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评价抗肥胖药物西布曲明和芬氟拉明的遗传毒性和细胞毒性作用。

An evaluation of the genotoxic and cytotoxic effects of the anti-obesity drugs sibutramine and fenproporex.

机构信息

Department of Genetics, Faculty of Medicine of Ribeirão Preto, São Paulo University, São Paulo, Brazil.

出版信息

Hum Exp Toxicol. 2010 Mar;29(3):187-97. doi: 10.1177/0960327109358732. Epub 2010 Jan 5.

Abstract

Anti-obesity medications deserve special considerations at the present time due to an increasing number of overweight and obese people who require these therapeutic alternatives. Obesity is positively associated with several chronic illnesses, including cancer. In this work, we evaluated the possible genotoxic and/or cytotoxic actions of two drugs, sibutramine and fenproporex, in the doses of 10, 20 and 40 mg/kg body weight (bw), administered intraperitoneally in male Swiss mice. The genotoxic effect was analyzed by comet assay and micronucleus test. We found that both drugs increased the frequency of genotoxic damage in Swiss mice, but did not present cytotoxic activities towards the polychromatic erythrocytes of the bone marrow of these animals.

摘要

由于越来越多的超重和肥胖人群需要这些治疗选择,抗肥胖药物目前应得到特别考虑。肥胖与多种慢性疾病呈正相关,包括癌症。在这项工作中,我们评估了两种药物(西布曲明和芬氟拉明)在 10、20 和 40 mg/kg 体重(bw)的剂量下的潜在遗传毒性和/或细胞毒性作用,这些药物通过腹腔注射给予雄性瑞士小鼠。通过彗星试验和微核试验分析遗传毒性作用。我们发现这两种药物都增加了瑞士小鼠的遗传毒性损伤频率,但对这些动物骨髓的多色红细胞没有细胞毒性作用。

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