4.5 Article

Increased sensitivity of the obese Zucker rat to deoxycorticosterone-salt-induced hypertension

Journal

JOURNAL OF HYPERTENSION
Volume 20, Issue 11, Pages 2247-2255

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00004872-200211000-00025

Keywords

deoxycorticosterone acetate; hypertension; kidney; obese Zucker rat; obesity-associated hypertension

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Objective The objective of this study was to test the hypothesis that obesity increases the sensitivity of rats to experimentally induced hypertension. Design and methods To induce hypertension, unilaterally nephrectornized lean and obese Zucker rats were injected with 25 mg/kg of deoxycorticosterone acetate (DOCA) twice weekly for 5 weeks and given water containing 1% NaCl to drink. Unilaterally nephrectornized control rats were injected with vehicle and drank tap water. Systolic blood pressure (SBP) was measured by the tail cuff method. Renal histology and urinary albumin excretion were used to assess the effects of the experimental treatment on the kidney. Results Obese rats exhibited a significant rise in SBP at 4 days after the start of DOCA-salt treatment. In contrast, SBP of DOCA-treated lean rats was not significantly elevated from pretreatment measurements until day 22. Moreover, SBP was significantly higher during the plateau phase of blood pressure development in obese DOCA-salt treated rats (196 mmHg) than in correspondingly treated lean rats (150 mmHg). Both obesity and DOCA-salt treatment promoted glomerulosclerosis and mild tubulointerstitial damage in the kidney with DOCA-salt treatment exacerbating the effect of obesity. Urinary albumin excretion was significantly greater in obese control rats compared with lean controls and in DOCA-treated obese rats relative to vehicle-treated obese rats. Conclusion Results of this study indicate that obese Zucker rats are more sensitive to mineralocorticoid-induced hypertension than lean rats. This study provides experimental evidence supporting the epidemiological findings that obesity is a risk factor for the development of hypertension. (C) 2002 Lippincott Williams Wilkins.

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