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α2 - 肾上腺素能拮抗剂育亨宾对直立耐受的影响。

Effect of the alpha 2-adrenergic antagonist yohimbine on orthostatic tolerance.

作者信息

Farrow S, Mers A, Banta G, Steigerwalt S, Lockette W

机构信息

Department of Medicine, Wayne State University School of Medicine, Detroit, MI 48201.

出版信息

Hypertension. 1990 Jun;15(6 Pt 2):877-80. doi: 10.1161/01.hyp.15.6.877.

DOI:10.1161/01.hyp.15.6.877
PMID:1972139
Abstract

We studied the effect of yohimbine, a drug that inhibits presynaptic alpha 2-adrenergic receptors and increases the neuronal release of norepinephrine from the central and sympathetic nervous systems, on tolerance to cardiovascular stress in 10 untrained, healthy subjects. Using radioligand binding of tritiated yohimbine to platelets, these subjects were found to have a normal complement of alpha 2-adrenergic receptors (174 +/- 18 [+/- SEM] receptors/platelet) with normal Kd (1.93 +/- 0.17 nmol/l). Lower body negative pressure was used to test responses to cardiovascular stress in the subjects after they received either placebo or 20 mg yohimbine. Graded lower body negative pressure from 0 to -40 mm Hg significantly decreased systolic blood pressure from 116 +/- 3.7 to 106 +/- 5.8 mm Hg, increased heart rate from 54 +/- 3 to 68 +/- 7 beats/min, decreased forearm blood flow from 1.8 +/- 0.21 to 1.36 +/- 0.25 ml/100 ml/min, and increased forearm vascular resistance from 55.76 +/- 12.1 to 77.26 +/- 15.8 mm Hg/ml/min. Yohimbine increased the blood pressure at rest and during lower body negative pressure, but these changes were not significantly different from values recorded from the individuals when they were given placebo. Compared with placebo, however, yohimbine significantly increased forearm blood flow at rest (1.80 +/- 0.21 vs. 2.66 +/- 0.31 ml/100 ml/min, p less than 0.05) and during -40 mm Hg of lower body negative pressure (1.36 +/- 0.25 vs. 1.91 +/- 0.28 ml/100 ml/min, p less than 0.05). We also found that yohimbine significantly increased the plasma insulin concentration in these fasted subjects (9.4 +/- 2.4 vs. 14.5 +/- 1.4 ng/ml, p less than 0.05) without inducing hypoglycemia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了育亨宾(一种抑制突触前α2-肾上腺素能受体并增加中枢和交感神经系统中去甲肾上腺素神经元释放的药物)对10名未经训练的健康受试者心血管应激耐受性的影响。通过用氚标记的育亨宾与血小板进行放射性配体结合试验,发现这些受试者具有正常数量的α2-肾上腺素能受体(174±18[±标准误]个受体/血小板),解离常数(Kd)也正常(1.93±0.17 nmol/l)。在受试者接受安慰剂或20毫克育亨宾后,使用下体负压来测试他们对心血管应激的反应。从0至-40毫米汞柱分级施加下体负压,可使收缩压从116±3.7显著降至106±5.8毫米汞柱,心率从54±3次/分钟增至68±7次/分钟,前臂血流量从1.8±0.21降至1.36±0.25毫升/100毫升/分钟,前臂血管阻力从55.76±12.1增至77.26±15.8毫米汞柱/毫升/分钟。育亨宾使静息时和下体负压期间的血压升高,但这些变化与给予安慰剂时个体记录的值无显著差异。然而,与安慰剂相比,育亨宾显著增加了静息时的前臂血流量(1.80±0.21对2.66±0.31毫升/100毫升/分钟,p<0.05)以及下体负压为-40毫米汞柱时的前臂血流量(1.36±0.25对1.91±0.28毫升/100毫升/分钟,p<0.05)。我们还发现,育亨宾显著增加了这些禁食受试者的血浆胰岛素浓度(9.4±2.4对14.5±1.4纳克/毫升,p<0.05),且未诱发低血糖。(摘要截短于250字)

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