Honda K, Takano Y, Kamiya H
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.
Jpn J Pharmacol. 1994 Jul;65(3):275-80. doi: 10.1254/jjp.65.275.
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.
毒蕈碱激动剂和鸟苷 - 5'-亚氨基二磷酸(Gpp(NH)p)可刺激豚鼠回肠纵行平滑肌中通透细胞内肌醇磷酸的形成。Gpp(NH)p显著增强了卡巴胆碱刺激的肌醇二磷酸(IP2)和肌醇三磷酸(IP3)的形成,但仅轻微增加了肌醇单磷酸(IP1)的形成。Gpp(NH)p以协同方式使乙酰胆碱或卡巴胆碱诱导的IP2 + IP3形成增加约四倍,但以相加方式使氧化震颤素和毛果芸香碱的作用增强不到两倍。Ca2+浓度升高导致卡巴胆碱和Gpp(NH)p刺激的肌醇磷酸水平增加。在存在Gpp(NH)p的情况下,卡巴胆碱刺激IP2 + IP3形成的最佳Ca2+浓度移至较低的Ca2+浓度。这些发现表明,毒蕈碱受体刺激的回肠平滑肌中多磷酸肌醇水解通过GTP结合蛋白(G蛋白)导致肌醇多磷酸形成。毒蕈碱受体激活的G蛋白降低了多磷酸肌醇水解对Ca2+的需求。毒蕈碱激动剂通过磷酸肌醇特异性磷脂酶C的G蛋白激活与Ca2+内流的相互作用刺激肌醇多磷酸的形成。