Why the study?
Does continuous enalapril treatment for 6 weeks alter renal vascular responsiveness to vasoactive agents in anaesthetized rabbits?
Does continuous enalapril treatment for 6 weeks alter renal vascular responsiveness to vasoactive agents in anaesthetized rabbits?
Chronic ACE inhibition with enalapril for 6 weeks enhances, rather than reduces, renal vascular responsiveness to acetylcholine and angiotensin II in a rabbit model.
Hypothesis-generating for enhanced renal vascular responsiveness with chronic ACE inhibition in rabbits; leaves open translation to human practice.
OBJECTIVE: To determine whether 6 weeks continuous treatment with an angiotensin converting enzyme (ACE) inhibitor reduced renal vascular responsiveness in vivo, since this treatment results in extensive phenotypic conversion of afferent arteriolar cells from contractile to endocrine-like, renin secretory cells. METHODS: Enalapril (10 microg/kg per h s.c.) was delivered continuously for 6 weeks. In anaesthetized rabbits (treated or sham), arterial blood pressure and renal blood flow were measured and renal responsiveness tested by constructing dose-response curves to bolus doses of phenylephrine, angiotensin II and acetylcholine delivered directly into the renal artery. RESULTS: ACE inhibition resulted in a significant shift to the left in the renal vascular conductance responses to acetylcholine (P < 0.005) and angiotensin II (P < 0.05), indicating enhanced, not reduced, responsiveness to these agents. There were no significant effects of chronic ACE inhibition on the conductance responses to phenylephrine. CONCLUSIONS: Contrary to our hypothesis, 6 weeks ACE inhibition did not reduce renal vascular responsiveness to three vasoactive agents, suggesting that the phenotypic changes observed in the afferent arterioles and to a lesser extent the interlobular arteries, were either insignificant or compensated for by other changes in renal circulatory control.
No takes yet. Share an insight, caveat, or question.
Denton et al. (2001) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: