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n-3多不饱和脂肪酸对糖尿病大鼠冠状动脉大电导钙激活钾通道蛋白表达及功能的调节作用

Regulation of Coronary Arterial Large Conductance Ca2+-Activated K+ Channel Protein Expression and Function by n-3 Polyunsaturated Fatty Acids in Diabetic Rats.

作者信息

Tang Xu, Qian Ling-Ling, Wang Ru-Xing, Yao Yong, Dang Shi-Peng, Wu Ying, Wang Wen, Ji Yuan, Sun Man-Qing, Xia Da-Yun, Liu Xiao-Yu, Zhang Dai-Min, Chai Qiang, Lu Tong

机构信息

Department of Cardiology, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, China.

出版信息

J Vasc Res. 2017;54(6):329-343. doi: 10.1159/000479870. Epub 2017 Oct 18.

Abstract

AIM

The objective of this study was to examine the effects of n-3 polyunsaturated fatty acids (n-3 PUFAs) on coronary arterial large conductance Ca2+-activated K+ (BK) channel function in coronary smooth muscle cells (SMCs) of streptozotocin-induced diabetic rats.

METHODS

The effects of docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) on coronary BK channel open probabilities were determined using the patch clamp technique. The mRNA and protein expressions of BK channel subunits were measured using qRT-PCR and Western blots. The coronary artery tension and coronary SMC Ca2+ concentrations were measured using a myograph system and fluorescence Ca2+ indicator.

RESULTS

Compared to nondiabetic control rats, the BK channel function was impaired with a reduced response to EPA and DHA in freshly isolated SMCs of diabetic rats. Oral administration of n-3 PUFAs had no effects on protein expressions of BK channel subunits in nondiabetic rats, but significantly enhanced those of BK-β1 in diabetic rats without altering BK-α protein levels. Moreover, coronary ring tension induced by iberiotoxin (a specific BK channel blocker) was increased and cytosolic Ca2+ concentrations in coronary SMCs were decreased in diabetic rats, but no changes were found in nondiabetic rats.

CONCLUSIONS

n-3 PUFAs protect the coronary BK channel function and coronary vasoreactivity in diabetic rats as a result of not only increasing BK-β1 protein expressions, but also decreasing coronary artery tension and coronary smooth muscle cytosolic Ca2+ concentrations.

摘要

目的

本研究旨在探讨n-3多不饱和脂肪酸(n-3 PUFAs)对链脲佐菌素诱导的糖尿病大鼠冠状动脉平滑肌细胞(SMCs)中冠状动脉大电导钙激活钾(BK)通道功能的影响。

方法

采用膜片钳技术测定二十二碳六烯酸(DHA)和二十碳五烯酸(EPA)对冠状动脉BK通道开放概率的影响。使用qRT-PCR和蛋白质免疫印迹法检测BK通道亚基的mRNA和蛋白质表达。使用肌张力测定系统和荧光钙指示剂测量冠状动脉张力和冠状动脉平滑肌细胞钙浓度。

结果

与非糖尿病对照大鼠相比,糖尿病大鼠新鲜分离的平滑肌细胞中BK通道功能受损,对EPA和DHA的反应降低。口服n-3 PUFAs对非糖尿病大鼠BK通道亚基的蛋白质表达无影响,但可显著提高糖尿病大鼠BK-β1的表达,而不改变BK-α蛋白水平。此外,iberiotoxin(一种特异性BK通道阻滞剂)诱导的冠状动脉环张力在糖尿病大鼠中增加,冠状动脉平滑肌细胞的胞质钙浓度降低,但在非糖尿病大鼠中未发现变化。

结论

n-3 PUFAs可保护糖尿病大鼠的冠状动脉BK通道功能和冠状动脉血管反应性,这不仅是由于增加了BK-β1蛋白表达,还降低了冠状动脉张力和冠状动脉平滑肌胞质钙浓度。

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