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首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Differential participation of calcium-activated potassium channel in endothelium-dependent hyperpolarization-type relaxation in superior mesenteric arteries of spontaneously hypertensive rats
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Differential participation of calcium-activated potassium channel in endothelium-dependent hyperpolarization-type relaxation in superior mesenteric arteries of spontaneously hypertensive rats

机译:钙活化钾通道的差异参与在自发性高血压大鼠的高级肠系膜中依赖于内皮依赖性超极化型弛豫

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摘要

The purpose of this study was to determine the relationship of K-Ca channels to endothelium-dependent hyperpolarizing factor (EDHF)-mediated relaxation induced by acetylcholine (ACh) in the superior mesenteric arteries of 7-month-old spontaneously hypertensive rats (SHR). Upon inhibition of nitric oxide synthase and cyclooxygenase, ACh-induced EDHF-mediated relaxation was found to be weaker in SHR than in age-matched Wistar Kyoto rats (WKY). These relaxations in both group were attenuated by combined treatment with small-conductance and intermediate-conductance Ca2+-activated K+ channels (SKCa and IKCa) inhibitors, with the exception of relaxation resistant to inhibition of these channels in SHR (vs. WKY). Treatment with large-conductance Ca2+-activated K+ channels (BKCa) inhibitor specifically attenuated relaxation in SHR, but not in WKY. Protein expression of IKCa and SKCa in the arteries did not differ between the 2 groups, whereas ratio of slo beta 1 subunit to alpha subunit of BKCa was increased in SHR (vs. WKY). These results suggest that EDHF-mediated relaxations in superior mesenteric arteries are impaired in SHR, and utilize components of BKCa in addition to SKCa/IKCa channel activities, that the increased participation of BKCa may be attributable to alterations in alpha and slo beta 1 subunit ratio, and that components unrelated to K-Ca activity may also contribute to the difference between SHR and WKY arteries.
机译:本研究的目的是确定7月龄自发性高血压大鼠(SHR)肠系膜上动脉中K-Ca通道与乙酰胆碱(ACh)诱导的内皮依赖性超极化因子(EDHF)介导的舒张的关系。在抑制一氧化氮合酶和环氧合酶后,发现SHR中乙酰胆碱诱导的EDHF介导的舒张作用弱于年龄匹配的Wistar-Kyoto大鼠(WKY)。两组的这些舒张作用均通过小电导和中电导钙激活钾通道(SKCa和IKCa)抑制剂的联合治疗而减弱,但SHR(与WKY)对这些通道抑制的抗舒张作用除外。用大电导钙激活钾通道(BKCa)抑制剂治疗SHR可特异性地减弱舒张,但在WKY中不起作用。两组之间动脉中IKCa和SKCa的蛋白表达没有差异,而SHR中BKCa的sloβ1亚单位与α亚单位的比率增加(与WKY相比)。这些结果表明,SHR中EDHF介导的肠系膜上动脉舒张功能受损,除了SKCa/IKCa通道活性外,还利用了BKCa的成分,BKCa参与的增加可能归因于α和sloβ1亚单位比率的改变,与K-Ca活性无关的成分也可能导致SHR和WKY动脉之间的差异。

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