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β受体阻滞剂的脑内水平及急性降压活性

Brain levels and acute antihypertensive activity of beta-blockers.

作者信息

van Zwieten P A, Timmermans P B

出版信息

Eur J Clin Pharmacol. 1985;28 Suppl:13-9. doi: 10.1007/BF00543704.

Abstract

The penetration of beta-adrenoceptor blockers into the cerebrospinal fluid and into brain tissue is related to the lipophilicity of these drugs, as reflected by the partition coefficients between octanol and aqueous buffers. However, experimental techniques in animal models show no obvious relationships between the degree of brain penetration and the acute central antihypertensive effect of certain beta-blockers. This discrepancy is demonstrated convincingly by comparative experiments with atenolol and metoprolol. Both drugs are beta 1-selective blockers, and atenolol is highly polar, whereas metoprolol is lipophilic. Both these beta-blockers penetrate the CNS but to differing degrees. The experiments performed with these compounds support other studies described in the literature and do not suggest that there is a central mechanism which underlies the antihypertensive activity of beta-blockers.

摘要

β-肾上腺素受体阻滞剂进入脑脊液和脑组织的程度与这些药物的亲脂性有关,这一点通过辛醇与水性缓冲液之间的分配系数得以体现。然而,动物模型中的实验技术表明,某些β受体阻滞剂的脑渗透程度与急性中枢性降压作用之间并无明显关联。阿替洛尔和美托洛尔的对比实验令人信服地证明了这种差异。这两种药物都是β1选择性阻滞剂,阿替洛尔极性很高,而美托洛尔具有亲脂性。这两种β受体阻滞剂都能穿透中枢神经系统,但程度不同。用这些化合物进行的实验支持了文献中描述的其他研究,并未表明存在一种作为β受体阻滞剂降压活性基础的中枢机制。

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