Aviv A, Aladjem M
Hypertension Research Center, University of Medicine & Dentistry of New Jersey, Newark 07103-2755.
Cardiovasc Drugs Ther. 1990 Mar;4 Suppl 2:335-42. doi: 10.1007/BF02603173.
Racial differences in the regulation of Na+, K+, and Ca2+ have been shown both at the systemic and cellular levels. These include a higher incidence of "salt sensitivity," lower urinary K+ excretion, lower plasma renin activity, and higher circulating levels of immunoreactive parathyroid hormone and 1.25 dihydroxyvitamin D in blacks than in whites. Blacks exhibit a higher erythrocyte Na+ concentration, coupled with a lower maximal initial reaction velocity of erythrocyte Na,K-ATPase. Blacks also appear to differ from whites in erythrocyte Na+, K+ cotransport and Na-Li countertransport. Moreover, they show a higher activity of the Na(+)-H+ antiport in skin fibroblasts and a greater response of cellular Ca2+ signaling to agonists in serum. Mechanisms linking some of these racial differences in ionic metabolism to the increased propensity of blacks to develop essential hypertension are proposed, and the epidemiology and characteristics of this disease in blacks are reviewed.
钠、钾和钙调节方面的种族差异在系统和细胞水平均已得到证实。这些差异包括,与白人相比,黑人中“盐敏感性”的发生率更高、尿钾排泄量更低、血浆肾素活性更低,以及免疫反应性甲状旁腺激素和1,25-二羟维生素D的循环水平更高。黑人的红细胞钠浓度较高,同时红细胞钠钾ATP酶的最大初始反应速度较低。黑人在红细胞钠、钾协同转运和钠-锂逆向转运方面似乎也与白人不同。此外,他们的皮肤成纤维细胞中钠氢反向转运体的活性较高,并且细胞钙信号对血清中激动剂的反应更大。本文提出了将这些离子代谢方面的种族差异中的一些差异与黑人患原发性高血压倾向增加联系起来的机制,并对黑人中这种疾病的流行病学和特征进行了综述。