Xue L, Farrugia G, Sarr M G, Szurszewski J H
Department of Physiology and Biophysics, Mayo Clinic, Rochester, Minnesota 55905, USA.
Am J Physiol. 1999 Jun;276(6):G1373-9. doi: 10.1152/ajpgi.1999.276.6.G1373.
The neurotransmitter(s) that generates the fast component of the inhibitory junction potential (IJP-F) in human jejunal circular smooth muscle is not known. The aim of this study was to determine the role of ATP and purinergic receptors in the generation of the IJP-F in human jejunal circular smooth muscle strips. The P2-receptor antagonist suramin (100 microM) reduced the IJP-F by 28%. Apamin (1 microM) reduced the IJP-F by 25%. Desensitization of muscle strips with the putative P2x-receptor agonist alpha, beta-methylene ATP (alpha,beta-MeATP, 100 microM) decreased the IJP-F by 44%, and desensitization with the putative P2y-receptor agonist adenosine 5'-O-2-thiodiphosphate (ADPbetaS) completely abolished the IJP-F. Desensitization with the putative P2y-receptor agonist 2-methylthioATP had no effect on the IJP-F. Exogenous ATP evoked a hyperpolarization with a time course that matched the IJP-F. The ATP-evoked hyperpolarization was reduced by apamin and suramin, reduced by desensitization with alpha,beta-MeATP (69% decrease), and abolished by desensitization with ADPbetaS. These data suggest that the IJP-F in human jejunal circular smooth muscle is mediated in part by ATP through an ADPbetaS-sensitive P2 receptor.
目前尚不清楚在人空肠环行平滑肌中产生抑制性接头电位快速成分(IJP-F)的神经递质是什么。本研究的目的是确定ATP和嘌呤能受体在人空肠环行平滑肌条IJP-F产生中的作用。P2受体拮抗剂苏拉明(100微摩尔)使IJP-F降低了28%。蜂毒明肽(1微摩尔)使IJP-F降低了25%。用假定的P2x受体激动剂α,β-亚甲基ATP(α,β-MeATP,100微摩尔)使肌条脱敏后,IJP-F降低了44%,而用假定的P2y受体激动剂5'-O-2-硫代二磷酸腺苷(ADPβS)使肌条脱敏后,IJP-F完全消失。用假定的P2y受体激动剂2-甲硫基ATP使肌条脱敏对IJP-F无影响。外源性ATP诱发的超极化的时间进程与IJP-F相符。ATP诱发的超极化被蜂毒明肽和苏拉明降低,被α,β-MeATP脱敏降低(降低69%),并被ADPβS脱敏消除。这些数据表明,人空肠环行平滑肌中的IJP-F部分是由ATP通过ADPβS敏感的P2受体介导的。