Yau W M, Dorsett J A, Youther M L
Department of Medical Physiology and Pharmacology, School of Medicine, Southern Illinois University, Carbondale.
J Pharmacol Exp Ther. 1987 Nov;243(2):507-10.
Forskolin, an activator of adenylate cyclase, was used to examine the regulation of [3H]acetylcholine (ACh) release by cyclic AMP (cAMP)-related mechanisms in myenteric plexus-longitudinal muscle preparations of guinea pig small intestine. Forskolin evoked a dose-related increase in [3H]ACh release. Both dibutyryl-cAMP and 8-Br-cAMP significantly elevated [3H]ACh secretion. In the presence of phosphodiesterase inhibitors (theophylline and 3-isobutyl-1-methylxanthine), the basal [3H]ACh output was increased. There was a significantly greater stimulation when forskolin was used to incite endogenous cAMP synthesis and phosphodiesterase inhibitors were simultaneously applied to prevent cAMP breakdown. The enhancement of forskolin-stimulated release by theophylline or 3-isobutyl-1-methylxanthine strongly implicates a synergistic interaction between the two. These findings suggest that forskolin acts to increase ACh release by a modulation of endogenous cAMP and further support a cAMP-mediated mechanism in the secretion of ACh from myenteric cholinergic neurons.
毛喉素是一种腺苷酸环化酶激活剂,被用于研究豚鼠小肠肌间神经丛-纵肌标本中,环磷酸腺苷(cAMP)相关机制对[3H]乙酰胆碱(ACh)释放的调节作用。毛喉素引起[3H]ACh释放呈剂量相关增加。二丁酰-cAMP和8-溴-cAMP均显著提高[3H]ACh分泌。在磷酸二酯酶抑制剂(茶碱和3-异丁基-1-甲基黄嘌呤)存在的情况下,基础[3H]ACh输出增加。当使用毛喉素激发内源性cAMP合成并同时应用磷酸二酯酶抑制剂以防止cAMP分解时,刺激作用显著增强。茶碱或3-异丁基-1-甲基黄嘌呤对毛喉素刺激释放的增强作用强烈表明两者之间存在协同相互作用。这些发现表明,毛喉素通过调节内源性cAMP来增加ACh释放,并进一步支持cAMP介导的肌间胆碱能神经元释放ACh的机制。