Ogishima M, Kaibara M, Ueki S, Kurimoto T, Taniyama K
Department of Pharmacology, Nagasaki University School of Medicine, Nagasaki, Japan.
J Pharmacol Exp Ther. 2000 Jul;294(1):33-7.
The mechanism by which Z-338, a novel gastroprokinetic agent, stimulates gastric motility was studied in relation to muscarinic receptors in the guinea pig. Z-338 (3-30 microM) enhanced electrically stimulated contractions and the release of acetylcholine (ACh) that was tetrodotoxin sensitive and extracellular Ca(2+) dependent, in gastric strips. Membrane-binding assay revealed that Z-338 possessed binding affinity for muscarinic M(1) and M(2), but not M(3) receptors. In Xenopus oocytes expressing M(1) and M(2) muscarinic receptors, Z-338 did not produce any response, but inhibited ACh-induced outward currents, thereby indicating that Z-338 acts on the M(1) and M(2) muscarinic receptors as an antagonist. The M(1) receptor antagonist pirenzepine (0.5 microM) and M(2) receptor antagonist AF-DX 116 (1 microM) also enhanced electrically stimulated release of ACh. These results indicate that Z-338 facilitates ACh release from cholinergic nerve terminals by blocking muscarinic M(1) and M(2) autoreceptors, which regulate the release of ACh.
研究了新型促胃动力药Z-338刺激豚鼠胃动力的机制与毒蕈碱受体的关系。Z-338(3-30微摩尔)增强了胃条带中电刺激引起的收缩以及乙酰胆碱(ACh)的释放,该释放对河豚毒素敏感且依赖细胞外Ca(2+)。膜结合试验表明,Z-338对毒蕈碱M(1)和M(2)受体具有结合亲和力,但对M(3)受体没有。在表达M(1)和M(2)毒蕈碱受体的非洲爪蟾卵母细胞中,Z-338未产生任何反应,但抑制了ACh诱导的外向电流,从而表明Z-338作为拮抗剂作用于M(1)和M(2)毒蕈碱受体。M(1)受体拮抗剂哌仑西平(0.5微摩尔)和M(2)受体拮抗剂AF-DX 116(1微摩尔)也增强了电刺激引起的ACh释放。这些结果表明,Z-338通过阻断调节ACh释放的毒蕈碱M(1)和M(2)自身受体来促进胆碱能神经末梢释放ACh。