Gambardella S, Frontoni S, Pellegrinotti M, Testa G, Spallone V, Menzinger G
Cattedra di Malattie del Ricambio, Università di Roma Tor Vergata, Italy.
J Cardiovasc Pharmacol. 1993;22 Suppl 6:S87-97.
Epidemiologic studies suggest a close association between hypertension, obesity, and diabetes. It has been demonstrated that essential hypertension, per se, is an insulin-resistant state. However, the pathogenesis of the association between insulin resistance and hypertension is poorly understood. Elevated plasma insulin levels may contribute to the development of hypertension through renal sodium reabsorption, the sympathetic nervous system, the transmembranous cation transport, the renin-angiotensin system, the cardiovascular reactivity, and the atrial natriuretic peptide. Diuretics, beta-blockers, calcium antagonists, angiotensin-converting enzyme (ACE) inhibitors, and alpha 1-antagonists are first-choice drugs in the management of hypertension. Diuretics, except indapamide, impair insulin sensitivity and glucose tolerance. The same negative effects, exerted by beta-blockers, are reduced employing those with selective activity. With few exceptions, calcium antagonists have no adverse influence on carbohydrate metabolism. ACE inhibitors and alpha 1-antagonists do not influence or even improve glucose metabolism.
流行病学研究表明,高血压、肥胖症和糖尿病之间存在密切关联。业已证实,原发性高血压本身就是一种胰岛素抵抗状态。然而,胰岛素抵抗与高血压之间关联的发病机制尚不清楚。血浆胰岛素水平升高可能通过肾钠重吸收、交感神经系统、跨膜阳离子转运、肾素 - 血管紧张素系统、心血管反应性以及心房利钠肽等因素导致高血压的发生。利尿剂、β受体阻滞剂、钙拮抗剂、血管紧张素转换酶(ACE)抑制剂和α1受体拮抗剂是治疗高血压的首选药物。除吲达帕胺外,利尿剂会损害胰岛素敏感性和糖耐量。β受体阻滞剂也有同样的负面影响,使用具有选择性活性的β受体阻滞剂可减轻这些负面影响。除少数例外情况,钙拮抗剂对碳水化合物代谢无不良影响。ACE抑制剂和α1受体拮抗剂不会影响甚至会改善葡萄糖代谢。