Salt, aldosterone, and insulin resistance: impact on the cardiovascular system

被引:101
作者
Lastra, Guido [1 ]
Dhuper, Sonal [2 ]
Johnson, Megan S. [1 ]
Sowers, James R. [1 ]
机构
[1] Univ Missouri, Sch Med, HSC Diabet Ctr D109, Dept Internal Med,Div Endocrinol & Diabet, Columbia, MO 65212 USA
[2] Univ Missouri, Sch Med, HSC Diabet Ctr D109, Dept Internal Med,Div Gen Internal Med, Columbia, MO 65212 USA
关键词
LEFT-VENTRICULAR DYSFUNCTION; RENIN-ANGIOTENSIN SYSTEM; BLOOD-PRESSURE; MINERALOCORTICOID RECEPTOR; PLASMA-ALDOSTERONE; DIABETES-MELLITUS; OXIDATIVE STRESS; DIETARY-SODIUM; HYPERTENSION; SENSITIVITY;
D O I
10.1038/nrcardio.2010.123
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypertension and type 2 diabetes mellitus (T2DM) are powerful risk factors for cardiovascular disease (CVD) and chronic kidney disease (CKD), both of which are leading causes of morbidity and mortality worldwide. Research into the pathophysiology of CVD and CKD risk factors has identified salt sensitivity and insulin resistance as key elements underlying the relationship between hypertension and T2DM. Excess dietary salt and caloric intake, as commonly found in westernized diets, is linked not only to increased blood pressure, but also to defective insulin sensitivity and impaired glucose homeostasis. In this setting, activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS), as well as increased signaling through the mineralocorticoid receptor (MR), result in increased production of reactive oxygen species and oxidative stress, which in turn contribute to insulin resistance and impaired vascular function. In addition, insulin resistance is not limited to classic insulin-sensitive tissues such as skeletal muscle, but it also affects the cardiovascular system, where it participates in the development of CVD and CKD. Current clinical knowledge points towards an impact of salt restriction, RAAS blockade, and MR antagonism on cardiovascular and renal protection, but also on improved insulin sensitivity and glucose homeostasis.
引用
收藏
页码:577 / 584
页数:8
相关论文
共 75 条
[1]   IMMUNOCHEMICAL DETECTION OF THE MINERALOCORTICOID RECEPTOR IN RAT-BRAIN [J].
AGARWAL, MK ;
MIRSHAHI, F ;
MIRSHAHI, M ;
ROSTENE, W .
NEUROENDOCRINOLOGY, 1993, 58 (05) :575-580
[2]   Fasting glucose levels and incident diabetes mellitus in older nondiabetic adults randomized to receive 3 different classes of antihypertensive treatment - A report from the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) [J].
Barzilay, Joshua I. ;
Davis, Barry R. ;
Cutler, Jeffrey A. ;
Pressel, Sara L. ;
Whelton, Paul K. ;
Basile, Jan ;
Margolis, Karen L. ;
Ong, Stephen T. ;
Sadler, Laurie S. ;
Summerson, John .
ARCHIVES OF INTERNAL MEDICINE, 2006, 166 (20) :2191-2201
[3]   Plasma aldosterone is independently associated with the metabolic syndrome [J].
Bochud, Murielle ;
Nussberger, Jurg ;
Bovet, Pascal ;
Maillard, Marc R. ;
Elston, Robert C. ;
Paccaud, Fred ;
Shamlaye, Conrad ;
Burnier, Michel .
HYPERTENSION, 2006, 48 (02) :239-245
[4]  
Bosch J, 2006, NEW ENGL J MED, V355, P1551
[5]  
BRILLA CG, 1992, J LAB CLIN MED, V120, P893
[6]   Aldosterone and vascular inflammation [J].
Brown, Nancy J. .
HYPERTENSION, 2008, 51 (02) :161-167
[7]   Pivotal role of the mineralocorticoid receptor in corticosteroid-induced adipogenesis [J].
Caprio, Massimiliano ;
Feve, Bruno ;
Claes, Aurelie ;
Viengchareun, Say ;
Lombes, Marc ;
Zennaro, Maria-Christina .
FASEB JOURNAL, 2007, 21 (09) :2185-2194
[8]   The new biology of aldosterone [J].
Connell, JMC ;
Davies, E .
JOURNAL OF ENDOCRINOLOGY, 2005, 186 (01) :1-20
[9]   Renin-angiotensin-aldosterone system and oxidative stress in cardiovascular insulin resistance [J].
Cooper, Shawna A. ;
Whaley-Connell, Adam ;
Habibi, Javad ;
Wei, Yongzhong ;
Lastra, Guido ;
Manrique, Camila ;
Stas, Sameer ;
Sowers, James R. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 293 (04) :H2009-H2023
[10]   Hyperinsulinemia as an independent risk factor for ischemic heart disease [J].
Despres, JP ;
Lamarche, B ;
Mauriege, P ;
Cantin, B ;
Dagenais, GR ;
Moorjani, S ;
Lupien, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (15) :952-957