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非调节性高血压患者去甲肾上腺素和醛固酮对直立姿势的异常反应。

Abnormal norepinephrine and aldosterone responses to upright posture in nonmodulating hypertension.

作者信息

Conlin P R, Braley L M, Menachery A I, Hollenberg N K, Williams G H

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

出版信息

J Clin Endocrinol Metab. 1992 Oct;75(4):1017-21. doi: 10.1210/jcem.75.4.1400865.

Abstract

The subgroup of patients with nonmodulating hypertension demonstrates a number of abnormalities of the renin-angiotensin-aldosterone axis. We previously identified abnormalities in plasma and urinary dopamine in nonmodulators and posited that this may be in part due to a generalized defect in sympathetic nervous system activity. In the present study we assessed the state of activation of the renin-angiotensin system and the sympathetic nervous system in normal subjects and patients with modulating, nonmodulating, and low renin essential hypertension during sodium depletion and change from supine to upright posture. Levels of plasma norepinephrine were higher in non-modulators during the posture study (P < 0.05). PRA rose with upright posture in all groups, but low renin subjects had a blunted response. Nonmodulators and low renin subjects had lower aldosterone levels both supine (P< 0.05) and upright (P< 0.01). However, the aldosterone/PRA increment ratio was increased in low renin subjects (P< 0.01), whereas it was decreased in nonmodulators. Twenty-four-hour urine collections for catecholamine determinations were obtained in a subgroup of the subjects, with nonmodulators showing higher levels of norepinephrine excretion which approached significance (P = 0.08). In vitro experiments using rat and human adrenal glomerulosa cells showed that norepinephrine does not affect aldosterone secretion per se. These observations extend the series of abnormalities observed in nonmodulating hypertension. However, it is likely that the alterations in norepinephrine levels during sodium depetion and upright posture are a secondary event and not linked to the altered aldosterone production in these patients.

摘要

非调节性高血压患者亚组表现出肾素-血管紧张素-醛固酮轴的一些异常。我们之前在非调节性高血压患者中发现血浆和尿多巴胺异常,并推测这可能部分归因于交感神经系统活动的普遍缺陷。在本研究中,我们评估了正常受试者以及调节性、非调节性和低肾素原发性高血压患者在钠缺失期间以及从仰卧位变为直立位时肾素-血管紧张素系统和交感神经系统的激活状态。在体位研究中,非调节性高血压患者的血浆去甲肾上腺素水平较高(P < 0.05)。所有组的血浆肾素活性(PRA)均随直立位升高,但低肾素患者的反应减弱。非调节性高血压患者和低肾素患者仰卧位(P< 0.05)和直立位(P< 0.01)时醛固酮水平均较低。然而,低肾素患者的醛固酮/PRA增加值比率升高(P< 0.01),而非调节性高血压患者的该比率降低。在部分受试者亚组中进行了24小时尿儿茶酚胺测定,非调节性高血压患者的去甲肾上腺素排泄水平较高,接近显著水平(P = 0.08)。使用大鼠和人肾上腺球状带细胞进行的体外实验表明,去甲肾上腺素本身并不影响醛固酮分泌。这些观察结果扩展了在非调节性高血压中观察到的一系列异常情况。然而,钠缺失和直立位期间去甲肾上腺素水平的变化可能是继发事件,与这些患者醛固酮生成改变无关。

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