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诺考达唑对雄性小鼠生殖细胞的显性致死效应。

Dominant lethal effects of nocodazole in germ cells of male mice.

作者信息

Attia S M, Ahmad S F, Okash R M, Bakheet S A

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. 2457, Riyadh 11451, Saudi Arabia; Department of Pharmacology and Toxicology, College of Pharmacy, Al-Azhar University, Cairo, Egypt.

Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. 2457, Riyadh 11451, Saudi Arabia.

出版信息

Food Chem Toxicol. 2015 Mar;77:101-4. doi: 10.1016/j.fct.2015.01.004. Epub 2015 Jan 13.

Abstract

The ability of the anticancer drug, nocodazole, to induce dominant lethal mutations in male germ cells was investigated by the in vivo dominant lethal test. Mice were treated with single doses of 15, 30 and 60 mg/kg nocodazole. These males were mated at weekly intervals to virgin females for 6 weeks. Nocodazole clearly induced dominant lethal mutations in the early spermatid stage with the highest tested dose. Mice treated with 60 mg/kg nocodazole showed an additional peak of dominant lethal induction in mature spermatozoa during the first week matings after treatment. The percentage sperm count and sperm motility were significantly decreased after treatment of males with 30 and 60 mg/kg nocodazole. Moreover, the middle and highest doses of nocodazole significantly increased the percentage of abnormal sperm. Our study provides evidence that nocodazole is a germ cell mutagen. Marked alteration in the spermiogram analysis after nocodazole treatment possibly confirms that nocodazole has a significant effect on sperm maturation and development during storage and transit. The demonstrated mutagenicity profile of nocodazole may support further development of effective chemotherapy with less mutagenicity. Moreover, the cancer patients and medical personnel exposed to this drug chemotherapy may stand a higher risk for abnormal reproductive outcomes.

摘要

通过体内显性致死试验研究了抗癌药物诺考达唑诱导雄性生殖细胞显性致死突变的能力。给小鼠单次注射15、30和60mg/kg的诺考达唑。这些雄性小鼠每周与未交配过的雌性小鼠交配,持续6周。诺考达唑在最高测试剂量下明显诱导早期精子细胞阶段的显性致死突变。用60mg/kg诺考达唑处理的小鼠在处理后的第一周交配期间,成熟精子中出现了另一个显性致死诱导高峰。用30和60mg/kg诺考达唑处理雄性小鼠后,精子计数百分比和精子活力显著降低。此外,诺考达唑的中高剂量显著增加了异常精子的百分比。我们的研究提供了证据表明诺考达唑是一种生殖细胞诱变剂。诺考达唑处理后精子图分析的明显改变可能证实诺考达唑在储存和运输过程中对精子成熟和发育有显著影响。所证明的诺考达唑的诱变性特征可能支持进一步开发具有较低诱变性的有效化疗方法。此外,接触这种药物化疗的癌症患者和医务人员可能面临更高的生殖异常风险。

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