4.7 Article

Effect of angiotensin II synthesis blockade on the hypertensive response to chronic reductions in uterine perfusion pressure in pregnant rats

Journal

HYPERTENSION
Volume 38, Issue 3, Pages 742-745

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/01.HYP.38.3.742

Keywords

hypertension, pregnancy; preeclampsia; renin-angiotensin system; enalapril; blood pressure

Funding

  1. NHLBI NIH HHS [HL51971, HL10137-01, HL38499] Funding Source: Medline

Ask authors/readers for more resources

The purpose of this study was to examine the role of the renin-angiotensin system in mediating the hypertension in response to chronic reductions in uterine perfusion pressure (RUPP) in conscious chronically instrumented pregnant rats. Mean arterial pressure was significantly higher in pregnant rats with chronic RUPP (125 +/-3.0 nim Hg, P <0.01, n=12) than in pregnant rats (100 +/-2.3 mm Hg, n=17). Plasma renin activity in pregnant rats with chronic RUPP was 17.1 +/-2.5 nmol angiotensin I . L-1 . h(-1) compared with 21.9 +/-3.5 nmol angiotensin I . L-1 . h(-1) in pregnant rats. Chronic oral administration of a converting-enzyme inhibitor (enalapril, 250 mg/L for 6 days) decreased mean arterial pressure to a similar extent in pregnant rats with chronic RUPP (109 +/-4.2 mm Hg, P <0.01, n=9) and in normal pregnant (81 +/-1.8 nun Hg, P <0.01, n=9) rats. Blockade of the renin-angiotensin system, however, had no significant effect on the blood pressure response to chronic RUPP as differences were similar in control (Delta 25 min Hg) and converting enzyme inhibitor-treated (Delta 27 mm Hg) groups. These findings suggest that the renin-angiotensin system does not play a major role in mediating the hypertension produced by chronic RUPP in pregnant rats.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available