Larose L, Morisset J
Life Sci. 1985 Jul 22;37(3):255-61. doi: 10.1016/0024-3205(85)90651-4.
Dispersed rat pancreatic acini were incubated in 0.5mM calcium medium with increasing concentrations of carbamylcholine, with or without the ionophore A23187 (10(-6)M). Addition of the ionophore reduced maximal amylase release, increased the maximal effective concentration of carbamylcholine and dramatically impaired the agonist's capacity to induce enzyme secretion at low concentration. The ionophore also abolished the inhibition of secretion observed at high carbamylcholine concentrations. These effects of the ionophore on the cholinergic secretory response cannot be explained by interaction at the muscarinic receptor since neither the Bmax, the affinity of the receptor for the [3H]QNB nor the binding of carbamylcholine were affected by the ionophore. It is suggested that for the conditions studied, the ionophore can interact with the secretory process at one or several points ulterior to the initial recognition site of carbamylcholine on its receptor.
将分散的大鼠胰腺腺泡在含有不同浓度氨甲酰胆碱的0.5mM钙培养基中孵育,添加或不添加离子载体A23187(10^(-6)M)。添加离子载体可降低淀粉酶的最大释放量,提高氨甲酰胆碱的最大有效浓度,并显著削弱激动剂在低浓度时诱导酶分泌的能力。离子载体还消除了在高浓度氨甲酰胆碱时观察到的分泌抑制作用。离子载体对胆碱能分泌反应的这些影响不能用其与毒蕈碱受体的相互作用来解释,因为离子载体既不影响Bmax、受体对[3H]QNB的亲和力,也不影响氨甲酰胆碱的结合。研究表明,在所研究的条件下,离子载体可在氨甲酰胆碱与其受体的初始识别位点之后的一个或多个点与分泌过程相互作用。