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[甲醛对雌性大鼠卵巢组织Fas凋亡通路相关基因表达的影响]

[Effect of formaldehyde on expressions of Fas apoptosis pathway-related genes of ovary tissues in female rats].

作者信息

Peng Guoqing, Zhong Caigao, Zhang Qiong, Xie Ying, Gong Fengying

机构信息

Department of Toxicology, School of Public Health, Central South University, Changsha 410078, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2010 Apr;35(4):341-5. doi: 10.3969/j.issn.1672-7347.2010.04.010.

Abstract

OBJECTIVE

To explore the mechanism of formaldehyde inducing ovarian toxicity in female rats by observing the effect of formaldehyde on the expression of Fas and caspase-8 mRNA, and the activity of caspase-3 and caspase-8 of ovary tissues in female rats.

METHODS

Forty female Sprague-Dawley(SD) rats were randomly divided into a control group and 3 formaldehyde groups at different concentrations. The rats in the formaldehyde groups were intraperitoneally injected different doses of formaldehyde (20.0,2.0 and 0.2 mg/kg) continuously for 14 days.After 14 days, all rats were sacrificed and their ovaries were collected for detecting the expression of Fas and caspase-8 mRNA with RT-PCR, the protein expression of Fas with Western blot, and the activities of caspase-8 and caspase-3 with spectrophotometric method.

RESULTS

Compared with the control group, the expression of Fas mRNA and its protein and caspase-8 mRNA and the activity of caspase-8 and caspase-3 of ovary tissues in the rats treated with formaldehyde significantly increased with dose (P<0.05).

CONCLUSION

The increase of Fas gene expression and the activity of caspase-8 and caspase-3 may be the important mechanism of ovarian toxicity induced by formaldehyde in female rats.

摘要

目的

通过观察甲醛对雌性大鼠卵巢组织中Fas和caspase-8 mRNA表达以及caspase-3和caspase-8活性的影响,探讨甲醛诱导雌性大鼠卵巢毒性的机制。

方法

将40只雌性Sprague-Dawley(SD)大鼠随机分为对照组和3个不同浓度的甲醛组。甲醛组大鼠连续14天腹腔注射不同剂量的甲醛(20.0、2.0和0.2 mg/kg)。14天后,处死所有大鼠,采集卵巢,用RT-PCR检测Fas和caspase-8 mRNA的表达,用Western blot检测Fas蛋白表达,用分光光度法检测caspase-8和caspase-3的活性。

结果

与对照组相比,甲醛处理大鼠卵巢组织中Fas mRNA及其蛋白、caspase-8 mRNA的表达以及caspase-8和caspase-3的活性随剂量显著增加(P<0.05)。

结论

Fas基因表达以及caspase-8和caspase-3活性的增加可能是甲醛诱导雌性大鼠卵巢毒性的重要机制。

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