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阿托品诱导毒性大鼠睾丸中ACE和ABCG2表达水平的变化。

Alterations in ACE and ABCG2 expression levels in the testes of rats subjected to atropine-induced toxicity.

作者信息

Li Xue-Fang, Huang Quan-Yong, Yang Wen-Zhong, Wang Hui-Jie, Li Can-Wei

机构信息

Library of Dali University, Dali, Yunnan 671003, P.R. China.

Department of Pathology, School of Basic Medical Sciences, Dali University, Dali, Yunnan 671000, P.R. China.

出版信息

Mol Med Rep. 2016 Dec;14(6):5211-5216. doi: 10.3892/mmr.2016.5857. Epub 2016 Oct 19.

Abstract

Atropine-induced damage is associated with enzyme and protein alterations. The aim of the present study was to investigate atropine‑induced alterations in testicular expression levels of angiotensin‑converting enzyme (ACE) and adenosine 5'-triphosphate binding cassette sub‑family G member 2 (ABCG2) following atropine treatment. Male Wistar rats received 15 mg/kg/day atropine for 7 days; control rats received an identical volume of saline, Following treatment, the testes were harvested for immunohistochemistry and in situ hybridization to examine the protein and gene expression levels of ACE and ABCG2 by digital image analysis. ACE gene and protein expression levels were significantly reduced in the testes of atropine‑treated rats, compared with control rats (P=0.0001 and P<0.001, respectively). In addition, ABCG2 gene and protein expression levels were significantly increased in the testes of atropine‑treated rats, compared with control rats (P=0.0017 and P<0.001, respectively). Thus, the results of the present study demonstrate that testicular protein and gene expression levels of ACE and ABCG2 were altered as a result of atropine‑induced toxicity in the rats. These alterations may result in abnormal testicular function, and the proteins and genes identified in the present study may be useful to elucidate the mechanisms underlying atropine‑induced toxicity and provide a direction for further studies.

摘要

阿托品诱导的损伤与酶和蛋白质的改变有关。本研究的目的是调查阿托品治疗后睾丸中血管紧张素转换酶(ACE)和三磷酸腺苷结合盒亚家族G成员2(ABCG2)表达水平的变化。雄性Wistar大鼠接受15mg/kg/天的阿托品治疗7天;对照大鼠接受相同体积的生理盐水。治疗后,收集睾丸进行免疫组织化学和原位杂交,通过数字图像分析检测ACE和ABCG2的蛋白质和基因表达水平。与对照大鼠相比,阿托品处理大鼠睾丸中ACE基因和蛋白质表达水平显著降低(分别为P = 0.0001和P < 0.001)。此外,与对照大鼠相比,阿托品处理大鼠睾丸中ABCG2基因和蛋白质表达水平显著升高(分别为P = 0.0017和P < 0.001)。因此,本研究结果表明,大鼠睾丸中ACE和ABCG2的蛋白质和基因表达水平因阿托品诱导的毒性而发生改变。这些改变可能导致睾丸功能异常,本研究中鉴定的蛋白质和基因可能有助于阐明阿托品诱导毒性的潜在机制,并为进一步研究提供方向。

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