

Active Component

Compounds

Terpenoids

Tinosporide, Furanolactone diterpene, Furanolactone clerodane diterpene, furanoid diterpene, Tinosporaside, ecdysteronemakisterone and several glucosides isolated as poly acetate, phenylpropene disaccharides cordifolioside A, B and C, cordifoliside D and E, Tinocordioside, cordioside, palmatosides C and F, Sesquiterpene glucoside tinocordifolioside, Sesquiterpene tinocordifolin.

Alkaloids

Tinosporine, (S), Magnoflorine, (S), Berberine, (S), Choline, (S), Jatrorrhizine, (S), 1,2-Substituted pyrrolidine(S), Alkaloids, viz. jatrorrhizine, palmatine, beberine, tembeterine, choline.

Lignans

3 (a, 4-dihydroxy-3-methoxybenzyl)-4-(4-hydroxy-3-methoxybenzyl), (S)

Steroids

Giloinsterol, (S), ß-Sitosterol, (S), 20a- Hydroxy ecdysone, (S).

Others

Giloin, Tinosporan acetate, Tinosporal acetate, Tinosporidine, Heptacosanol, Octacosanol, sinapic acid, Tinosponone, two phytoecdysones, an immunologically active arabinogalactan.

 


Stem bark:

1.     Triterpenoids: Arjunin, Arjunic acid, Arjungenin, Terminic acid, Terminoltin, Arjunolic acid

2.     Ursane triterpenoids: 2α,3β-dihydroyurs-12,18-oic acid 28-O-β-d-glucopyranosyl ester, 2α,3β,23-trihydroxyurs-12,18-dien-28-oic acid 28-O-β-glucopyranosyl ester, Qudranoside VIII, Kajiichigoside F1, 2α,3β,23-trihydroxyurs-23-trihydroxyurs-12,19-dien-28-oic acid 28-O-β-d-glucopyranosyl ester

3.     Glycosides: Arjunetin, Arjunoside I, II, Arjunolone, Arjunolitin, Arjunaphthanoloside, Arjunglucoside IV and V, Arjunasides A-E,      Olean-3β, 22β-diol-12-en-28 β-D-glucopyranosie-oic acid, Terminarjunoside I and II, Terminoside A, Termionic acid         

4.     Flavonoids and phenolics: Arjunone, Luteolin, Baicalein, Ethyl gallate, Gallic acid, Kempferol, Oligomeric proanthocyanidins, Pelargonidin, Quercetin, (+)-catechin, (+)-gallocatechin and (−)-epigallocatechin, Gallic acid, ellagic acid and its derivatives such as 3-O-methyl-ellagic acid 4-O-β-d-xylopyranoside, 3-O-methyl ellagic acid 3-O-rhamnoside,  3-O-methyl ellagic acid 4′-O-α-l-rhamnophranoside(−)-epicatechin            

5.     Tannins: Pyrocatechols, Punicallin, Castalagin, Casuariin, Casuarinin, Punicalagin, Terchebulin, Terflavin C

6.     Minerals and trace elements:Calcium, magnesium, aluminum, zinc, copper, silica    

7.     Other compounds: β-Sitosterol

 

Roots:

1.     Triterpenoids: Arjunoside I-IV, Arjunolic acid, Oleanolic acid, Terminic acid, 2α,19α-Dihydroxy-3Oxo-Olean-12-En28-Olic acid 28-O-β-d-glucopyranoside, Arjunic acid        

2.     Glycosides: Arjunetosie (3-O-β-d-glucopyranosyl-2α, 3β, 19α-trihydroxyolean-12-en-28-oic acid 28-O-β-d-glucopyranoside)         

 

Fruits:

1.     Triterpenoids and flavonoids: Arjunic acid, Arjunone, Arachidic stearate, Cerasidin, Ellagic acid, Fridelin, Gallic acid, Hentriacontane, Methyl oleaolate, Myristyl oleate, β-Sitisterol 

 

Leaves and seeds:

1.     Flavonoids and glycosides: Luteolin, 14,16-dianhydrogitoxigenin 3-β-d-xylopyranosyl-(1 > 2)-O-β-d-galactopyranoside

 

CONCLUSION:

T. cordifolia is a medicinal plant that contains a wide range of substances. Alkaloids, steroids, glycosides, sesquiterpenoids, and other bioactive substances have all been discussed. The artistic antifungal, antioxidant, antimicrobial, antibacterial, hypolipidemic, hepatic disorder, anticancer, anti-HIV potential, antiosteoporotic, antitoxic, wound healing, anticomplementary, immunomodulating, systemic infection, and Parkinson's disease properties of T. cordifolia are highlighted in the current review. Since the beginning of Ayurvedic medicine, it has been successfully used, and its products are used for both their better financial and therapeutic utilization. In this regard, more research must be done to examine T. cordifolia's potential in the prevention and treatment of diseases. This review can be applied clinically and for additional research purposes in the novel drug discovery.

