Mechanisms for blood pressure lowering and metabolic effects of thiazide and thiazide-like diuretics
- PMID: 20528637
- PMCID: PMC2904515
- DOI: 10.1586/erc.10.27
Mechanisms for blood pressure lowering and metabolic effects of thiazide and thiazide-like diuretics
Abstract
Thiazide and thiazide-like diuretics are among the most commonly used antihypertensives and have been available for over 50 years. However, the mechanism by which these drugs chronically lower blood pressure is poorly understood. Possible mechanisms include direct endothelial- or vascular smooth muscle-mediated vasodilation and indirect compensation to acute decreases in cardiac output. In addition, thiazides are associated with adverse metabolic effects, particularly hyperglycemia, and the mechanistic underpinnings of these effects are also poorly understood. Thiazide-induced hypokalemia, as well as other theories to explain these metabolic disturbances, including increased visceral adiposity, hyperuricemia, decreased glucose metabolism and pancreatic beta-cell hyperpolarization, may play a role. Understanding genetic variants with differential responses to thiazides could reveal new mechanistic candidates for future research to provide a more complete understanding of the blood pressure and metabolic response to thiazide diuretics.
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References
-
- Lloyd-Jones D, Adams R, Carnethon M, et al. Heart disease and stroke statistics – 2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation. 2009;119(3):480–486. - PubMed
-
- Chobanian AV, Bakris GL, Black HR, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension. 2003;42(6):1206–1252. - PubMed
-
- Ellison DH, Velazquez H, Wright FS. Thiazide-sensitive sodium chloride cotransport in early distal tubule. Am J Physiol. 1987;253(3 Pt 2):F546–F554. - PubMed
-
- Obermuller N, Bernstein P, Velazquez H, et al. Expression of the thiazide-sensitive Na–Cl cotransporter in rat and human kidney. Am J Physiol. 1995;269(6 Pt 2):F900–F910. - PubMed
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