Saito K, Potter W Z, Saavedra J M
Unit of Preclinical Neuropharmacology, National Institute of Mental Health, Bethesda, MD 20892.
Eur J Pharmacol. 1988 Aug 24;153(2-3):289-93. doi: 10.1016/0014-2999(88)90617-6.
We studied beta-adrenoceptors by quantitative autoradiography in the cardiac vagus ganglia of the rat, after incubation of tissue sections with [125I]iodocyanopindolol. The cardiac vagus ganglia presented a high concentration of a single population of high affinity binding sites (Bmax 109 +/- 10 fmol/mg protein; Kd 64 +/- 5 pM). Displacement studies with the beta 1-selective adrenoceptor antagonist CGP 20712 A and the beta 2-selective adrenoceptor antagonist ICI 118,551 indicated that most (80 to 90%) of the binding sites are of the beta 2-type.
在用[125I]碘氰吲哚洛尔孵育组织切片后,我们通过定量放射自显影术研究了大鼠心脏迷走神经节中的β-肾上腺素能受体。心脏迷走神经节呈现出单一高亲和力结合位点群体的高浓度(Bmax为109±10 fmol/mg蛋白质;Kd为64±5 pM)。用β1选择性肾上腺素能受体拮抗剂CGP 20712 A和β2选择性肾上腺素能受体拮抗剂ICI 118,551进行的置换研究表明,大多数(80%至90%)结合位点为β2型。