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β-肾上腺素能受体阻滞剂对运动诱导的血浆儿茶酚胺浓度与心率反应关系的影响。

Effect of beta-adrenoceptor blockade on exercise-induced plasma catecholamine concentration-heart rate response relationship.

作者信息

Ohnishi A, Minegishi A, Ishizaki T

机构信息

Division of Clinical Pharmacology, National Medical Center, Tokyo, Japan.

出版信息

J Cardiovasc Pharmacol. 1987 Dec;10(6):667-74. doi: 10.1097/00005344-198712000-00010.

Abstract

We examined the chronotropic and sympathoadrenal responses to a strenuous exercise in eight normal subjects receiving placebo and carteolol, a nonselective beta-adrenoceptor blocker. Plasma catecholamines were measured with high-performance liquid chromatography with electrochemical detection (HPLC-ECD). Mean plasma norepinephrine (NE) and epinephrine (E) concentrations attained at 0.5 and 2 min after exercise were significantly (p less than 0.001-0.05) greater in the carteolol trial than in the placebo trial and approached concentrations fairly similar to preexercise baseline values by 15 min after cessation of exercise in the two trials. The postexercise plasma NE and E concentration-chronotropic response relationships were shifted to the right in the carteolol as compared with the placebo phase. The maximal postexercise NE concentrations measured during the placebo trial correlated significantly with beta-adrenoceptor blockade (p less than 0.05, r = 0.74), whereas the relationship between E concentrations and beta-adrenoceptor blockade did not reach significant level in this small group of study subjects. The results suggest that beta-adrenoceptor blockade increases plasma concentrations of both NE and E during an earlier postexercise period and may cause a greater reflex sympathetic activation as compared with the adrenal response. However, the mechanism(s) remains unclear. Whether the exercise-induced NE rather than E would participate more predominantly in the chronotropic response to beta-adrenoceptor blockade requires further studies.

摘要

我们研究了8名接受安慰剂和非选择性β肾上腺素受体阻滞剂卡替洛尔的正常受试者在剧烈运动时的变时性和交感肾上腺反应。采用高效液相色谱电化学检测法(HPLC - ECD)测定血浆儿茶酚胺。运动后0.5分钟和2分钟时,卡替洛尔试验中的平均血浆去甲肾上腺素(NE)和肾上腺素(E)浓度显著高于安慰剂试验(p<0.001 - 0.05),且在两项试验中运动停止后15分钟时接近与运动前基线值相当的浓度。与安慰剂阶段相比,卡替洛尔组运动后血浆NE和E浓度 - 变时性反应关系向右移动。安慰剂试验期间测得的运动后最大NE浓度与β肾上腺素受体阻滞显著相关(p<0.05,r = 0.74),而在这一小群研究对象中,E浓度与β肾上腺素受体阻滞之间的关系未达到显著水平。结果表明,与肾上腺反应相比,β肾上腺素受体阻滞在运动后早期会增加NE和E的血浆浓度,并可能导致更大的反射性交感神经激活。然而,其机制尚不清楚。运动诱导的NE而非E是否在β肾上腺素受体阻滞的变时性反应中起更主要作用,需要进一步研究。

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