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高血压前期自发性高血压大鼠股动脉静息状态下电压依赖性Ca++通道和Ca(++)激活的K+通道功能增强。

Increased function of voltage-dependent Ca++ channels and Ca(++)-activated K+ channels in resting state of femoral arteries from spontaneously hypertensive rats at prehypertensive stage.

作者信息

Asano M, Nomura Y, Ito K, Uyama Y, Imaizumi Y, Watanabe M

机构信息

Department of Pharmacology, Nagoya City University Medical School, Japan.

出版信息

J Pharmacol Exp Ther. 1995 Nov;275(2):775-83.

PMID:7473166
Abstract

The present study examined the possible role of voltage-dependent Ca++ channels (VDCs) and Ca(++)-activated K+ (KCa) channels in the regulation of resting tone of arteries from spontaneously hypertensive rats (SHR) at a prehypertensive stage. Differences in the effects of agents that interact with these channels were assessed in endothelium-denuded strips of femoral arteries isolated from 4-week-old SHR and age-matched normotensive Wistar-Kyoto rats (WKY). Systolic blood pressures at this age were not significantly different between SHR and WKY. The arterial strips from SHR maintained a myogenic tone in the resting state; that is the resting tone in the SHR artery was abolished when either the bathing solution was replaced with a Ca(++)-free solution or 10(-7) M nifedipine was added. Studies using 1- or 5-min pulse labeling of the arteries with 45Ca showed that the resting Ca++ influx was significantly increased in SHR when compared with WKY, and this increase in SHR was abolished by 10(-7) M nifedipine. In strips preloaded with fura-PE3, the addition of 3 x 10(-6) M verapamil to resting muscles decreased the resting cytosolic Ca++ level and caused a relaxation. These effects of verapamil were more evident in SHR than in WKY. The addition to the strips of charybdotoxin and iberiotoxin, blockers of large conductance KCa channels, caused a concentration-dependent contraction, which was significantly greater in SHR than in WKY.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究探讨了电压依赖性Ca++通道(VDCs)和Ca(++)激活的K+(KCa)通道在自发性高血压大鼠(SHR)高血压前期动脉静息张力调节中的可能作用。在从4周龄SHR和年龄匹配的正常血压Wistar-Kyoto大鼠(WKY)分离的去内皮股动脉条中,评估了与这些通道相互作用的药物的不同效应。这个年龄段SHR和WKY的收缩压没有显著差异。SHR的动脉条在静息状态下保持肌源性张力;也就是说,当用无Ca(++)溶液替换浴液或加入10(-7) M硝苯地平时,SHR动脉的静息张力消失。用45Ca对动脉进行1或5分钟脉冲标记的研究表明,与WKY相比,SHR的静息Ca++内流显著增加,而SHR中的这种增加被10(-7) M硝苯地平消除。在预先加载fura-PE3的条带中,向静息肌肉中加入3×10(-6) M维拉帕米可降低静息胞质Ca++水平并引起舒张。维拉帕米的这些作用在SHR中比在WKY中更明显。向条带中加入大电导KCa通道阻滞剂蝎毒素和iberiotoxin会引起浓度依赖性收缩,这种收缩在SHR中比在WKY中显著更大。(摘要截断于250字)

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