Antiproliferative Effect of Sterols from Resin of Commiphora habessinica
PDF

Keywords

Chloroform fraction, cholesterol, lathosterol, A549 cell lines, GC-MS.

How to Cite

Worku Dinku, Sang Un Choi, Sang-Ho Lee, Young-Sik Jung, ZaeSungNo , & Aman Dekebo. (2019). Antiproliferative Effect of Sterols from Resin of Commiphora habessinica. Journal of Pharmacy and Nutrition Sciences, 9(2), 71–80. https://doi.org/10.29169/1927-5951.2019.09.02.3

Abstract

Commiphora habessinica resin is used traditionally to treat various diseases in Ethiopia. In this study the cytotoxic effects of chloroform fraction and cholesterol and lathosterol isolated from the chloroform fraction of the resin of C. habessinica were evaluated. In the cytotoxicity assay on A549, A2780, MIA-Paca-2, and SNU-638 cell lines, the chloroform fraction showed cytotoxicity ranging from 0.77-3.35 ?g/ml. The chloroform fraction significantly inhibited cell proliferation of A549, A2780, MIA-PaCa-2 and SNU-638, with dose-dependent relation in vitro. The chloroform fraction was more sensitive and has a strongest net growth as percent control effects on A549 cell lines. A mixture of cholesterol : lathosterol (47.9% : 52.1%) exhibited a moderate cytotoxicity which is greater than the individual compound towards A549 and A2780 with IC50 of 13.77 and 20.36 ?g/ml, respectively that might be due to synergetic effect. The GC-MS analysis of chloroform fraction of the resin showed presence of pentacyclic triterpenes as major component (62.98%), sesquiterpene (4.27%), phytosterols (1.53%) and others in trace amount. The isolated compounds from the chloroform fraction were analysed by spectroscopic techniques such as NMR and MS.

https://doi.org/10.29169/1927-5951.2019.09.02.3
PDF

References

Langenheim JH. Plant resins: chemistry, evolution, ecology and ethnobotany. Timber press, Portland, Cambridge, 2003.

Vollesen K. Burseraceae, Flora of Ethiopia, Vol. 3. Addis Ababa University Press, Addis Ababa, 1989; pp. 442-478.

Shen T, Li G-H, Wang X-N, Hong-Xiang Lou H-X. The genus Commiphora: A review of its traditional uses, phytochemistry and pharmacology. J Ethnopharmacol 2012; 142: 319-330. https://doi.org/10.1016/j.jep.2012.05.025

Soromessa T. Ecological Phytogeography: A Case Study of Commiphora Species. Sci Technol Arts Res J 2013; 2(3): 93-104. https://doi.org/10.4314/star.v2i3.98910

Dekebo A, Dagne E, Curry P, et al. Dammarane triterpenes from the resins of Commiphora confusa. Bull Chem Soc Ethiopia 2002a; 16: 81-86. https://doi.org/10.4314/bcse.v16i1.20951

Provan GJ, Waterman PG. The Mansumbinanes: Octanordammaranes from the resins of Commiphora incisa. Phytochemistry 1986; 25: 917-922. https://doi.org/10.1016/0031-9422(86)80027-9

Provan GJ, Waterman PG. Major triterpenes from the resins of Commiphora incisa and C. kua and their potential chemotaxonomic significance. Phytochemistry 1988; 27: 3841-3843. https://doi.org/10.1016/0031-9422(88)83028-0

Dekebo A, Dagne E, Hansen LK, et al. Two octanordammarane triterpenes from Commiphora kua. Phytochemistry 2002b; 59: 399-403. https://doi.org/10.1016/S0031-9422(01)00413-7

Duwiejua M, Zeitlin IJ, Waterman PG, et al. Anti-inflammatory activity of resins from some species of the plant family Burseraceae. Planta Med 1993; 59: 12-16. https://doi.org/10.1055/s-2006-959594

Dekebo A, Lang M, Polborn K, et al. Four lignans from Commiphora erlangeriana. J Nat Prod 2002c; 65: 1252-1257. https://doi.org/10.1021/np020028j

Habtemariam S. Cytotoxic and cytostatic activity of erlangerins from Commiphora erlangeriana. Toxicon 2003; 41: 723-727. https://doi.org/10.1016/S0041-0101(03)00048-5

Gemedo-Dalle T, Maass BL, Isselstein J. Plant biodiversity and ethnobotany of Borana pastoralists in southern Oromia, Ethiopia. Econ Bot 2005; 59(1): 43-65. https://doi.org/10.1663/0013-0001(2005)059[0043:PBAEOB

Tadesse M, Mesin B. A review of selected plants used in the maintenance of health and wellness in Ethiopia. Ee-JRIF 2010; 2: 85-102.

