Waldman S A, Rapoport R M, Fiscus R R, Murad F
Biochim Biophys Acta. 1985 May 30;845(2):298-303. doi: 10.1016/0167-4889(85)90191-0.
Atriopeptin II activated particulate guanylate cyclase 5-10-fold in a concentration- and time-dependent fashion in crude membranes obtained from homogenates of rat adrenal cortex or medulla. Similar effects were observed with other atriopeptin analogs. Soluble guanylate cyclase and adenylate cyclase in these preparations were not activated. Accumulation of cyclic GMP in minces of adrenal cortex or medulla was increased 6-8-fold due to atriopeptin II activation of particulate guanylate cyclase. Several thiol-reactive agents blocked the activation of particulate guanylate cyclase, suggesting that free thiol groups on membrane proteins may be important in atriopeptin receptor-guanylate cyclase coupling.
心房肽II能使从大鼠肾上腺皮质或髓质匀浆中获得的粗制膜中的颗粒型鸟苷酸环化酶以浓度和时间依赖性方式激活5到10倍。其他心房肽类似物也观察到类似效果。这些制剂中的可溶性鸟苷酸环化酶和腺苷酸环化酶未被激活。由于心房肽II激活颗粒型鸟苷酸环化酶,肾上腺皮质或髓质碎块中环状GMP的积累增加了6到8倍。几种硫醇反应性试剂阻断了颗粒型鸟苷酸环化酶的激活,这表明膜蛋白上的游离硫醇基团在心房肽受体-鸟苷酸环化酶偶联中可能很重要。