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Expression and alteration of BKCa channels in the sphincter of Oddi's from rabbits with hypercholesterolemia

机译:高胆固醇血症家兔Oddi括约肌中BKCa通道的表达和改变

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摘要

This study aimed to investigate the expression and function of BK_(Ca) channels in the Sphincter of Oddi (SO) in a rabbit model of hypercholesterolemia (HC). New Zealand white rabbits were randomly divided into 2 groups: the control group was fed standard chow (n = 18) whereas the high-cholesterol group was fed cholesterol-enriched chow containing 1.5% cholesterol (n = 18). The serum cholesterol level was significantly greater in the HC groups than in the control group, but there was no significant difference in body weight between the control and HC groups. Although the total protein expression of BK_(Ca) α-?and β_(1)-subunit was not significantly different between the control and HC groups, the Tyr-phosphorylation of BK_(Ca) α-subunit was significantly decreased in the HC group than in the control group. In addition, hypercholesterolemia significantly increased Acetylcholine (ACh)-induced contraction of the SO rings. Pretreatment with 30?μM NS1619, a BK_(Ca) channel agonist, significantly reduced ACh-induced contraction of the SO rings in HC rabbits. Moreover, pretreatment with 100?μM Na_(3)OV_(4), a protein tyrosine phosphatase inhibitor, significantly reduced ACh-induced contraction of the SO rings in HC rabbits, whereas it significantly increased upon pretreating with 10?μM Genistein, a tyrosine kinase inhibitor. Whole-cell patch clamp recordings showed that BK_(Ca) current density was significantly lower in SOSMCs from HC group than that from control group. Our findings suggest that hypercholesterolemia-induced downregulation of BK_(Ca) channel, and Tyr-phosphorylation of BK_(Ca) α-subunit may contribute to the hyperresponsiveness of the SO ring in HC rabbits.
机译:本研究旨在探讨高胆固醇血症(HC)兔模型中Oddi括约肌(SO)中BK_(Ca)通道的表达和功能。新西兰大白兔被随机分为2组:对照组给其喂普通食物(n = 18),而高胆固醇组给喂富含胆固醇的1.5%胆固醇食物(n = 18)。 。 HC组的血清胆固醇水平显着高于对照组,但对照组和HC组之间的体重没有显着差异。尽管对照组和HC组之间BK_(Ca)α-α和β_(1)-亚基的总蛋白表达没有显着差异,但是HC组中BK_(Ca)α-亚基的Tyr磷酸化显着降低。比对照组。此外,高胆固醇血症显着增加乙酰胆碱(ACh)诱导的SO环收缩。用BK_(Ca)通道激动剂30?μMNS1619预处理可显着降低HC兔ACh诱导的SO环收缩。此外,用蛋白质酪氨酸磷酸酶抑制剂100?μMNa_(3)OV_(4)预处理可显着降低ACh诱导的HC兔SO环收缩,而当用10?μMGenistein酪氨酸预处理时,其显着增加。激酶抑制剂。全细胞膜片钳记录显示,HC组的SOSMC中BK_(Ca)电流密度显着低于对照组。我们的发现表明,高胆固醇血症诱导的BK_(Ca)通道下调和BK_(Ca)α亚基的Tyr磷酸化可能有助于HC家兔SO环的高反应性。

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