Key result
BM 14.478 increased left ventricular dp/dt in rats, cats, and dogs, demonstrating an inotropic potency 5- to 18-fold higher than milrinone with no tolerance after 10 days of repeated administration.
Why the study?
Does BM 14.478 improve hemodynamic parameters in animal models?
Does BM 14.478 improve hemodynamic parameters in animal models?
BM 14.478 is a novel positive inotropic and vasodilating agent that demonstrates greater potency and a longer duration of action than milrinone in preclinical models.
BM 14.478 (7,7-dimethyl-2-(4-pyridyl)-6,7-dihydro-3H,5H pyrrolo [2,3-f]benz-imidazol-6-one) was investigated in anesthetized rats and cats and conscious dogs. Left ventricular dp/dt was increased after intravenous injection of 0.01-0.1 mg/kg in rats (7,200 +/- 300 to 10,700 +/- 500 mm Hg/s), 0.001-0.3 mg/kg in cats (2,800 +/- 200 to 4,500 +/- 100 mm Hg/s) and 0.01 +/- 3.0 mg/kg in dogs (2,400 +/- 100 to 4,400 +/- 500 mm Hg/s). The inotropic potency was about 5- to 18-fold higher than that of milrinone. Effects persisted for more than 6.5 h in dogs after administration of 1 mg/kg p.o., which was definitely longer than that of milrinone. Hypotension and a moderate tachycardia were observed in the same dose range. In conscious dogs the compound increased cardiac output by 39 +/- 10%, and stroke volume by 17 +/- 7% and lowered total peripheral resistance by 45 +/- 5% and right atrial pressure by 3.0 +/- 0.3 mm Hg. BM 14.478 induced no tolerance after repeated administration in dogs when administered in a dose of 1 mg/kg p.o. b.i.d. for 10 days.
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Müller‐Beckmann et al. (1988) studied this question. BM 14.478 vs. Milrinone was evaluated on Left ventricular dp/dt. BM 14.478 increased left ventricular dp/dt in rats, cats, and dogs, demonstrating an inotropic potency 5- to 18-fold higher than milrinone with no tolerance after 10 days of repeated administration.
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