 

CONFLICT OF INTEREST:

The author has no conflicts of interest.

 

ACKNOWLEDGMENTS:

The author would like to thank NCBI, PubMed and Web of Science for the free database services for their kind support during this study.

 

REFERENCES:

1.      World Health Organization. WHO traditional medicine strategy: 2014-2023. World Health Organization, 2013.

2.      World Health Organization. WHO global report on traditional and complementary medicine 2019. World Health Organization, 2019.

3.      Qi, Zhang. Who traditional medicine strategy. 2014-2023. Geneva: World Health Organization 188 (2013).

4.      World Health Organization. The regional strategy for traditional medicine in the Western Pacific (2011-2020). (2012).

5.      World Health Organization. Regional strategy for traditional medicine in the Western Pacific. Manila: WHO Regional Office for the Western Pacific, 2002.

6.      Kasilo, Ossy MJ, and Jean‐Baptiste Nikiema. World Health Organization perspective for traditional medicine. Novel Plant Bioresources: Applications in Food, Medicine and Cosmetics. 2014: 23-42.

7.      Zhang, Qi, Aditi Sharan, Stéphane Alexandre Espinosa, Daniel Gallego-Perez, and John Weeks. The path toward integration of traditional and complementary medicine into health systems globally: The World Health Organization report on the implementation of the 2014–2023 strategy. The Journal of Alternative and Complementary Medicine. 2019;  25(9): 869-871.

8.      Hajare, Ashok A, Sachin S Mali, Sonali S Gorde, Jyoti D Thorat, and Sachin S Salunkhe. Narrative Review: A Rational Approach to Needle Free Insulin Technology, 2014, 11.

9.      Lakshmi, K. Effectiveness of Nursing Care of Antenatal Mothers with Gestational Diabetes Mellitus. Asian Journal of Nursing Education and Research. 2020;  10(3); 286.

10.   Raju, Vidya, Jasmine Joy Bell, N. J. Merlin, and Shaiju S Dharan. Ethno Pharmacological Uses of Artocarpus Altilis -A Review. Asian Journal of Pharmaceutical Research. 2017; 7(4); 239.

11.   Somwanshi, Sachin B., Punam D. Bairagi, and Kiran B. Kotade. Study of Gestational Diabetes Mellitus: A Brief Review. Asian Journal of Pharmaceutical Research. 2017; 7(2): 118.

12.   Yousaf, Aqsa, and Sammia Shahid. The Study of Anethum Graveolens L. (Dill) in the Case of Diabetes Mellitus (DM). Asian Journal of Research in Pharmaceutical Science. 2020;  4(4): 248–56.

13.   Gautam, Y., Dwivedi, S., Srivastava, A., Hamidullah, Singh, A., Chanda, D., Singh, J., Rai, S., Konwar, R., Negi, A.S. 2-(3′,4′-Dimethoxybenzylidene)tetralone induces anti-breast cancer activity through microtubule stabilization and activation of reactive oxygen species. RSC Adv. 2016; 6: 33369–33379.

14.   Hamid, A.A., Hasanain, M., Singh, A., Bhukya, B., Omprakash, Vasudev, P.G., Sarkar, J., Chanda, D., Khan, F., Aiyelaagbe, O.O., Negi, A.S. Synthesis of novel anticancer agents through opening of spiroacetal ring of diosgenin. Steroids. 2014; 87: 108–118.

15.   Jain, S., Singh, A., Khare, P., Chanda, D., Mishra, D., Shanker, K., Karak, T. Toxicity assessment of Bacopa monnieri L. grown in biochar amended extremely acidic coal mine spoils. Ecological Engineering. 2017; 108: 211–219.

16.   Mishra, D., Jyotshna, Singh, A., Chanda, D., Shanker, K., Khare, P. Potential of di-aldehyde cellulose for sustained release of oxytetracycline: A pharmacokinetic study. International Journal of Biological Macromolecules. 2019; 136: 97–105.

17.   Sathish Kumar, B., Singh, Aastha, Kumar, A., Singh, J., Hasanain, M., Singh, Arjun, Masood, N., Yadav, D.K., Konwar, R., Mitra, K., Sarkar, J., Luqman, S., Pal, A., Khan, F., Chanda, D., Negi, A.S. Synthesis of neolignans as microtubule stabilisers. Bioorganic & Medicinal Chemistry. 2014; 22: 1342–1354.

18.   Singh, A., Mohanty, I., Singh, J., Rattan, S. BDNF augments rat internal anal sphincter smooth muscle tone via RhoA/ROCK signaling and nonadrenergic noncholinergic relaxation via increased NO release. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2020;318: G23–G33.

