Abstract
1. A new compound designated as LASSBio 294 (L-294), 3,4-methylenedioxybenzoyl-2-thienylhydrazone, was synthesized as an alternative therapeutic for cardiac dysfunction. 2. L-294 increased in a dose-dependent manner the spontaneous contractions of isolated hearts from Wistar rats with maximal effect (128.0 ± 0.7% of control) observed at 25 μM. 3. The positive inotropic effect of L-294 was also observed in electrically stimulated cardiac tissues from Wistar rats. The maximal increment of twitches, at 200 μM, was 163.1 ± 18.4% for atrial, 153.5 ± 28.5% for papillary and 201.5 ± 18.5% for ventricular muscles. 4. In saponin skinned ventricular cells: (a) L-294 present in the period of sarcoplasmic reticulum (SR) loading with Ca2+ shifted the dose and caffeine-induced contracture curve; (b) L-294 (100 μM) increased 40% the Ca2+ uptake into SR; (c) L-294 did not significantly alter the sensitivity of contractile proteins to Ca2+ in SR-disrupted skinned ventricular cells. 5. Retrograde perfusion of the isolated heart from Wistar rats with L-294 (100 μM) did not cause any significant change in rhythm, heart rate (control, 220 ± 14.7 b.p.m.; 246 ± 24.6 b.p.m. for L-294), PR interval (control, 66.0 ± 2.4 ms; 64.0 ± 2.3 ms for L-294) or QRS duration (control, 28.8 ± 3.4 ms; 32.0 ± 2.0 ms for L-294). 6. These results suggest a novel mechanism for a positive cardioinotropic effect through an interaction with the Ca2+ uptake/release process of the SR. The effect of L-294 could be explained by a pronounced increased accumulation of Ca2+ into the SR.
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Sudo, R. T., Zapata-Sudo, G., & Barreiro, E. J. (2001). The new compound, LASSBio 294, increases the contractility of intact and saponin-skinned cardiac muscle from wistar rats. British Journal of Pharmacology, 134(3), 603–613. https://doi.org/10.1038/sj.bjp.0704291
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