N. S. Reddy, P. Nirmala, N. Chidambaram, Patidar Ashok Kumar
{"title":"Quercetin in Dimethyl Benzanthracene Induced Breast Cancer in Rats","authors":"N. S. Reddy, P. Nirmala, N. Chidambaram, Patidar Ashok Kumar","doi":"10.3844/AJPTSP.2012.68.72","DOIUrl":null,"url":null,"abstract":"Problem statement: Vincristine a commonly used anticancer agent in th e treatment of breast cancer results in serious adverse effects li ke teratogenicity, neurotoxicity and carcinogenicit y on long term use. Drug resistance is also a common pro blem encountered with vincristine. Hence the effect of flavonol quercetin, a known antioxidant w ith no known documented adverse effect was tried in treatment of DMBA induced breast cancer in female rats and its effect was compared with vincristine. Approach: Quercetin at the dose of 50, 100-200 mg kg -1 body weight was administered in DMBA induced breast cancer in female wistar rats and its effects were compared with Vincristine. The anti oxidant enzymes, catalase, glutathione peroxid ase and superoxide dismutase and Thiobarbituric Acid Reactive Substances (TBARS) level in cancerous breast tissue, TBARS and catalase in plasma and superoxide dismutase and glutathione peroxidase in erythrocyte lysate were estimated. Results: Quercetin supplementation at the dose of 100 mg kg -1 body weight was most effective in alleviating cancer symptoms and was comparable to vincristine. The plasma TBARS were reduced and breast tissue TBARS were elevated. The antioxidant enzymes were rejuvenated by quercetin supplementation at all three dose levels. Conclusion: Quercetin is found to be an effective chemotherape utic agent in the treatment of breast cancer on par with vincrist ine. Being a plant product, quercetin can also be u sed in chemoprophylaxis in high risk individuals with g enetic predisposition towards breast cancer. Besides, it can be given orally and has a wide marg in of safety.","PeriodicalId":7769,"journal":{"name":"American Journal of Pharmacology and Toxicology","volume":"15 1","pages":"68-72"},"PeriodicalIF":0.0000,"publicationDate":"2012-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Pharmacology and Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3844/AJPTSP.2012.68.72","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13
Abstract
Problem statement: Vincristine a commonly used anticancer agent in th e treatment of breast cancer results in serious adverse effects li ke teratogenicity, neurotoxicity and carcinogenicit y on long term use. Drug resistance is also a common pro blem encountered with vincristine. Hence the effect of flavonol quercetin, a known antioxidant w ith no known documented adverse effect was tried in treatment of DMBA induced breast cancer in female rats and its effect was compared with vincristine. Approach: Quercetin at the dose of 50, 100-200 mg kg -1 body weight was administered in DMBA induced breast cancer in female wistar rats and its effects were compared with Vincristine. The anti oxidant enzymes, catalase, glutathione peroxid ase and superoxide dismutase and Thiobarbituric Acid Reactive Substances (TBARS) level in cancerous breast tissue, TBARS and catalase in plasma and superoxide dismutase and glutathione peroxidase in erythrocyte lysate were estimated. Results: Quercetin supplementation at the dose of 100 mg kg -1 body weight was most effective in alleviating cancer symptoms and was comparable to vincristine. The plasma TBARS were reduced and breast tissue TBARS were elevated. The antioxidant enzymes were rejuvenated by quercetin supplementation at all three dose levels. Conclusion: Quercetin is found to be an effective chemotherape utic agent in the treatment of breast cancer on par with vincrist ine. Being a plant product, quercetin can also be u sed in chemoprophylaxis in high risk individuals with g enetic predisposition towards breast cancer. Besides, it can be given orally and has a wide marg in of safety.
问题陈述:长春新碱是治疗乳腺癌常用的抗癌药物,长期使用会产生致畸、神经毒性、致癌性等严重不良反应。耐药性也是长春新碱遇到的一个常见问题。因此,黄酮醇槲皮素,一种已知的抗氧化剂,没有已知的不良反应,被用于治疗雌性大鼠DMBA诱导的乳腺癌,并与长春新碱进行了比较。方法:采用槲皮素50、100 ~ 200 mg kg -1体重剂量对DMBA诱导的雌性wistar大鼠乳腺癌进行治疗,并与长春新碱进行比较。测定癌性乳腺组织中抗氧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、超氧化物歧化酶和硫代巴比妥酸活性物质(TBARS)水平,血浆中TBARS和过氧化氢酶水平,红细胞裂解液中超氧化物歧化酶和谷胱甘肽过氧化物酶水平。结果:槲皮素补充剂量为100 mg kg -1体重对缓解癌症症状最有效,与长春新碱相当。血浆TBARS降低,乳腺组织TBARS升高。槲皮素在三种剂量水平下均能使抗氧化酶恢复活力。结论:槲皮素是一种与长春素相当的治疗乳腺癌的有效化疗药物。作为一种植物产品,槲皮素也可用于具有乳腺癌遗传易感性的高危人群的化学预防。此外,它可以口服,有很大的安全范围。