Steardo L, Iovino M, Monteleone P, Bevilacqua M, Norbiato G
Department of Neurology, 2nd Medical School, University of Naples, Italy.
J Neural Transm Gen Sect. 1990;82(3):213-7. doi: 10.1007/BF01272764.
Studies were carried out in the rat in order to investigate whether cholinergic mechanisms may be involved in vasopressin (VP) release induced by metoclopramide (MCP). The intravenous injection of MCP induced dose-related increases in plasma VP levels in water-loaded rats. These effects were prevented by atropine sulphate, but not by pirenzepine hydrochloride indicating that activation of cholinergic receptors of M-2 type was possibly required for the biologic response.
为了研究胆碱能机制是否可能参与胃复安(MCP)诱导的血管加压素(VP)释放,在大鼠身上进行了研究。给饮水负荷的大鼠静脉注射MCP会导致血浆VP水平呈剂量相关增加。这些效应被硫酸阿托品阻断,但未被盐酸哌仑西平阻断,这表明生物反应可能需要激活M-2型胆碱能受体。