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首页> 外文期刊>Regulatory peptides. >Muscarinic activity modulated by C-type natriuretic peptide in gastric smooth muscles of guinea-pig stomach.
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Muscarinic activity modulated by C-type natriuretic peptide in gastric smooth muscles of guinea-pig stomach.

机译:C型利钠肽调节豚鼠胃胃平滑肌的毒蕈碱活性。

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摘要

Natriuretic peptides (NPs) are a cyclic guanosine monophosphate (cGMP) generation system like nitric oxide (NO) and play an inhibitory regulation in gastrointestinal motility but the effect of NPs on muscarinic activity is still unclear. This study was designed to investigate effect of C-type natriuretic peptide (CNP) on muscarinic control of gastric motility and its ion channel mechanism. The spontaneous contraction of gastric smooth muscle strip was recorded by using physiograph in guinea-pig. Membrane currents and potential were recorded by using whole-cell patch-clamp technique. CNP significantly inhibited muscarinic M receptor agonist carbachol (Cch)-induced contractions of gastric smooth muscle strips and dramatically hyperpolarized Cch-induced depolarization of membrane potential in gastric single smooth muscle cell. Muscarinic currents induced by both Cch and GTPgammaS, a G-protein agonist were significantly suppressed by CNP. 8-Br-cGMP mimicked the effect of CNP on Cch-induced muscarinic currents, and the peak holding current was decreased from -200.66+/-54.35 pA of control to -67.35+/-24.82 pA. LY83583, a guanylate cyclase nonspecific inhibitor, significantly weakened the inhibitory effect of CNP on muscarinic current while zaprinast, a cGMP sensitive phosphoesterase inhibitor, potentiated the inhibitory effect of CNP on muscarinic current. cGMP production was dramatically enhanced by CNP and this effect was suppressed by LY83583 in gastric smooth muscle. These results suggest that CNP modulates muscarinic activity via CNP-NPR-particulate guanylate cyclase (pGC)-cGMP pathway in guinea-pig.
机译:利钠肽(NPs)是一环鸟苷单磷酸(cGMP)生成系统,如一氧化氮(NO),在胃肠蠕动中起抑制性调控作用,但NPs对毒蕈碱活性的影响尚不清楚。本研究旨在研究C型利钠肽(CNP)对毒蕈碱控制胃动力的影响及其离子通道机制。通过生理记录仪在豚鼠中记录胃平滑肌条的自发收缩。使用全细胞膜片钳技术记录膜电流和电位。 CNP显着抑制毒蕈碱M受体激动剂卡巴胆碱(Cch)诱导的胃平滑肌条收缩,并显着超极化Cch诱导胃单平滑肌细胞膜电位去极化。由Cch和GTPgammaS(一种G蛋白激动剂)诱导的毒蕈碱电流被CNP显着抑制。 8-Br-cGMP模仿了CNP对Cch诱导的毒蕈碱电流的影响,峰值保持电流从对照组的-200.66 +/- 54.35 pA降低到-67.35 +/- 24.82 pA。鸟苷酸环化酶非特异性抑制剂LY83583显着减弱了CNP对毒蕈碱电流的抑制作用,而对cGMP敏感的磷酸酯酶抑制剂za​​prinast则增强了CNP对毒蕈碱电流的抑制作用。 CNP显着增强了cGMP的产生,而LY83583在胃平滑肌中抑制了该作用。这些结果表明,CNP通过豚鼠中的CNP-NPR-颗粒鸟苷酸环化酶(pGC)-cGMP途径调节毒蕈碱活性。

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