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氯沙坦对兔动脉粥样硬化早期连接蛋白表达的影响。

Effects of Losartan on expression of connexins at the early stage of atherosclerosis in rabbits.

机构信息

The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, China.

出版信息

Int J Med Sci. 2010 May 8;7(2):82-9. doi: 10.7150/ijms.7.82.

Abstract

AIM

to investigate effects of Losartan on expression of connexin 40 and 43 (Cx40 and Cx43), in arteries at the early stage of atherosclerosis in a rabbit model.

METHODS

A total of 28 male New Zealand white rabbits were divided into following groups: control group, high fat diet group, and Losartan group (10 mg/kg/day). Losartan was administrated in food for two weeks. Iliac arteries were obtained for immunohistochemistry, transmission electron microscopy, Western blot, and reverse transcriptase-polymerase chain reaction (RT-PCR).

RESULTS

Transmission electron microscopy revealed abundant gap junctions between neointimal smooth muscle cells (SMCs), which were markedly reduced by treatment. RT-PCR and Western blot assay showed that the mRNA and protein expression of Cx40 and Cx43 were elevated in the neointimal area at the early stage of atherosclerosis. The mRNA and protein expression of Cx43 were significantly down-regulated by losartan treatment but those of Cx40 were not markedly changed.

CONCLUSION

Cx40 and Cx43 in the neointimal SMCs were up-regulated at the early stage of atherosclerosis. Losartan (an angiotensin-converting enzyme inhibitor) could reduce neointima proliferation and down-regulate the elevated protein expression of Cx43, suggesting the rennin-angiotensin system (RAS) plays an important role in the remodeling of gap junction between ventricular myocytes under pathological conditions.

摘要

目的

研究氯沙坦对兔动脉粥样硬化早期缝隙连接蛋白 40 和 43(Cx40 和 Cx43)表达的影响。

方法

将 28 只雄性新西兰白兔分为对照组、高脂饮食组和氯沙坦组(10mg/kg/天)。氯沙坦通过食物给药 2 周。取髂动脉进行免疫组织化学、透射电镜、Western blot 和逆转录-聚合酶链反应(RT-PCR)检测。

结果

透射电镜显示,新生内膜平滑肌细胞(SMCs)之间存在丰富的缝隙连接,经治疗后明显减少。RT-PCR 和 Western blot 检测显示,动脉粥样硬化早期新生内膜区 Cx40 和 Cx43 的 mRNA 和蛋白表达增加。氯沙坦治疗后 Cx43 的 mRNA 和蛋白表达显著下调,但 Cx40 的表达无明显变化。

结论

动脉粥样硬化早期新生内膜 SMC 中的 Cx40 和 Cx43 表达上调。血管紧张素转换酶抑制剂氯沙坦可减少新生内膜增殖,并下调 Cx43 的高表达,提示在病理条件下,肾素-血管紧张素系统(RAS)在心室肌细胞缝隙连接重构中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49f1/2869452/4a662a3cdc57/ijmsv07p0082g01.jpg

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