Thrombolytic agents are used to restore coronary arlery per(uslon and Ilmtt the sire of a myocardial Infarcllon. The systemlc etfects of there drugs, streptoklnase (SK), urokinaae (UK), and recomblnant tlssue piaaminogen acllvator (rtPA), have been studied extensively. Although their ettscts on rheo
Hemodynamic effects of the D- and L-isomers of sotalol on normal myocardium
โ Scribed by Hans Martin Hoffmeister; Martin Beyer; Ludger Seipel
- Publisher
- Springer US
- Year
- 1991
- Tongue
- English
- Weight
- 566 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0920-3206
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โฆ Synopsis
This study investigated the hemodynamic effects of the D-isomer of sotalol in open-chest rats and compared this to the action of the L-isomer and the racemic DL-sotalol. Hemodynamic and additional isovolumic maximum measurements were registered at the end and 5 minutes after an intravenous infusion period of 7 minutes. DL-(1 and 2 mg/kg) and L-sotalol (2 mg/kg) caused a significant reduction in the heart rate and in the indices of contractility during and after infusion. D-sotalol (2, 4, and 8 mg/kg), however, decreased the contractility only transiently after very high doses at high plasma concentrations. Thus, while the effects of the beta-blocking L-isomer were comparable to those of DL-sota-!ol, only a slight and transient hemodynamic action of comparable doses of D-sotalol was found. These findings may be of significance for the proposed use of the D-isomer as a class-II! antiarrhythmic agent.
๐ SIMILAR VOLUMES
The pharmacokinetics of d-sotalol has been studied in six healthy volunteers given single doses of 0.25, 0.50, 1, 2 mg.kg-1 i.v. and one 100 mg oral dose in comparison with the kinetics of 1 mg.kg-1 i.v. of dl-sotalol. There was no significant difference in the disposition of the d-enantiomer and th