氯丙嗪诱导毒性作用后大鼠心脏中 E-钙黏蛋白和窖蛋白-1 的改变。

E-cadherin and caveolin-1 alterations in the heart of rats having undergone chlorpromazine-induced toxicity.

机构信息

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

出版信息

Mol Med Rep. 2012 Mar;5(3):705-9. doi: 10.3892/mmr.2011.729. Epub 2011 Dec 20.

Abstract

Heart damage induced by chlorpromazine (CPZ) toxicity is associated with changes in the expression of various enzymes and proteins. This study aimed to investigate CPZ‑induced alterations in cardiac E-cadherin and caveolin-1 (cav-1) after CPZ administration. Male Wistar rats were randomly divided into two groups: a control group and a CPZ group. The CPZ group was administered CPZ intraperitoneally at a single dose of 10 mg/kg for 21 days; the controls were given the same amount of saline via the same route. On Day 22, the rats were anesthetized, and a thoracotomy was performed in all animals. Immunohistochemical analysis was performed to evaluate protein expression of E-cadherin and cav-1. Sections were analyzed by digital image analysis. Results of the present study revealed that cardiac protein expression of E-cadherin and cav-1 was altered after CPZ-induced toxicity in the rat. The expression of E-cadherin was significantly reduced, while expression of cav-1 was significantly increased after CPZ treatment, as supported by integrated optical density analysis, compared with the control (P<0.05). The current findings indicate that such changes in the expression of E-cadherin and cav-1 may be reflected in abnormal cardiac function, and these proteins may be useful in revealing the mechanisms underlying CPZ-induced toxicity and may also provide additional insight for further research.

摘要

氯丙嗪(CPZ)毒性引起的心脏损伤与各种酶和蛋白表达的变化有关。本研究旨在探讨 CPZ 给药后 CPZ 诱导的心脏 E-钙黏蛋白和小窝蛋白-1(cav-1)的改变。雄性 Wistar 大鼠随机分为两组:对照组和 CPZ 组。CPZ 组腹腔内单次给予 CPZ 10mg/kg,共 21 天;对照组给予相同剂量的生理盐水。第 22 天,麻醉大鼠,所有动物均行开胸术。进行免疫组织化学分析以评估 E-钙黏蛋白和 cav-1 的蛋白表达。通过数字图像分析对切片进行分析。本研究结果表明,CPZ 诱导的大鼠毒性后心脏 E-钙黏蛋白和 cav-1 的蛋白表达发生改变。与对照组相比(P<0.05),CPZ 处理后 E-钙黏蛋白的表达明显降低,而 cav-1 的表达明显增加,整合光密度分析支持这一结果。目前的研究结果表明,E-钙黏蛋白和 cav-1 表达的这种变化可能反映在心脏功能异常中,这些蛋白可能有助于揭示 CPZ 诱导毒性的机制,并为进一步研究提供更多的见解。

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