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钠在糖尿病患者高血压中的核心作用。

Central role of sodium in hypertension in diabetic subjects.

作者信息

Weidmann P, Ferrari P

机构信息

Medizinische Poliklinik, University of Berne, Switzerland.

出版信息

Diabetes Care. 1991 Mar;14(3):220-32. doi: 10.2337/diacare.14.3.220.

Abstract

The common association between diabetes mellitus and hypertension may be promoted by several mechanisms. Patients with insulin-dependent (type I) diabetes and prone to develop nephropathy often have a familial predisposition for essential hypertension, whereas normotensive healthy offspring of nondiabetic essential hypertensive parents tend to have a reduced insulin sensitivity and increased plasma insulin levels. Na+ retention occurs as a characteristic alteration in type I or non-insulin-dependent (type II) diabetes; exchangeable body Na+ (Naex) is increased by 10% on average. This abnormality develops in the uncomplicated stage of diabetes and differentiates diabetic from nondiabetic essential hypertensive subjects. Possible Na(+)- retaining mechanisms include increased glomerular filtration of glucose leading to enhanced proximal tubular Na(+)-glucose cotransport, hyperinsulinemia (which activates several tubular Na+ transporters), an extravascular shift of fluid with Na+, and, once it occurs, renal failure. The pathogenetic role of Na+ retention in diabetes-associated hypertension is supported by positive correlations between systolic or mean blood pressure and Naex and by normalization of blood pressure after removal of excess Na+ by diuretic treatment in hypertensive diabetic subjects. The latter may also have an enhanced sensitivity of blood pressure to Na+. Plasma levels of active renin, angiotensin II, aldosterone, and catecholamines are usually normal or low in metabolically stable type I or type II diabetes. However, an exaggerated vascular reactivity to norepinephrine and angiotensin II commonly occurs already at uncomplicated stages of type I or type II diabetes. This may be a manifestation of functional (i.e., intracellular electrolytes) and/or morphological (proliferation, narrowing, and stiffening) vasculopathy. Diabetes-associated Na+ retention, vasculopathy, and a presumably inherited predisposition for both diabetes and essential hypertension may represent important complementary factors favoring the frequent occurrence of hypertension in the diabetic population.

摘要

糖尿病与高血压之间的常见关联可能由多种机制促成。胰岛素依赖型(I型)糖尿病且易患肾病的患者往往有原发性高血压的家族易感性,而非糖尿病原发性高血压患者的血压正常的健康后代往往胰岛素敏感性降低且血浆胰岛素水平升高。钠潴留是I型或非胰岛素依赖型(II型)糖尿病的特征性改变;可交换体钠(Naex)平均增加10%。这种异常在糖尿病的非并发症阶段就会出现,可将糖尿病患者与非糖尿病原发性高血压患者区分开来。可能的钠潴留机制包括肾小球滤过葡萄糖增加导致近端肾小管钠-葡萄糖协同转运增强、高胰岛素血症(激活多种肾小管钠转运体)、伴有钠的液体血管外转移,以及一旦发生则为肾衰竭。收缩压或平均血压与Naex之间的正相关以及高血压糖尿病患者经利尿剂治疗去除多余钠后血压恢复正常,均支持钠潴留在糖尿病相关性高血压发病机制中的作用。后者对钠的血压敏感性可能也增强。在代谢稳定的I型或II型糖尿病中,活性肾素、血管紧张素II、醛固酮和儿茶酚胺的血浆水平通常正常或降低。然而,在I型或II型糖尿病的非并发症阶段就常出现对去甲肾上腺素和血管紧张素II的血管反应性过度增强。这可能是功能性(即细胞内电解质)和/或形态学(增殖、狭窄和硬化)血管病变的表现。糖尿病相关的钠潴留、血管病变以及糖尿病和原发性高血压可能的遗传易感性,可能是促使糖尿病患者中高血压频繁发生的重要互补因素。

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