A Comprehensive Review on Cytotoxic Potential of Atropa acuminata

Authors

  • Arnab Bhowmick Himalayan Pharmacy Institute, Majhitar, Sikkim-737136
  • Sandip Mondal Department of Pharmacognosy, Himalayan Pharmacy Institute, Majitar, Sikkim, 737136, India
  • Ritika Roy Department of Pharmacognosy, Himalayan Pharmacy Institute, Majitar, Sikkim, 737136, India
  • Rajat Das Department of Pharmacognosy, Himalayan Pharmacy Institute, Majitar, Sikkim, 737136, India
  • Jyochhana Priya Mohanty Department of Pharmacognosy, Himalayan Pharmacy Institute, Majitar, Sikkim, 737136, India

DOI:

https://doi.org/10.61114/UJPSR.10.1.2026.26-31

Keywords:

Atropa acuminata, cytotoxicity, tropane alkaloids, atropine, alkaloid extraction, acid-base extraction, phytochemical analysis, MTT assay, anticancer potential

Abstract

Atropa acuminata it contains various bioactive compounds, like particularly tropane alkaloids, it contributes to its therapeutic properties. Different alkaloids found within this plant include; atropine, hyoscyamine, and scopolamine demonstrating sedative, anti-spasmodic, and antidote properties. The therapeutic effects of the plant are further enhanced by the other classes of phytochemicals the plant contains, including flavonoids, tannins, saponins, anthraquinones, and phytosterols. Because of the plant's extensive class of phytochemicals and long history of traditional use, scientific research has looked into a variety of impacts of the plant. The phytochemical components of plants have been the subject of extensive scientific research about their anticancer properties. Information for this study was acquired from many credible scholarly sources. All sources of information were employed to identify the technique in which atropine can be produced from dried leaf and root elements of the plant.The study also examined several extraction methods for pharmaceuticals, the effects of induced mutagenesis via sodium azide and ethyl methane sulphonate (EMS) on the yield of alkaloids, and the anticancer properties of plant extract through in vitro testing. Atropine was isolated via an acid-base extraction process followed by purification and chemical, chromatographic, and non-aqueous titration methods were used to identify and quantify the isolated compound. Using the MTT test, the cytotoxicity of the ethanol extract was evaluated on HEp-2 human epithelial carcinoma cell lines. The findings confirmed successful isolation and purity of atropine. The extract exhibited strong, dose-dependent cytotoxic action, suggesting intriguing anticancer potential, and mutagenesis showed promise in boosting alkaloid synthesis.

References

1. Goodman LS, Gilman A. The pharmacological basis of therapeutics. New York: McGraw-Hill; 1996.

2. Balzarini A, Felisi E, Martini A, De Conno F. Efficacy of homeopathic treatment of skin reactions during radiotherapy for breast cancer: a randomized, double-blind clinical trial. Br Homeopath J. 2000;89(1):8–12.

3. Grabia S, Ernst E. Homeopathic aggravations: a systematic review of randomized, placebo-controlled clinical trials. Homeopathy. 2003;92(2):92–98.

4. Bergmans MG, Merkus JM, Corbey RS, Schellekens LA, Ubachs JM. Effect of Bellergal Retard on climacteric complaints: a double-blind, placebo-controlled study. Maturitas. 1987;9(3):227–234.

5. Bettermann H, Cysarz D, Portsteffen A, Kümmell HC. Bimodal dose-dependent effect on autonomic cardiac control after oral administration of Atropa belladonna. Auton Neurosci. 2001;90(1–2):132–137.

6. Ceha LJ, Presperin C, Young E, et al. Anticholinergic toxicity from nightshade berry poisoning responsive to physostigmine. J Emerg Med. 1997;15(1):65–69.

7. Duncan G, Collison DJ. Role of the non-neuronal cholinergic system in the eye: a review. Life Sci. 2003;72(18–19):2013–2019.

8. Kahn A, Rebuffat E, Sottiaux M, et al. Prevention of airway obstructions during sleep in infants with breath-holding spells by oral belladonna. Sleep. 1991;14(5):432–438.

