Fisher S K, Slowiejko D M, McEwen E L
Department of Pharmacology, University of Michigan Ann Arbor 48104-1687.
Neurochem Res. 1994 May;19(5):549-54. doi: 10.1007/BF00971329.
Agonist occupancy of muscarinic cholinergic receptors in human SH-SY-5Y neuroblastoma cells elicited two kinetically distinct phases of phosphoinositide hydrolysis when monitored by either an increased mass of inositol 1,4,5-trisphosphate, or the accumulation of a total inositol phosphate fraction. Within 5s of the addition of the muscarinic agonist, oxotremorine-M, the phosphoinositide pool was hydrolyzed at a maximal rate of 9.5%/min. This initial phase of phosphoinositide hydrolysis was short-lived (t1/2 = 14s) and after 60s of agonist exposure, the rate of inositol lipid breakdown had declined to a steady state level of 3.4%/min which was then maintained for at least 5-10 min. This rapid, but partial, attenuation of muscarinic receptor stimulated phosphoinositide hydrolysis occurred prior to the agonist-induced internalization of muscarinic receptors.
当通过增加的1,4,5-三磷酸肌醇量或总磷酸肌醇部分的积累进行监测时,毒蕈碱胆碱能受体的激动剂占据人SH-SY-5Y神经母细胞瘤细胞会引发两个动力学上不同的磷酸肌醇水解阶段。在添加毒蕈碱激动剂氧化震颤素-M后的5秒内,磷酸肌醇池以9.5%/分钟的最大速率水解。磷酸肌醇水解的这个初始阶段是短暂的(半衰期=14秒),在激动剂暴露60秒后,肌醇脂质分解速率已降至3.4%/分钟的稳态水平,然后维持至少5-10分钟。毒蕈碱受体刺激的磷酸肌醇水解的这种快速但部分的衰减发生在激动剂诱导的毒蕈碱受体内化之前。