Michel M C, Philipp T, Brodde O E
Department of Internal Medicine, University of Essen, Germany.
Pharmacol Toxicol. 1992 Jun;70(6 Pt 2):S1-10. doi: 10.1111/j.1600-0773.1992.tb01615.x.
Recent years have witnessed astonishing progress in our understanding of the molecular basis of adrenoceptor structure, function and regulation and revealed an unexpected heterogeneity of adrenoceptors demonstrating the existence of at least 11 subtypes. This paper discusses the implications of these advances on studies regarding a specific role of adrenoceptors in the development of genetic hypertension. The available data indicate that among the alpha-adrenoceptor subtypes the alpha 2A-adrenoceptor is the most likely candidate for an alteration specifically linked to genetic hypertension in the animal model of the spontaneously hypertensive rat and possibly in some patients. Alterations of other alpha-adrenoceptor subtypes may be specific for some forms of genetic hypertension but are unlikely to play an important role for blood pressure regulation. Most beta-adrenoceptor alterations appear to occur secondary to blood pressure elevation independently of whether hypertension has occurred on a genetic basis or not. Moreover, the mechanisms regulating alpha- and beta-adrenoceptor responsiveness upon prolonged agonist exposure may be altered in hypertension and thereby contribute to the pathophysiology of this disease.
近年来,我们对肾上腺素能受体的结构、功能及调节的分子基础的理解取得了惊人进展,并且揭示了肾上腺素能受体出人意料的异质性,这表明至少存在11种亚型。本文讨论了这些进展对于肾上腺素能受体在遗传性高血压发生中特定作用研究的意义。现有数据表明,在α-肾上腺素能受体亚型中,α2A-肾上腺素能受体最有可能是与自发性高血压大鼠动物模型以及可能某些患者的遗传性高血压特别相关的改变的候选者。其他α-肾上腺素能受体亚型的改变可能对某些形式的遗传性高血压具有特异性,但不太可能在血压调节中起重要作用。大多数β-肾上腺素能受体改变似乎是血压升高的继发结果,无论高血压是否基于遗传发生。此外,在高血压中,长时间激动剂暴露后调节α-和β-肾上腺素能受体反应性的机制可能会改变,从而促成该疾病的病理生理学。