Goodhardt M, Ferry N, Aggerbeck M, Hanoune J
Biochem Pharmacol. 1984 Mar 15;33(6):863-8. doi: 10.1016/0006-2952(84)90439-8.
Since the relatively recent advent of radioligand binding techniques, it has been possible to directly identify and characterize hepatic adrenergic receptors as well as study their physiological regulation. While it is now clear that alpha 1-adrenergic receptors constitute the major population of hepatic adrenergic receptors and are primarily responsible for the actions of catecholamines in liver, relatively little is known about the molecular mechanisms underlying alpha 1-responses. Recent results suggest that guanine nucleotides may be implicated in the transmission of the hormonal signal from the hepatic alpha 1-receptor to its effectors in a manner analogous to that described for adenylate cyclase-linked receptors. The lack of an easily measurable proximal membrane response for the alpha 1-receptor has been a severe handicap in our understanding of the mechanism of transmission of the hormonal signal. It is likely that until such a response is defined, alpha 1-adrenergic research will continue to lag behind research on the beta-adrenergic receptor.
自从放射性配体结合技术相对较新出现以来,人们已经能够直接鉴定和表征肝脏肾上腺素能受体,并研究其生理调节。虽然现在很清楚α1肾上腺素能受体构成了肝脏肾上腺素能受体的主要群体,并且主要负责儿茶酚胺在肝脏中的作用,但对于α1反应背后的分子机制了解相对较少。最近的结果表明,鸟嘌呤核苷酸可能以类似于腺苷酸环化酶偶联受体所描述的方式参与激素信号从肝脏α1受体向其效应器的传递。缺乏易于测量的α1受体近端膜反应一直是我们理解激素信号传递机制的严重障碍。很可能在定义出这样一种反应之前,α1肾上腺素能研究将继续落后于β肾上腺素能受体的研究。