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首页> 外文期刊>Japanese Journal of Pharmacology >The Mechanism of Muscarinic Agonist-Stimulated Inositol Phosphate Formation in Permeabilized Ileal Smooth Muscle
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The Mechanism of Muscarinic Agonist-Stimulated Inositol Phosphate Formation in Permeabilized Ileal Smooth Muscle

机译:毒蕈碱激动剂刺激肌钙蛋白在平滑肌回肠平滑肌中形成的机理

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References(26) Cited-By(1) Muscarinic agonists and guanylyl-5''-imidodiphosphate (Gpp(NH)p) stimulated formation of inositol phosphates in permeabilized longitudinal smooth muscle of guinea pig ileum. Gpp(NH)p markedly potentiated the formation of inositol bisphosphate (IP2) and inositol trisphosphate (IP3) stimulated by carbachol, but increased inositol monophosphate formation (IP1) only slightly. Gpp(NH)p enhanced the formation of IP2 + IP3 induced by either acetylcholine or carbachol about fourfold in a synergistic manner, but enhanced the effects of oxotremorine and pilocarpine less than twofold in an additive manner. Elevation of Ca2+ concentration resulted in increases of the inositol phosphate levels stimulated by both carbachol and Gpp(NH)p. The optimal concentration of Ca2+ for carbachol-stimulated formations of IP2 + IP3 was shifted to a lower Ca2+ concentration in the presence of Gpp(NH)p. These findings suggest that muscarinic receptor-stimulated polyphosphoinositide hydrolysis in ileal smooth muscle results in inositol polyphosphate formation via GTP binding protein (G-protein). The muscarinic receptor-activated G-protein decreases the Ca2+ requirement of polyphosphoinositide hydrolysis. Muscarinic agonists stimulate inositol polyphosphate formation by interaction of the G-protein activation of a phosphoinositide specific phospholipase C with Ca2+ influx.
机译:参考文献(26)被引用的By(1)毒蕈碱激动剂和鸟苷基5''-亚氨基二磷酸(Gpp(NH)p)刺激了豚鼠回肠通透性纵向平滑肌中肌醇磷酸酯的形成。 Gpp(NH)p显着增强了卡巴胆碱刺激的肌醇二磷酸酯(IP2)和肌醇三磷酸酯(IP3)的形成,但仅略微增加了肌醇单磷酸酯的形成(IP1)。 Gpp(NH)p以协同方式将乙酰胆碱或卡巴胆碱诱导的IP2 + IP3的形成提高了约4倍,但以加性方式将氧代雷莫林和毛果芸香碱的作用增强了不到2倍。 Ca2 +浓度的升高会导致碳酰胆碱和Gpp(NH)p刺激的肌醇磷酸水平升高。在存在Gpp(NH)p的情况下,由卡巴胆碱刺激的IP2 + IP3形成的最佳Ca2 +浓度转移到较低的Ca2 +浓度。这些发现表明,回肠平滑肌中毒蕈碱受体刺激的聚磷酸肌醇水解会通过GTP结合蛋白(G蛋白)形成肌醇多磷酸盐。毒蕈碱受体激活的G蛋白降低了多磷酸肌醇水解的Ca2 +需求。毒蕈碱激动剂通过磷酸肌醇特异性磷脂酶C的G蛋白活化与Ca2 +内流相互作用,刺激肌醇多磷酸盐的形成。

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