Robson L E, Paterson S J, Kosterlitz H W
Unit for Research on Addictive Drugs, University of Aberdeen, Marischal College, U.K.
NIDA Res Monogr. 1986;75:61-3.
NaCl, LiCl, NH4Cl and KCl inhibit the equilibrium binding of peptide agonists at each of the mu-, delta- and kappa-sites; the orders of potencies and the slopes of the dose-response curves are site-dependent. In contrast, the monovalent salt choline chloride inhibits mu- and kappa-binding but has little effect on delta-binding. The profiles of activity of MnCl2, CaCl2 and MgCl2 are also site-dependent but differ markedly from those of the monovalent salts.
氯化钠、氯化锂、氯化铵和氯化钾可抑制肽类激动剂在μ、δ和κ位点的平衡结合;效力顺序和剂量反应曲线的斜率因位点而异。相比之下,单价盐氯化胆碱可抑制μ和κ结合,但对δ结合几乎没有影响。氯化锰、氯化钙和氯化镁的活性特征也因位点而异,但与单价盐的特征明显不同。