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α和β肾上腺素能受体阻滞剂在抗高血压治疗中的作用。

The role of alpha- and beta-adrenoceptor blockade in antihypertensive treatment.

作者信息

van Zwieten P A

机构信息

Department of Pharmacotherapy, University of Amsterdam.

出版信息

Clin Investig. 1992;70 Suppl 1:S7-12. doi: 10.1007/BF00207605.

Abstract

The alpha and beta-adrenoceptors are at present subdivided into alpha 1/alpha 2 and beta 1/beta 2 (probably also beta 3) subtypes. This subdivision, based on functional pharmacological studies, has been largely confirmed by molecular biological techniques. At presynaptic sites alpha 2- and beta 2-adrenoceptors are known to predominate, whereas both alpha 1/alpha 2- and beta 1/beta 2-receptors may be found at postsynaptic sites. This subdivision and classification of adrenoceptors, receptor changes in disease, and the availability of agonists and antagonists for the various receptor subtypes are discussed as the basis for antihypertensive drug therapy. alpha-Adrenoceptor antagonists are vasodilators, which owe their antihypertensive activity to arterial vasodilatation, while venous dilatation occurs simultaneously. Selective alpha 1-antagonists (prazosin, doxazosin) are preferable to the older nonselective compounds like phentolamine. beta-Blockers are useful antihypertensive agents used on a very large scale, but their mode of action remains unknown in detail. The combination of alpha- and beta-adrenoceptor blockade would be attractive, particularly for hemodynamic reasons. alpha-Adrenoceptor blockade reduces peripheral vascular resistance but also counteracts the vasoconstrictor effect of beta-blockers in the extremities, underlying the well-known side-effect of cold hands and feet. beta-Adrenoceptor blockade will not only contribute to the hypotensive effect but also suppress reflex tachycardia induced by alpha-adrenoceptor blockade.

摘要

目前,α和β肾上腺素能受体可细分为α1/α2和β1/β2(可能还有β3)亚型。这种基于功能药理学研究的细分在很大程度上已得到分子生物学技术的证实。已知在突触前部位以α2和β2肾上腺素能受体为主,而在突触后部位则可发现α1/α2和β1/β2受体。本文讨论了肾上腺素能受体的这种细分和分类、疾病中的受体变化以及针对各种受体亚型的激动剂和拮抗剂的可用性,作为抗高血压药物治疗的基础。α肾上腺素能受体拮抗剂是血管扩张剂,其抗高血压活性归因于动脉血管扩张,同时伴有静脉扩张。选择性α1拮抗剂(哌唑嗪、多沙唑嗪)优于酚妥拉明等较老的非选择性化合物。β受体阻滞剂是广泛使用的有用抗高血压药物,但其详细作用方式仍不清楚。α和β肾上腺素能受体阻滞剂联合使用可能很有吸引力,特别是从血流动力学角度来看。α肾上腺素能受体阻滞剂可降低外周血管阻力,但也可抵消β受体阻滞剂在四肢的血管收缩作用,这是众所周知的手脚冰凉副作用的原因。β肾上腺素能受体阻滞剂不仅有助于降压,还可抑制α肾上腺素能受体阻滞剂引起的反射性心动过速。

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