Griessen M
Gastroenterology. 1978 Feb;74(2 Pt 1):263-70.
Guanylate cyclase in the guinea pig fundic mucosa occurred in two enzymatic forms: a "soluble" form and a particulate form. The mean basal activity of the soluble fraction measured in the presence of 300 micrometer guanosine-5'-triphosphate and 5 mM MnCl2 was 72.6 +/- 5.3 pmoles of cyclic GMP per mg of protein per min. Guanylate cyclase activity was dependent on Mn2+; it was increased by sodium azide (NaN3), CaCl2, cysteine, secretin, and cholecystokinin, but it was not influenced by gastrin, histamine, cholinergic esters, prostaglandins E1 and A1. NaN3 (1 mM) decreased the apparent Km for MnCl2 and potentiated the effects of MgCl2. The activity of the particulate fraction represented about 14% of that of the supernatant fraction. The guanylate cyclase activity of that fraction was not modified by NaN3, gastrin, cholinergic agents, secretin, or cholecystokinin. Cysteine inhibited its activity. These data do not support the hypothesis that cyclic GMP acts as a second messenger for the action of cholinergic agents and gastrin in the guinea pig gastric mucosa.
一种“可溶性”形式和一种颗粒形式。在300微摩尔鸟苷-5'-三磷酸和5毫摩尔氯化锰存在下测得的可溶性部分的平均基础活性为每分钟每毫克蛋白质72.6±5.3皮摩尔环磷酸鸟苷。鸟苷酸环化酶活性依赖于锰离子;它可被叠氮化钠(NaN₃)、氯化钙、半胱氨酸、促胰液素和胆囊收缩素增强,但不受胃泌素、组胺、胆碱酯、前列腺素E₁和A₁影响。1毫摩尔的NaN₃降低了对氯化锰的表观米氏常数,并增强了氯化镁的作用。颗粒部分的活性约为上清液部分活性的14%。该部分的鸟苷酸环化酶活性不受NaN₃、胃泌素、胆碱能药物、促胰液素或胆囊收缩素的影响。半胱氨酸抑制其活性。这些数据不支持环磷酸鸟苷作为胆碱能药物和胃泌素在豚鼠胃黏膜中作用的第二信使这一假说。