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原发性高血压患者血浆去甲肾上腺素和二羟苯乙二醇水平

Plasma norepinephrine and dihydroxyphenylglycol in essential hypertension.

作者信息

Ludwig J, Gerlich M, Halbrügge T, Graefe K H

机构信息

Medizinische Poliklinik, University of Würzburg, FRG.

出版信息

Hypertension. 1991 Apr;17(4):546-52. doi: 10.1161/01.hyp.17.4.546.

DOI:10.1161/01.hyp.17.4.546
PMID:2013481
Abstract

The aim of the present study was to examine whether essential hypertension is associated with altered plasma concentrations of dihydroxyphenylglycol, the principal presynaptic metabolite of norepinephrine. Forearm venous plasma dihydroxyphenylglycol and norepinephrine were determined at rest and during graded orthostasis in 47 normotensive control subjects and 58 outpatients with essential hypertension. There was no group difference in age. At supine rest as well as during sitting and standing, hypertensive subjects had plasma norepinephrine concentrations similar to those in normotensive control subjects, but plasma dihydroxyphenylglycol concentrations were higher than those in normotensive control subjects. Both groups showed a linear relation between plasma dihydroxyphenylglycol (ordinate) and plasma norepinephrine (abscissa). The resulting regression line was steeper (p less than 0.02) and its ordinate intercept higher (p less than 0.01) in hypertensive than in control subjects. Eleven normotensive and 14 hypertensive subjects were also tested 3 hours after desipramine (1.5 mg/kg orally) was administered to inhibit neuronal norepinephrine reuptake. The drug did not alter plasma norepinephrine, but did reduce plasma dihydroxyphenylglycol and did abolish plasma dihydroxyphenylglycol responses to upright posture in both groups of subjects. The mean plasma dihydroxyphenylglycol concentration observed in the presence of desipramine again was higher in the hypertensive than in the control group (p less than 0.01) and closely agreed, in both groups, with the dihydroxyphenylglycol concentration given by the ordinate intercept of the dihydroxyphenylglycol versus norepinephrine regression line in the absence of desipramine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是检验原发性高血压是否与去甲肾上腺素的主要突触前代谢产物二羟基苯乙二醇的血浆浓度改变有关。在47名血压正常的对照受试者和58名原发性高血压门诊患者中,于静息状态和分级直立位时测定了前臂静脉血浆中二羟基苯乙二醇和去甲肾上腺素的水平。两组在年龄上无差异。在仰卧位静息时以及坐位和站立时,高血压患者的血浆去甲肾上腺素浓度与血压正常的对照受试者相似,但血浆二羟基苯乙二醇浓度高于血压正常的对照受试者。两组均显示血浆二羟基苯乙二醇(纵坐标)与血浆去甲肾上腺素(横坐标)之间呈线性关系。高血压患者的回归直线比对照组更陡峭(p<0.02),其纵坐标截距更高(p<0.01)。还对11名血压正常者和14名高血压患者在口服地昔帕明(1.5mg/kg)以抑制神经元去甲肾上腺素再摄取3小时后进行了测试。该药物未改变血浆去甲肾上腺素水平,但降低了血浆二羟基苯乙二醇水平,并消除了两组受试者血浆二羟基苯乙二醇对直立姿势的反应。在使用地昔帕明的情况下,观察到的高血压组血浆二羟基苯乙二醇平均浓度再次高于对照组(p<0.01),并且在两组中,该浓度与在未使用地昔帕明时二羟基苯乙二醇与去甲肾上腺素回归直线的纵坐标截距所对应的二羟基苯乙二醇浓度密切相符。(摘要截短至250字)

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引用本文的文献

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Naunyn Schmiedebergs Arch Pharmacol. 1993 Feb;347(2):162-70. doi: 10.1007/BF00169262.
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Plasma normetanephrine for examination of extraneuronal uptake and metabolism of noradrenaline in rats.血浆去甲变肾上腺素用于大鼠去甲肾上腺素的非神经元摄取和代谢研究。
Naunyn Schmiedebergs Arch Pharmacol. 1994 Mar;349(3):259-69. doi: 10.1007/BF00169292.