Skehan P, Storeng R, Scudiero D, et al. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst 1990; 82: 1107-1112. https://doi.org/10.1093/jnci/82.13.1107

Wilson WK, Sumpter RM, Warren JJ, et al. Analysis of unsaturated C-27 sterols by nuclear magnetic resonance spectroscopy. J Lipid Res 1996; 37: 1529-1555.

Han Y-H, Ham, J-H, Lee N-J, et al. Antimutagenic activity of 5?-cholest-7-en-3?-ol, a new component from the Starfish Asterina pectinifera. Biol Pharm Bull 2000; 23(10): 1247-1249. https://doi.org/10.1248/bpb.23.1247

Cagnoli BB, Ceccherelli P, Damiani P. Cholesterol, campesterol, and ?-sitosterol from a Commiphora abyssinica. Ann Chim 1968; 58: 541-545.

Patil VD, Nayak UR, Dev S. Chemistry of Ayurvedic crude drugs-I: Guggulu (resin from Commiphora mukul)-1: steroidal constituents. Tetrahedron 1972; 28: 2341-2352. https://doi.org/10.1016/S0040-4020(01)93577-X

Agarwal RC, Singh SP, Saran RK, et al. Clinical trial of gugulipid—a new hypolipidemic agent of plant origin in primary hyperlipidemia. Indian J Med Res 1986; 84: 626.

Khanna D, Sethi G, Ahn KS, et al. Natural products as a gold mine for arthritis treatment. Curr Opin Pharmacol 2007; 7: 344. https://doi.org/10.1016/j.coph.2007.03.002

Singh RB, Niaz MA, Ghosh S. Hypolipidemic and antioxidant effects of Commiphora mukul as an adjunct to dietary therapy in patients with hypercholesterolemia. Cardiovasc Drugs Ther 1994; 8: 659. https://doi.org/10.1007/BF00877420

Urizar NL, Moore DD. GUGULIPID: a natural cholesterol-lowering agent. Annu Rev Nutr 2003; 23: 303. https://doi.org/10.1146/annurev.nutr.23.011702.073102

Mencarelli A, Barbara RB, Palladino G, et al. The plant sterol guggulsterone attenuates inflammation and immune dysfunction in murine models of inflammatory bowel disease. Biochem Pharmacol 2009; 78: 1214-1223. https://doi.org/10.1016/j.bcp.2009.06.026

Bhat AB, Prabhu KS, Kuttikrishnan S, et al. Potential therapeutic targets of guggulsterone in cancer. Nutr Metab 2017; 14(23): 1-11. https://doi.org/10.1186/s12986-017-0180-8

Erasto P. Antimycobacterial sterols from aromatic stem sap of Commiphora eminii Engl. J Adv Sci Res 2012; 3(4): 27-31.

Smith AG, Rubinstein I, Goad LJ. The sterols of the echinoderm Asterias rubens. Biochem J 1973; 135: 443-455. https://doi.org/10.1042/bj1350443

Smith AG, Goad LJ. The conversion of cholest-5-en-3?-ol into cholest-7-en-3?-ol by the echinoderms Asterias rubens and Solaster papposus. Biochem J 1975; 146: 35-40. https://doi.org/10.1042/bj1460035

Smith AG, Goad LJ. Sterol biosynthesis in the Starfish Asterias rubens and Henricia sanguinolenta. Biochem J 1971; 123: 671-673. https://doi.org/10.1042/bj1230671

Goad LJ, Rubinstein I, Smith AG. Sterols and bile acids. Proc Roy Soc Ser B 1972; 180: 223-246.

Fagerlund UHM, Idler DR. Marine sterols. Sterol biosynthesis in molluscs and echinoderms.Can J Biochem Physiol 1960; 38: 997-1002. https://doi.org/10.1139/y60-124

Kamal-Eldin K, Moazzami A. Plant sterols and stanols as cholesterol-lowering ingredients in functional foods. Recent Pat Food Nutr Agric 2009; 1: 1-14. https://doi.org/10.2174/2212798410901010001

Vázquez LH, Palazon J, Navarro-Ocaña A. The pentacyclic triterpenes ?,?-amyrins: A review of sources and biological activities. In phytochemicals-A global perspective of their role in nutrition and health 2012; InTech.

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Copyright (c) 2019 Worku Dinku , Sang Un Choi , Sang-Ho Lee , Young-Sik Jung , Zae Sung No  , Aman Dekebo