Reinhardt R R, Roskoski R
J Pharmacol Exp Ther. 1983 Jul;226(1):135-9.
The regulation of the muscarinic receptor by the agonist methacholine was investigated in the perfused working rat heart. After 2.5 hr of perfusion with 4 microM methacholine, the number of (-)-[3H]-quinuclidinyl benzilate binding sites was significantly reduced (10-18%) in the right and left atria and left ventricle when compared with controls (2.5 hr of perfusion in the absence of methacholine). Scatchard analysis revealed that there was no change in the apparent dissociation constant for quinuclidinyl benzilate. Furthermore, when hearts were perfused for 2.5 hr with methacholine in the presence of (-)-scopolamine, a muscarinic receptor antagonist, no significant loss of receptor was observed. After perfusing with methacholine for 2.5 hr followed by 2.5 hr in the absence of agonist, the number of quinuclidinyl benzilate binding sites returned to control levels. These results suggest that agonist-induced receptor decreases or down regulation requires receptor activation and not just simple receptor occupancy. This decrease, moreover, is reversible. The perfused working rat heart represents a physiological system in which the mechanisms of muscarinic receptor regulation can be studied.
在灌注的工作大鼠心脏中研究了激动剂乙酰甲胆碱对毒蕈碱受体的调节作用。在用4μM乙酰甲胆碱灌注2.5小时后,与对照组(在无乙酰甲胆碱的情况下灌注2.5小时)相比,右心房、左心房和左心室中(-)-[3H]-奎宁环基苯甲酸酯结合位点的数量显著减少(10 - 18%)。Scatchard分析表明,奎宁环基苯甲酸酯的表观解离常数没有变化。此外,当心脏在毒蕈碱受体拮抗剂(-)-东莨菪碱存在的情况下用乙酰甲胆碱灌注2.5小时时,未观察到受体的显著损失。在用乙酰甲胆碱灌注2.5小时后,再在无激动剂的情况下灌注2.5小时,奎宁环基苯甲酸酯结合位点的数量恢复到对照水平。这些结果表明,激动剂诱导的受体减少或下调需要受体激活,而不仅仅是简单的受体占据。此外,这种减少是可逆的。灌注的工作大鼠心脏代表了一个可以研究毒蕈碱受体调节机制的生理系统。