19.   Singh, A., Rattan, S. BDNF rescues aging-associated internal anal sphincter dysfunction. American Journal of Physiology-Gastrointestinal and Liver Physiology.2021; 321: G87–G97.

20.   Singh, A., Singh, J., Rattan, S. Evidence for the presence and release of BDNF in the neuronal and non‐neuronal structures of the internal anal sphincter. Neurogastroenterology and Motility. 2021.

21.   Manmohan, S., Arjun, S., Khan, S. P., Eram, S., and Sachan, N. K. Green chemistry potential for past, present and future perspectives. International Research Journal of Pharmacy. 2012; 3: 31-36.

22.   Singh, A., R. Sharma, K. M. Anand, S. P. Khan, and N. K. Sachan. "Food-drug interaction." International Journal of Pharmaceutical & Chemical Science 1, no. 1 (2012): 264-279.

23.   Thanh-Hoang, N.V., Loc, N., Nguyet, D., Thien-Ngan, N., Khang, T., Cao, H., Le, L. Plant Metabolite Databases: From Herbal Medicines to Modern Drug Discovery. J. Chem. Inf. Model. 2020; 60: 1101–1110.

24.   Kumar, S.; Malhotra, R.; Kumar, D. Euphorbia hirta: Its chemistry, traditional and medicinal uses, and pharmacological activities. Pharmacogn. Rev. 2010; 4: 58–61.

25.   AK Meena, MM Rao, RP Meena, P Panda, Renu. Pharmacological and Phytochemical Evidences for the Plants of Wedelia Genus– A Review. Asian J. Pharm. Res. 2011; 1(1):  7-12.

26.   M. Ezhumalai, G. Hemalatha, J.P. Poornima, K.V. Pugalendi. Inhibition of Lactobacillus growth by amino acids and phytochemicals in the fermentation of curd by disc diffusion method. Asian J. Pharm. Res. 2013;  3(4): 189-193.

27.   An Aqueous Extract of the Leaves of Chromolaena odorata Moderated Plasma Biochemical and Hematological Indices of Sub-Chronic Salt-Loaded Rats. Asian J. Pharm. Res. 2014; 4(1): 24-35.

28.   N. S. Patil, K. B. Patil, M. R. Patil, R. A. Ahirrao. Antimitotic Activity of Fruits of Momordica dioica by using Allium cepa Root Tip Assay. Asian J. Pharm. Res. 2018; 8(4): 221-224.

29.   Arjun Singh. A Review of various aspects of the Ethnopharmacological, Phytochemical, Pharmacognostical, and Clinical significance of selected Medicinal plants. Asian Journal of Pharmacy and Technology. 2022; 12(4): 349-0. doi: 10.52711/2231-5713.2022.00055

30.   Devender Paswan, Urmila Pande, Alka Singh, Divya Sharma, Shivani Kumar, Arjun Singh. Epidemiology, Genomic Organization, and Life Cycle of SARS CoV-2. Asian Journal of Nursing Education and Research. 2023; 13(2):141-4.

31.   Arjun Singh, Rupendra Kumar, Sachin Sharma. Natural products and Hypertension: Scope and role in Antihypertensive Therapy. Asian Journal of Nursing Education and Research. 2023; 13(2): 162-6.

32.   Arjun Singh. A Review of various aspects of the Ethnopharmacological, Phytochemical, Pharmacognostical, and Clinical significance of selected Medicinal plants. Asian Journal of Pharmacy and Technology. 2012; 4(4):349-0.

33.   Arjun Singh, Rupendra Kumar. An Overview on Ethnopharmacological, Phytochemical, and Clinical Significance of Selected Dietary Polyphenols. Asian Journal of Research in Chemistry. 2023; 16(1):8-2.

34.   Arjun Singh. Plant-based Isoquinoline Alkaloids: A Chemical and Pharmacological Profile of Some Important Leads. Asian Journal of Research in Chemistry. 2023; 16(1):43-8.

35.   Singh, A., Chanda, D., and Negi, A. S. Antihypertensive activity of Diethyl-4, 4'-dihydroxy-8, 3'-neolign-7, 7'-dien-9, 9'-dionate through increase in intracellular cGMP level and blockade of calcium channels (VDCC) and opening of potassium channel and in vivo models (SHRs and L-NAME induced hypertension). In Proceedings for Annual Meeting of The Japanese Pharmacological Society WCP2018 (The 18th World Congress of Basic and Clinical Pharmacology) (pp. PO1-2). Japanese Pharmacological Society. 2018.

 

 

 

 

 

 

 

 

 

Received on 29.12.2022                    Modified on 22.04.2023

Accepted on 26.07.2023                   ©AJRC All right reserved

Asian J. Research Chem. 2023; 16(6):448-452.

DOI: 10.52711/0974-4150.2023.00074