4.6 Article

Cytotoxic activity of the chemical constituents of Clerodendrum indicum and Clerodendrum villosum roots

Journal

JOURNAL OF INTEGRATIVE MEDICINE-JIM
Volume 16, Issue 1, Pages 57-61

Publisher

ELSEVIER
DOI: 10.1016/j.joim.2017.12.004

Keywords

Clerodendrum indicum; Clerodendrum villosum; Cytotoxicity; Triterpenoids; Steroids; Flavonoids; Plants, medicinal

Funding

  1. Research Institute of Rangsit University [40/2556]

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Objective: The roots of two Thai medicinal plants, Clerodendrum indicum and Clerodendrum villosum are found in traditional medicine practices. The aim of this research was to preliminarily study the cytotoxicity of extracts of their roots, and the parts that possessed cytotoxic activity were separated on a chromatograph to identify their active compounds. Methods: The extracts of both plants were screened for cytotoxicity on the SW620 cell line and the compounds isolated from the active extracts were further evaluated for their cytotoxic activity against five human cancer cell lines, including SW620, ChaGo-K-1, HepG2, KATO-III and BT-474 using the 3-(4,5-dime thyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay. Results: Dichloromethane extracts of C. indicum and C. villosum were active against the SW620 cell line. Triterpenoids were mostly obtained from the extracts of these plants (0.28% and 1.02%, respectively) and exhibited varying degrees of cytotoxicity and specificity against the tested cell lines. Two triterpenoids, oleanolic acid 3-acetate and betulinic acid, displayed moderate to strong cytotoxicity toward all cancer cell lines, with 50% inhibitory concentration (IC50) values of 1.66-20.49 mmol/L, whereas 3 beta-hydroxyD:B-friedo-olean-5-ene and taraxerol were cytotoxic to only the SW620 cell line (IC50 = 23.39 and 2.09 mmol/L, respectively). Triterpenoid, lupeol, showed potent cytotoxicity on both SW620 (IC50 = 1.99 mmo l/L) and KATO-III cell lines (IC50 = 1.95 mmol/L),while a flavonoid, pectolinarigenin, displayed moderate cytotoxicity against these cells (IC50 = 13.05 and 24.31 mmol/L, respectively). Although the widely distributed steroid, stigmasterol, was effective against the SW620 cell line (IC50 = 2.79 mmol/L) and bsitosterol was also active against SW620 (IC50 = 11.26 mmol/L), BT-474 (IC50 = 14.11 mmol/L) and HepG2 cancer cells (IC50 = 20.47 mmol/L), none of the characteristic 24b-ethylsteroids of either Clerodendrum species were shown to be cytotoxic. Conclusion: This study is the first report on the presence of cytotoxic triterpenoids from the roots of these medicinal plants, which have been used in herbal formulas as an antipyretic. Our findings support further in-depth study of this pharmacological activity as an anticancer agent. (C) 2017 Shanghai Changhai Hospital. Published by Elsevier B.V. All rights reserved.

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