Kaumann A J, Birnbaumer L
Naunyn Schmiedebergs Arch Pharmacol. 1976 May;293(2):199-202. doi: 10.1007/BF00499230.
Desensitization of kitten atria with 30muM (-)isoprenaline resulted in a 6-fold and 15-fold increase in the EC50's of (-)isoprenaline for its positive chronotropic effects (sinus pacemakers) and positive inotropic effects (left atria), respectively, but only in a 2-fold increase of the EC50 of (-)isoprenaline for adenylyl cyclase stimulation in membrane particles from atria. However, maximum cyclase stimulation by (-)isoprenaline was decreased to 1/2 in membranes from (-)isoprenaline-treated atria, whereas maximum increases in rate of sinus pacemakers and force of left atria were unchanged and reduced by 15%, respectively. The high affinity beta-adrenoceptor blocker (-)bupranolol antagonized the adenylyl cyclase stimulation by (-)isoprenaline to similar extent in membranes from (-)isoprenaline and untreated atria, suggesting that the apparent affinity of beta-adrenoceptors for ligands is unchanged by desensitization. The evidence is compatible with the concept that desensitization is associated with decreased availability of receptors and with the view that near maximal positive chronotropic effects of catecholamines may be caused by only threshold increases in membrane adenylyl cyclase activity.
用30μM(-)异丙肾上腺素对小猫心房进行脱敏处理后,(-)异丙肾上腺素对其正性变时作用(窦房结起搏点)和正性变力作用(左心房)的半数有效浓度(EC50)分别增加了6倍和15倍,但对心房膜颗粒中腺苷酸环化酶刺激作用的(-)异丙肾上腺素EC50仅增加了2倍。然而,(-)异丙肾上腺素处理过的心房膜中,(-)异丙肾上腺素对环化酶的最大刺激作用降至未处理时的1/2,而窦房结起搏点速率的最大增加和左心房力量的最大增加分别未改变和降低了15%。高亲和力β-肾上腺素能受体阻滞剂(-)布普萘洛尔在(-)异丙肾上腺素处理过的心房膜和未处理的心房膜中,对(-)异丙肾上腺素刺激腺苷酸环化酶的拮抗作用程度相似,这表明脱敏并未改变β-肾上腺素能受体对配体的表观亲和力。该证据与脱敏与受体可利用性降低相关的概念相符,也与儿茶酚胺接近最大正性变时作用可能仅由膜腺苷酸环化酶活性阈值升高引起的观点相符。