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卡维地洛立体异构体的药理学特性。

Pharmacological characteristics of the stereoisomers of carvedilol.

作者信息

Bartsch W, Sponer G, Strein K, Müller-Beckmann B, Kling L, Böhm E, Martin U, Borbe H O

机构信息

Department of Cardiovascular Research, Boehringer Mannheim GmbH, Federal Republic of Germany.

出版信息

Eur J Clin Pharmacol. 1990;38 Suppl 2:S104-7. doi: 10.1007/BF01409475.

Abstract

The racemic compound carvedilol possesses two complementary pharmacological effects, vasodilation and beta-blockade. The R- and S-enantiomers of carvedilol and the racemate were investigated with respect to the beta-blocking, vasodilating, and hypotensive actions. In agreement with results obtained with other beta-blockers, only the S-enantiomer of carvedilol exerts beta-blocking effects. In contrast, no substantial difference between the enantiomers could be seen with respect to alpha-blockade. The greater hypotensive activity of S-carvedilol may be attributed to beta-blockade, which inhibits counter-regulatory mechanisms provoked by vasodilation. From these results it is concluded that there is a rationale for using carvedilol as the racemate. Using the S-enantiomer would lead to relatively strong beta-blockade with only a weak vasodilating effect. The R-enantiomer alone would act only as a hypotensive agent without beta-blockade.

摘要

消旋化合物卡维地洛具有两种互补的药理作用,即血管舒张和β受体阻滞。对卡维地洛的R-和S-对映体以及外消旋体的β受体阻滞、血管舒张和降压作用进行了研究。与其他β受体阻滞剂的结果一致,只有卡维地洛的S-对映体具有β受体阻滞作用。相比之下,在α受体阻滞方面,对映体之间没有明显差异。S-卡维地洛较强的降压活性可能归因于β受体阻滞,它抑制了血管舒张引发的反调节机制。从这些结果可以得出结论,使用卡维地洛外消旋体是有道理的。使用S-对映体将导致相对较强的β受体阻滞,而血管舒张作用较弱。单独使用R-对映体仅作为一种无β受体阻滞作用的降压药。

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