{"title":"芹菜素对醋酸环丙孕酮致人淋巴细胞染色体损伤的抗基因毒性作用","authors":"Y. Siddique, M. Afzal","doi":"10.5580/242e","DOIUrl":null,"url":null,"abstract":"Cyproterone acetate (CPA) is not only a genotoxic agent but also a tumor initiating agent. It is used in oral contraceptives formulations and also in the treatment various sexual and metabolic disorders. Apigenin, a well known antioxidant and have number of properties that are beneficial in someway to humans. In this context, the antigenotoxic effect of apigenin was studied against the genotoxic doses of CPA using chromosomal aberrations, sister chromatid exchanges and cell cycle kinetics as parameters. The treatment of 20 and 30 M of CPA was given separately along with apigenin at the doses of 1, 5, 10 and 20 M of culture medium. A clear dose dependent decrease in the genotoxic damage of CPA was observed, suggesting a protective role of apigenin during CPA therapy. The results of the present study suggest that the apigenin can modulate the genotoxicity of CPA on human lymphocytes in vitro.","PeriodicalId":22523,"journal":{"name":"The Internet Journal of Pharmacology","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2007-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antigenotoxic effect of apigenin on chromosomal damage induced by cyproterone acetate in human lymphocytes\",\"authors\":\"Y. Siddique, M. Afzal\",\"doi\":\"10.5580/242e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cyproterone acetate (CPA) is not only a genotoxic agent but also a tumor initiating agent. It is used in oral contraceptives formulations and also in the treatment various sexual and metabolic disorders. Apigenin, a well known antioxidant and have number of properties that are beneficial in someway to humans. In this context, the antigenotoxic effect of apigenin was studied against the genotoxic doses of CPA using chromosomal aberrations, sister chromatid exchanges and cell cycle kinetics as parameters. The treatment of 20 and 30 M of CPA was given separately along with apigenin at the doses of 1, 5, 10 and 20 M of culture medium. A clear dose dependent decrease in the genotoxic damage of CPA was observed, suggesting a protective role of apigenin during CPA therapy. The results of the present study suggest that the apigenin can modulate the genotoxicity of CPA on human lymphocytes in vitro.\",\"PeriodicalId\":22523,\"journal\":{\"name\":\"The Internet Journal of Pharmacology\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Internet Journal of Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5580/242e\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Internet Journal of Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5580/242e","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Antigenotoxic effect of apigenin on chromosomal damage induced by cyproterone acetate in human lymphocytes
Cyproterone acetate (CPA) is not only a genotoxic agent but also a tumor initiating agent. It is used in oral contraceptives formulations and also in the treatment various sexual and metabolic disorders. Apigenin, a well known antioxidant and have number of properties that are beneficial in someway to humans. In this context, the antigenotoxic effect of apigenin was studied against the genotoxic doses of CPA using chromosomal aberrations, sister chromatid exchanges and cell cycle kinetics as parameters. The treatment of 20 and 30 M of CPA was given separately along with apigenin at the doses of 1, 5, 10 and 20 M of culture medium. A clear dose dependent decrease in the genotoxic damage of CPA was observed, suggesting a protective role of apigenin during CPA therapy. The results of the present study suggest that the apigenin can modulate the genotoxicity of CPA on human lymphocytes in vitro.