Why the study?
Does ramipril alter the structure and in vitro function of subcutaneous small arteries in patients with mild heart failure post-myocardial infarction?
Does ramipril alter the structure and in vitro function of subcutaneous small arteries in patients with mild heart failure post-myocardial infarction?
ACE inhibitor therapy with ramipril in mild heart failure post-MI is associated with enhanced in vitro vasoconstriction to norepinephrine and angiotensin II in subcutaneous small arteries, possibly reflecting receptor upregulation.
Answers are grounded in this paper and cite their sources.
May increase vascular reactivity with ramipril post-MI; challenges expected ACEI effects on small-artery function.
The structure and function of subcutaneous small arteries from patients with mild heart failure (n = 27) 6-43 mo after myocardial infarction were compared with vessels from healthy control subjects (n = 10). Patients were randomized to treatment with placebo or the angiotensin-converting enzyme inhibitor ramipril starting 3-10 days after myocardial infarction. Dissected arterial vessels were mounted on a wire myograph for measurement of morphology and isometric tension. Morphology was not different in arteries from the three groups. Responses to norepinephrine, angiotensin II, and electrical field stimulation were similar in arteries from placebo-treated patients with mild heart failure and control subjects. Similarly, endothelium-dependent and -independent relaxation was normal in arteries from patients with mild heart failure. Ramipril therapy was associated with functional alterations: vasoconstrictor responses to norepinephrine and angiotensin II were significantly enhanced compared with placebo (P < 0.001). These data suggest that vascular structure and function are not different in vitro in subcutaneous arteries from placebo-treated patients with mild heart failure. Angiotensin-converting enzyme inhibitor therapy is associated with enhanced vasoconstriction to norepinephrine and angiotensin II, which may reflect upregulation of receptor-mediated events.
No takes yet. Share an insight, caveat, or question.
Stephens et al. (1998) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: