Ward D, Young J M
Br J Pharmacol. 1977 Oct;61(2):189-97. doi: 10.1111/j.1476-5381.1977.tb08404.x.
1 The binding of ligands to muscarinic receptors in intact longitudinal muscle strips from guinea-pig small intestine has been determined by measuring the inhibition of the irreversible binding of [3H]-propylbenzilylcholine mustard ([3H]-PrBCM). 2 The IC50 values for inhibition of [3H]-PrBCM binding by a given ligand were generally higher in intact strips than those reported for broken-cell preparations. This effect is probably due, at least in part, to the presence of an access-limitation factor in the kinetics of the irreversible binding of [3H]-PrBCM to the intact tissue. 3 The mean Hill coefficients for antagonist binding approached unity, but those for strong agonists were significantly less than unity. There was, with the possible exceptions of hexyltrimethylammonium and oxotremorine, reasonably good agreement with the Hill coefficients reported for brain homogenates.
1 通过测量[3H]-丙基苄基胆碱氮芥([3H]-PrBCM)不可逆结合的抑制作用,已确定了配体与豚鼠小肠完整纵肌条中毒蕈碱受体的结合情况。2 给定配体对[3H]-PrBCM结合的抑制作用的IC50值在完整肌条中通常高于破碎细胞制剂中报道的值。这种效应至少部分可能是由于[3H]-PrBCM与完整组织不可逆结合动力学中存在进入限制因子。3 拮抗剂结合的平均希尔系数接近1,但强激动剂的希尔系数明显小于1。除己基三甲基铵和氧化震颤素可能例外,与脑匀浆中报道的希尔系数有较好的一致性。