Investigation of the Effects of Harmine Alkaloid on Bovine Oocyte in Vitro Maturation
Subject Areas : Journal of Animal BiologyZ. Hemmati 1 , M. Heydari Nasrabadi 2 , P. Khodarahmi 3
1 - Department of Biology, Parand Branch, Islamic Azad University, Parand, Iran
2 - Department of Biology, Parand Branch, Islamic Azad University, Parand, Iran
3 - Department of Biology, Parand Branch, Islamic Azad University, Parand, Iran
Keywords: In vitro maturation, Alkaloids harmine, Bovine oocyte,
Abstract :
In vitro maturation of oocytes is the technique that can reduce costs and eliminate the side effects of the use of gonadotropins for in vitro fertilization. Conducting research on the development and improvement of in vitro culture conditions for human oocyte maturation is very difficuly. The use domestic animals has provided the most advanced and best system to study the maturation of immature follicles in the laboratory. Due to the active ingredient in the harmine alkaloid with multiple pharmacological effects including anti-free radical, anti-inflammation and immune system, etc., the present study assesses the effects of harmine alkaloid on bovine oocyte maturation. In this study, at least three layers of cumulus oocytes aspirated from 2-8 mm follicles obtained from bovine ovaries from slaughterhouses after three washes in the washing environment were incubated for 22-24 hours in maturation environments with different concentrations of 0.5, 1, 2.5, and 5 µg/ml of the alkaloid harmine at a temperature of 38.5 ° C with 5% carbon dioxide. After a while, the cumulus incubation was removed from surrounding eggs were removed and the release of polar corpuscle (maturity) was assessed. Results were evaluated using SPSS and ANOVA. Research results showed the positive impact of the alkaloid harmine at 1 µg/ml (p <0.05) such that the maturity of the groups treated with doses of 0.5, 1, 2.5 and 5 micrograms per milliliter were 59.85, 72.65, 64.34, and 37.22 percent, respectively, which was 56.93 percent in the control group. Adding 1 µg/ml of alkaloids harmine led to the maturity environment increased the maturation of the bovine oocytes, which can be used as a supplement in oocyte maturation environments.
1. Aitken R.J., Harkiss D., Buckingham D., 1993. Relationship between irons catalysed lipid peroxidation potential a human sperm function. Journal of reproduction and fertility, 98: 257-65.
2. Bouayad N., Rharrabe K., Lamhamdi M., Nourouti N.G., Sayah F., 2011. Dietary effects of harmine, a β-carboline alkaloid, on development, energy reserves and a amylase activity of Plodia interpunctella Hübner [Lepidoptera: Pyralidae]. Saudi Journal ofBiological Sciences, 19(1): 73-80.
3. Callaway J.C, McKenna D.J., Grob C.S., Brito G.S., Raymon L.P., Poland R.E., Andrade E.N., Andrade E.O., Mash D.C., 1999. Pharmacokinetics of hoasca alkaloids in healthy humans. Journal of Ethnopharmacology, 65: 243–256.
4.Chian R.C., Niwa K., Sirard M.A., 1994. Effects of cumulus cells on male pronuclear formation and subsequent early development of bovine oocytes In vitro. Theriogenology. 41: 1499–1508.
5. Comporti M., 1986. Three models of free radical induced cell injury. Chemico-Biological Interactions, 72: 472-7.
6. Fuentes J.A., Longo V.G., 1971. An investigation on the central effects of harmine, harmaline and related beta-carbolines. Neuropharmacology, 10(1):15-23.
7. Gordon I., 2005. Reproductive technology in farm animals, CABI publication.
8. Hreinsson J.R., Friden B., Levkov L., Recombinant L.H., 2003. Is equally effective as recombinant hCG in promoting oocyte maturation in clinical In vitro maturation programme: a randomized study. Hum Repro, 18: 2131-2136.
9. Ishida J., Wang H.K., Bastow K.F., Huc Q., Lee K.H., 1999. Anti-tumor agents (201) cytotoxicity of Harmine and B-Carboline analogs. Bioorganic & Medicinal Chemistry Letters, 9(23): 3319-3324.
10. Kartal M., Alton M.L., Kurusu S, 2003 HPLC metod for the analysis of harmol, harmalol, harmine and harmalin in the seeds of peganum harmala L Parmaceut Biomedical Analysis, 2: 263-269
11. Meister A., 1983. Selective modification of glutathione metabolism. Sience, 220: 472-7.
12. Nadi S., Ravindranatha B.M., Gupta P.S.P., Sarma P.V. 2002. Timing of sequential changes in cumulus cells and first polar body extrusion during In vitro maturation of buffalo oocytes. Theriogenology, 57: 1151 – 1159.
13. Pérez Martín J.M., Labrador V., Fernández Freire P., Molero M.L., Hazen M.J., 2004. Ultrastructural changes induced in HeLa cells after phototoxic treatment with harmine. Journal of Applied Toxicology, 24(3): 197–201.
14. Roa B.S., Naidu K.S., Amarnath D., Vagdevi R., 2002. In vitro maturation of sheep oocytes in different media during breeding and non-breeding seasons. Small Rumin Research, 43: 31-36.
15. Saeki K., Hoshi M., Leibfried L., First N.L., 1991. In vitro fertilization and development of bovine oocytes matured in seum-free medium. Biology Reproduction, 44: 256-260.
16. Sun Q., Nagai T., 2003. Molecular mechanisms underlying pig oocyte maturation and fertilization. Journal of Reproduction and Development, 49: 347-359.
17. Zhao L., Wink M., 2013. The carboline alkaloid harmine inhibits telomerase activity of MCF-7 cells by down-regulating hTERT mRNA expression accompanied by an accelerated senescent phenotype, Journal of Life and Environmental Sciences 1:e174; DOI 10.7717/peerj.174
_||_