Kuchel O, Léveillé J
Clinical Research Institute of Montreal, Hôtel-Dieu of Montreal Hospital and University of Montreal, Quebec, Canada.
Clin Auton Res. 1998 Dec;8(6):341-6. doi: 10.1007/BF02309625.
Unexplained episodic hypertension, hypotension, or orthostatic intolerance, tachycardia, anxiety, and flushing in 21 patients were investigated for the possibility of hypovolemia by blood volume and individual plasma catecholamines (including autocrine paracrine-born dopamine), determinations baseline, in response to upright posture and catecholamines only during the episodic blood pressure swings. Blood volume was determined by Cr51 fixed to patients' hemoglobin, free norepinephrine, epinephrine, and dopamine with dopamine sulfate following sulfatase hydrolysis, radioenzymatically. The recumbent mean 27.4+/-3% (SE) blood volume decrease from predicted values accentuating to 33.5+/-4% upright was associated with normal baseline plasma free norepinephrine, epinephrine, dopamine, dopamine sulfate, plasma renin activity, and aldosterone with normal mean postural responses from all patients except a hyperresponsive compared to controls (p < 0.04), plasma renin activity increase from 0.657+/-0.1 to 4.47+/-1.8 ng/mL/hr. During the hypertensive, hypotensive, or tachycardic episodes the moderate increase of free norepinephrine and epinephrine (p < 0.04) (but not free dopamine) contrasted with an increase of dopamine sulfate from 2.5+/-0.9 to clearly pathological values of 16.8+/-8.3 ng/mL (p < 0.0003 on % increase of individual values). We conclude that the normal (but to the degree of hypovolemia inappropriately low orthostatism- and episodes-associated sympathetic arousal) is outpaced by considerable episodic dopamine sulfate surges, reflecting extraneuronal dopamine discharge. Whether this increase contributes to the increased natriuresis directly or by inhibiting aldosterone response to renin-angiotensin, perpetuating hypovolemia, remains to be established.
对21例出现不明原因的发作性高血压、低血压或体位性不耐受、心动过速、焦虑和潮红的患者,通过血容量以及个体血浆儿茶酚胺(包括自分泌旁分泌产生的多巴胺)测定,在基线状态、对直立姿势的反应以及仅在发作性血压波动期间的儿茶酚胺水平来研究是否存在血容量不足的可能性。血容量通过固定在患者血红蛋白上的铬51、游离去甲肾上腺素、肾上腺素以及经硫酸酯酶水解后用硫酸多巴胺进行放射酶法测定的多巴胺来确定。卧位时血容量较预测值平均降低27.4±3%(标准误),直立时加重至33.5±4%,这与正常的基线血浆游离去甲肾上腺素、肾上腺素、多巴胺、硫酸多巴胺、血浆肾素活性和醛固酮水平相关,除了与对照组相比反应过度的患者(p<0.04)外,所有患者的平均体位反应均正常,血浆肾素活性从0.657±0.1增加到4.47±1.8 ng/mL/小时。在高血压、低血压或心动过速发作期间,游离去甲肾上腺素和肾上腺素适度增加(p<0.04)(但游离多巴胺未增加),与之形成对比的是硫酸多巴胺从2.5±0.9增加到明显异常的值16.8±8.3 ng/mL(个体值增加百分比p<0.0003)。我们得出结论,正常的(但与血容量不足程度不相称的低体位性和发作相关的交感神经兴奋)被大量发作性硫酸多巴胺激增所超越,这反映了神经外多巴胺的释放。这种增加是直接导致钠尿增加还是通过抑制醛固酮对肾素 - 血管紧张素的反应从而使血容量不足持续存在,仍有待确定。