9. Rastogi RP, Mehrotra BN. Compendium of Indian medicinal plants. Lucknow: CDRI; 1995.

10. Chatterjee A, Chandra PS. The treatise on Indian medicinal plants. New Delhi: CSIR; 1992.

11. Kapoor LD. Handbook of Indian medicinal plants. Boca Raton: CRC Press; 2001.

12. Kirtikar KR, Basu BD. Indian medicinal plants. 2nd ed. Allahabad: Lalit Mohan Basu; 1981.

13. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65(1–2):55–63.

14. Meyer BN, Ferrigni NR, Putnam JE, Jacobsen LB, Nichols DE, McLaughlin JL. Brine shrimp: a convenient general bioassay for active plant constituents. Planta Med. 1982;45(5):31–34.

15. McLaughlin JL. Bench-top bioassays for the discovery of bioactive compounds in higher plants. Brenesia. 1990;34:1–14.

16. Evans WC. Pharmacognosy. 15th ed. Edinburgh: Saunders; 2002.

17. Jain SK, DeFilipps RA. Medicinal plants of India. Michigan: Reference Publications; 1991.

18. Hersey P, Zhang XD. How melanoma cells evade TRAIL-induced apoptosis. Nat Rev Cancer. 2001;1(2):142–150.

19. Taraphdar AK, Roy M, Bhattacharya RK. Natural products as inducers of apoptosis: implication for cancer therapy and prevention. Curr Sci. 2001;80(11):1387–1396.

20. Poncet D, Kroemer G. Chemotherapy targeting the mitochondrial cell death pathway. Oncogene. 2002;21(53):8786–8803.

21. Jayakanthi J, Dhana Rajan MS, Vijaya T, Sarumathya VK. In vitro cytotoxic effect of Atropa acuminata. Int J Pharm Pharm Res. 2015;3(3):1–6.

22. Harborne JB. Phytochemical methods: a guide to modern techniques of plant analysis. 3rd ed. London: Springer; 1998.

23. Wink M. Modes of action of herbal medicines and plant secondary metabolites. Medicines. 2015;2(3):251–286.

24. Pandey KB, Rizvi SI. Plant polyphenols as dietary antioxidants in human health. Oxid Med Cell Longev. 2009;2(5):270–278.

25. Ahmed S, Ikram S. Silver nanoparticles: one-pot green synthesis using plant extracts and its applications. J Adv Res. 2016;7(1):17–28.

26. Trachootham D, Alexandre J, Huang P. Targeting cancer cells by ROS-mediated mechanisms. Nat Rev Drug Discov. 2009;8(7):579–591.

27. Panche AN, Diwan AD, Chandra SR. Flavonoids: an overview. J Nutr Sci. 2016;5:e47.

28. Ramos S. Cancer chemoprevention and chemotherapy: dietary polyphenols and signalling pathways. Mol Nutr Food Res. 2008;52(5):507–526.

29. Scalbert A, Johnson IT, Saltmarsh M. Polyphenols: antioxidants and beyond. Am J Clin Nutr. 2005;81(1 Suppl):215S–217S.

30. Cragg GM, Newman DJ. Natural products: a continuing source of novel drug leads. Biochim Biophys Acta. 2013;1830(6):3670–3695.

31. Newman DJ, Cragg GM. Natural products as sources of new drugs over the last 25 years. J Nat Prod. 2016;79(3):629–661.

32. Greenwell M, Rahman PKSM. Medicinal plants: their use in anticancer treatment. Int J Pharm Sci Res. 2015;6(10):4103–4112.

33. Aggarwal BB, Shishodia S. Molecular targets of dietary agents for prevention and therapy of cancer. Biochem Pharmacol. 2006;71(10):1397–1421.

34. Gottesman MM. Mechanisms of cancer drug resistance. Annu Rev Med. 2002;53:615–627.

35. Heinrich M, Bremner P. Ethnobotany and ethnopharmacy in anti-cancer drug development. Curr Drug Targets. 2006;7(3):239–245.

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Published

30-06-2026

How to Cite

A Comprehensive Review on Cytotoxic Potential of Atropa acuminata. (2026). UNIVERSAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 10(1), 26-31. https://doi.org/10.61114/UJPSR.10.1.2026.26-31