Key result
Minoxidil triggers massive pulmonary congestion and pleural effusion in rats with ascending aortic constriction.
Why the study?
The ability of the heart to express characteristic geometric features of concentric and eccentric hypertrophy concurrently under hemodynamic overload was unclear.
Does minoxidil accelerate heart failure development in rats with ascending aortic constriction?
Does minoxidil accelerate heart failure development in rats with ascending aortic constriction?
Minoxidil accelerates the development of heart failure in a rat model of pressure overload (aortic constriction) by causing unfavorable changes in left ventricular geometry and function.
Minoxidil may accelerate HF in pressure-overload models; leaves open relevance to human hypertension or aortic stenosis.
To test the ability of the heart to express characteristic geometric features of concentric and eccentric hypertrophy concurrently, constriction of the ascending aorta was performed in 4-week-old rats. Simultaneously, these rats were treated with an arteriolar dilator minoxidil. An examination 6 weeks after induction of the hemodynamic overload revealed no signs of congestion in systemic or pulmonary circulation in rats with aortic constriction or minoxidil-treated sham-operated rats. The magnitude of hemodynamic overload caused by aortic constriction or minoxidil treatment could be considered as equivalent, because the same enlargement of left ventricular pressure-volume area was necessary to compensate for either pressure or volume overload. Myocardial contractility decreased in rats with aortic constriction, and the compensation was achieved wholly by the marked concentric hypertrophy. Volume overload in minoxidil-treated rats was compensated partially by the eccentric hypertrophy and partially by the increased myocardial contractility. In contrast, increased lung weight and pleural effusion were found in all minoxidil-treated rats with aortic constriction. Unfavorable changes in left ventricular mass and geometry, relatively high chamber stiffness, and depressed ventricular and myocardial function were responsible for the massive pulmonary congestion.
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Turčáni et al. (1998) studied Ascending aortic constriction. Minoxidil vs. Aortic constriction alone and minoxidil-treated sham-operated rats was evaluated on Development of heart failure (pulmonary congestion, increased lung weight, pleural effusion). Minoxidil treatment in rats with ascending aortic constriction resulted in massive pulmonary congestion, increased lung weight, and pleural effusion at 6 weeks.
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