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奈必洛尔立体异构体对肾上腺素在血压、心率以及去甲肾上腺素和多巴胺水平方面作用的影响。

Effects of nebivolol stereoisomers on the action of adrenaline on blood pressure, heart rate and blood levels of noradrenaline and DOPEG.

作者信息

Borges N, Martel F, Branco D, Osswald W

机构信息

Department of Pharmacology and Therapeutics, Faculty of Medicine, Porto, Portugal.

出版信息

J Auton Pharmacol. 1992 Dec;12(6):429-35. doi: 10.1111/j.1474-8673.1992.tb00391.x.

Abstract
  1. Nebivolol (a new beta 1-adrenoceptor blocking drug) has particular effects on the cardiovascular system, i.e. it induces hypotension without affecting cardiac function or increasing peripheral vascular resistances. In this study, we aimed to evaluate the effects of nebivolol and its stereoisomers on the actions of adrenaline (AD) at the cardiovascular level as well as at the prejunctional level (as ascertained by modification of noradrenaline (NA) and dihydroxyphenylglycol (DOPEG) plasma levels in the anaesthetized dog. 2. AD infusion (0.1 micrograms kg-1 min-1) did not induce statistically significant changes in mean blood pressure and heart rate; it caused a pronounced and sustained rise of AD levels, no significant alterations in NA levels and a marked, progressive and sustained increase in DOPEG levels. 3. Mean blood pressure was not affected by any of the nebivolol isomers. d- and dl-nebivolol in the two doses used (0.3 and 0.03 mg kg-1 in 15 min) caused a significant and dose-dependent decrease in heart rate. Plasma levels of AD and NA were not changed by any of the nebivolol isomers tested. However, all of them significantly reduced the increase in plasma levels of DOPEG induced by adrenaline infusion. 4. We conclude (1) that AD infusion in the dog facilitates NA release and that DOPEG is a good index of this effect; and (2) nebivolol appears to act at the prejunctional level, reducing the increase in NA release induced by adrenaline, as shown by the effect on DOPEG plasma levels.
摘要
  1. 奈必洛尔(一种新型β1 - 肾上腺素能受体阻断药物)对心血管系统有特殊作用,即它能引起低血压,而不影响心脏功能或增加外周血管阻力。在本研究中,我们旨在评估奈必洛尔及其立体异构体在心血管水平以及突触前水平对肾上腺素(AD)作用的影响(通过麻醉犬血浆中去甲肾上腺素(NA)和二羟基苯乙二醇(DOPEG)水平的变化来确定)。2. 输注AD(0.1微克·千克-1·分钟-1)未引起平均血压和心率的统计学显著变化;它导致AD水平显著且持续升高,NA水平无显著改变,DOPEG水平显著、逐渐且持续升高。3. 平均血压不受任何奈必洛尔异构体的影响。所用两种剂量(15分钟内0.3和0.03毫克·千克-1)的d - 奈必洛尔和dl - 奈必洛尔引起心率显著且剂量依赖性降低。所测试的任何奈必洛尔异构体均未改变AD和NA的血浆水平。然而,它们均显著降低了肾上腺素输注诱导的DOPEG血浆水平升高。4. 我们得出结论:(1)犬输注AD促进NA释放,且DOPEG是此效应的良好指标;(2)如对DOPEG血浆水平的影响所示,奈必洛尔似乎作用于突触前水平,减少肾上腺素诱导的NA释放增加。

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