Protective effects of Nigella sativa against 7,12-dimethylbenz [á] anthracene (DMBA) induced carcinogenesis in rats

Main Article Content

Nur Fatmi Alisah
Hanif Nasiatul Baroroh
Heny Ekowati

Abstract

Background
Liver cancer is the third most common cause of death from cancer worldwide. Recently, natural products have been widely used as an alternative therapy for liver cancer. Previous studies have reported that Nigella sativa has chemopreventive activity in vitro and in vivo. The objective of this study was to evaluate the effect of a chloroform extract of Nigella sativa seeds (NSS) on female rat hepatocytes after administration of 7,12-dimethylbenz [á] anthracene (DMBA).

Methods
The experimental design comprised five groups of rats. Group I (DBMA control group) received oral DMBA at a dosage of 20 mg/kgBW twice weekly for five weeks, while group V (solvent control group) was given corn oil only. The other three groups received DMBA + NSS at dosages of 250 mg/kgBW, 500 mg/kgBW, and 750 mg/kgBW, respectively. Each group consisted 12 rats. The NSS extract dissolved in corn oil was administered daily by the oral route for 2 weeks before and subsequenyly during DMBA tumor induction. At the end of the study, rat livers were collected and stained with hematoxylin and eosin (H&E) and silver staining by the the AgNOR method.

Results
There was a difference in liver tissue histopathological profile between the NSS, DMBA control, and the solvent control group. AgNOR counts in the DMBA control group, the DMBA+NSS 250 mg/kgBW group, DMBA+NSS 500 mg/kgBW group, and DMBA+NSS 750 mg/kgBW group were 1.79, 1.51, 1.41, and 1.35, respectively.

Conclusion
Nigella sativa seed extract was able to reduce the liver damage and proliferation in rats induced by DMBA administration.

Article Details

How to Cite
Alisah, N. F., Baroroh, H. N., & Ekowati, H. (2012). Protective effects of Nigella sativa against 7,12-dimethylbenz [á] anthracene (DMBA) induced carcinogenesis in rats. Universa Medicina, 31(2), 88–95. https://doi.org/10.18051/UnivMed.2012.v31.88-95
Section
Review Article

References

Hope S. Rugo MD. Cancer. In: Current medical diagnosis and treatment. New York: McGraw-Hill;2008.p.1387-458.

Ruddon RW. The epidemiology of human cancer. In: Cancer biology, 4nd ed. New York: Oxford University Press Inc;2007.p.70-116.

Greenwald P. Cancer chemoprevention. BMJ 2002;324:714–8.

Nickavar B, Mojab F, Javidnia K, Amoli MAR. Chemical composition of the fixed and volatile oils of Nigella sativa L. from Iran. Z Naturforsch 2003;58c:629-31.

Ekowati H, Prasasti E, Rastuti U. The Active fraction from Nigella sativa and its activity against T47D cell line. Indo J Chem 2011;20: 217-22.

Nazrul SK, Begum F, Ahsan T, Saiful HMA. Immunosuppressive and cytotoxic properties of Nigella sativa. Phytother Res 2004;18:395-8.

Al-Naggar TB, Serranillos GMP, Carreto ME, Villar AM. Neuropharmacological activity of Nigella sativa L. extract. J Ethnopharmacol 2003;88:63-8.

Mohtashami R, Amini M, Huseini F, Ghamarchehre M, Sadeqhi Z, Hajiagaee R, et al. Blood glucose lowering effects of Nigella sativa L. seeds oil in healthy volunteers: a randomized, double-blind, placebo-controlled clinical trial. J Med Plants 2011;10:1-5.

Rooney S, Ryan MF. Effects of alpha-hederin and thymoquinone – a constituent of Nigella sativa, on human cancer cell lines. Anticancer Res 2005;25:2197-204.

Salim EI, Fukushima S. Chemopreventive potential of volatile oil from black cumin (Nigella sativa) seeds against rat colon carcinogenesis. Nutr Cancer 2003;45:195-202.

Mohamed HA, El-Sayed IH, Moawad M. Protective effect of Nigella sativa seeds against dimethylaminoazobenzene (DAB) induced liver carcinogenesis. Nat Sci 2010;8:80-7.

Mbarek LA, Mouse HA, Elabbadi N, Bensalah M, Gamouh A, Aboufatima, R, et al. Anti-tumor properties of blackseed (Nigella sativa L.) extracts. Braz J Med Biol Res 2007;40:839-47.

Daoud M, Nihat D, Hatice G, Gulruh U, Muharrem B. Antitumor activity of an ethanol extract of N. sativa seeds. Biol Brat 2004;59:735-40.

Shoieb AM, Elgayyari M, Dudrick PS, Bell JL, Tithof PK. In vitro inhibition of growth and induction of apoptosis in cancer cell lines by thymoquinone. Int J Oncol 2003;22:107-13.

Silva BAK, Silva IS, Pereira DM, Aydos RD, Carvalho PTC. Usefulness of argyrophilic nucleolar organizer regions in detection of lung cells alterations after benzo[a]pyrene instillation. Acta Cir Bras 2006;21 Suppl 4:S36-9.

Muqbil I, Banu N. Enchancement of pro-oxodant effect of 7,12-dimethylbenz (a) anthracene (DMBA) in rats by pre-exposure to restraint stress. Cancer Lett 2006;240:213-20.

Shimada T, Kuriyama FY. Metabolic activation of polycyclic aromatic hydrocarbons to carcinogens by cytochromes P450 1A1 and 1B1. Cancer Sci 2004;95:1-6.

Shimada T, Guengerich FP. Inhibition of human cytochrome P450 1A1-, 1A2-, and 1B1-mediated activation of procarcinogens to genotoxic metabolites by polycyclic aromatic hydrocarbons. Chem Res Toxicol 2006;19:228-94.

Patri M, Padmini P. Polycyclic aromatic hydrocarbons in air and their neurotoxic potency in assosiation with oxidative stress: a brief perspective. Ann Neurosci 2009;16:340-9.

Al-Attar MA. The influence of dietary grapeseed oil on DMBA-induced liver enzymes disturbance in the frog, Rana ridibunda. Pakistan J Nutr 2004;3:304-9.

Golstein P, Kroemer G. Cell death by necrosis: towards a molecular definition. Sci Dir 2006;32: 37-43.

Naugler WE, Sakurai T, Kim S, Maeda S, Kim K, Elsharkawy AM, et al. Gender disparity in liver cancer due to sex differences in MyD88-dependent IL-6 production. Sci 2007;317:121–4.

Simopoulos AP. The omega-6/omega-3 fatty acid ratio, genetic variation, and cardiovascular disease. Asia Pac J Clin Nutr 2008;17:131-4.

Maggiora M, Bologna M, Ceru MP, Possati L, Angelucci A, Cimini A, et al. An overview of the effect of linoleic and conjugated linoleic acids on the growth of several human tumor cell lines. J Int Cancer 2004;112:909-19.

Zhang Y, Xue R, Zhang Z, Yang X, Shi H. Palmitic and linoleic acids induce ER stress and apoptosis in hepatoma cells. Lipids Health Dis 2012;11:1-8.