Kaumann A J
Naunyn Schmiedebergs Arch Pharmacol. 1986 Apr;332(4):406-9. doi: 10.1007/BF00500096.
The role of sinoatrial beta 1- and beta 2-adrenoceptors mediating positive chronotropic effects of (-)-adrenaline and (-)-noradrenaline was investigated in rat right atria. Concentration effect curves for (-)-adrenaline, but not for (-)-noradrenaline, became biphasic in the presence of the beta 1-adrenoceptor antagonist CGP 20712 A. The curves for (-)-adrenaline in the presence of 300 nmol/l CGP 20712 A (equivalent to 1,000 times its KB, KB = 0.3 nmol/l for beta 1-adrenoceptors) comprise a high-sensitivity component that saturates at 1/4 of maximum effect, and a low sensitivity component. The high-sensitivity component is blocked by the beta 2-adrenoceptor-selective antagonist ICI 118,551. These results are consistent with an involvement in the rat of both beta 1-adrenoceptors (to a major extent) and beta 2-adrenoceptors [only at high (-)-adrenaline concentrations] in the positive chronotropic effects of (-)-adrenaline. (-)-Noradrenaline appears to activate mostly rat sinoatrial beta 1-adrenoceptors.
在大鼠右心房中研究了窦房结β1-和β2-肾上腺素能受体介导(-)-肾上腺素和(-)-去甲肾上腺素正性变时作用的作用。在β1-肾上腺素能受体拮抗剂CGP 20712 A存在的情况下,(-)-肾上腺素的浓度-效应曲线呈双相性,而(-)-去甲肾上腺素的曲线则不然。在300 nmol/l CGP 20712 A(相当于其KB的1000倍,β1-肾上腺素能受体的KB = 0.3 nmol/l)存在的情况下,(-)-肾上腺素的曲线包括一个在最大效应的1/4处饱和的高敏感性成分和一个低敏感性成分。高敏感性成分可被β2-肾上腺素能受体选择性拮抗剂ICI 118,551阻断。这些结果与β1-肾上腺素能受体(在很大程度上)和β2-肾上腺素能受体[仅在高(-)-肾上腺素浓度时]均参与(-)-肾上腺素的正性变时作用一致。(-)-去甲肾上腺素似乎主要激活大鼠窦房结β1-肾上腺素能受体。