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首页> 外文期刊>Physiological Research >The effect of C-type natriuretic peptide on delayed rectifier potassium currents in gastric antral circular myocytes of the guinea-pig
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The effect of C-type natriuretic peptide on delayed rectifier potassium currents in gastric antral circular myocytes of the guinea-pig

机译:C型利钠肽对豚鼠胃窦胃环形肌细胞延迟整流钾电流的影响

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C-type natriuretic peptides (CNP) play an inhibitory role in smooth muscle motility of the gastrointestinal tract, but the effect of CNP on delayed rectifier potassium currents is still unclear. This study was designed to investigate the effect of CNP on delayed rectifier potassium currents and its mechanism by using conventional whole-cell patch-clamp technique in guinea-pig gastric myocytes isolated by collagenase. CNP significantly inhibited delayed rectifier potassium currents [I-K (v)] in dose-dependent manner, and CNP inhibited the peak current elicited by depolarized step pulse to 86.1 +/- 1.6 % (n=7, P<0.05), 78.4 +/- 2.6 % (n=10, P<0.01) and 67.7 +/- 2.3 % (n=14, P<0.01), at concentrations of 0.01 mu mol/l, 0.1 mu mol/l and 1 mu mol/l, respectively, at +60 mV. When the cells were preincubated with 0.1 mu mol/l LY83583, a guanylate cyclase inhibitor, the 1 mu mol/l CNP-induced inhibition of I-K (v) was significantly impaired but when the cells were preincubated with 0.1 mu mol/l zaprinast, a cGMP-sensitive phosphodiesterase inhibitor, the 0.01 mu mol/l CNP-induced inhibition of I-K (v) was significantly potentiated. 8-Br-cGMP, a membrane permeable cGMP analogue mimicked inhibitory effect of CNP on I-K (v). CNP-induced inhibition of I-K (v) was completely blocked by KT5823, an inhibitor of cGMP-dependent protein kinase (PKG). The results suggest that CNP inhibites the delayed rectifier potassium currents via cGMP-PKG signal pathway in the gastric antral circular myocytes of the guinea-pig.
机译:C型利钠肽(CNP)在胃肠道平滑肌运动中起抑制作用,但CNP对延迟整流钾电流的影响尚不清楚。本研究旨在通过使用常规全细胞膜片钳技术研究CNP对延迟胶原蛋白分离的豚鼠胃肌细胞的影响及其机制。 CNP以剂量依赖性方式显着抑制延迟整流器钾电流[IK(v)],并且CNP将去极化步进脉冲引起的峰值电流抑制为86.1 +/- 1.6%(n = 7,P <0.05),78.4 + / -浓度为0.01μmol / l,0.1μmol / l和1μmol / l时为2.6%(n = 10,P <0.01)和67.7 +/- 2.3%(n = 14,P <0.01),分别为+60 mV。当将细胞与鸟苷酸环化酶抑制剂0.1μmol/ l LY83583预温育时,1μmol/ l CNP诱导的IK(v)抑制作用显着减弱,但是当将细胞与0.1μmol/ l zaprinast预温育时,作为cGMP敏感的磷酸二酯酶抑制剂,0.01μmol / l CNP诱导的IK(v)抑制作用显着增强。 8-Br-cGMP,一种膜渗透性cGMP类似物,模仿了CNP对I-K的抑制作用(v)。 CNP诱导的I-K(v)抑制作用被cGMP依赖性蛋白激酶(PKG)抑制剂KT5823完全阻断。结果表明,CNP通过cGMP-PKG信号通路抑制豚鼠胃窦圆形肌细胞中的延迟整流钾电流。

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