Article date: February 2001
By: J van Klarenbosch, G J M Stienen, W de Ruijter, G J Scheffer, J J de Lange in Volume 132, Issue 3, pages 742-748
The effects of propofol on myocardial contractility were studied in rat, in which the contractile activation mainly depends on calcium derived from the sarcoplasmic reticulum (SR), and guinea‐pig, in which transsarcolemmal influx of calcium plays a major role.
Intact and chemically skinned trabeculae from the right ventricle were studied. Intact trabeculae were electrically stimulated and force development during steady state and post rest contractions was measured. In saponin skinned trabeculae Ca2+ uptake and release by the SR was studied. In Triton skinned trabeculae the influence of propofol on calcium sensitivity of the myofilaments was studied.
In intact rat trabeculae propofol in concentrations of 28, 112 and 280 μM did not change peak force development nor the pattern of post rest contraction. In guinea‐pig trabeculae propofol significantly reduced peak force to respectively 64, 40 and 23% of control values and the post rest contractions were potentiated. In skinned trabeculae propofol did not affect Ca2+ handling by the SR, nor did it change force production and Ca2+ sensitivity of the myofilaments.
This study shows that, in contrast to rat, in guinea‐pig propofol directly depresses myocardial contractility, probably by decreasing transsarcolemmal Ca2+ influx. There is no significant influence of propofol on Ca2+ handling by the SR, nor on the contractile proteins.
The effects of propofol on myocardial contractility were studied in rat, in which the contractile activation mainly depends on calcium derived from the sarcoplasmic reticulum (SR), and guinea‐pig, in which transsarcolemmal influx of calcium plays a major role.
Intact and chemically skinned trabeculae from the right ventricle were studied. Intact trabeculae were electrically stimulated and force development during steady state and post rest contractions was measured. In saponin skinned trabeculae Ca2+ uptake and release by the SR was studied. In Triton skinned trabeculae the influence of propofol on calcium sensitivity of the myofilaments was studied.
In intact rat trabeculae propofol in concentrations of 28, 112 and 280 μM did not change peak force development nor the pattern of post rest contraction. In guinea‐pig trabeculae propofol significantly reduced peak force to respectively 64, 40 and 23% of control values and the post rest contractions were potentiated. In skinned trabeculae propofol did not affect Ca2+ handling by the SR, nor did it change force production and Ca2+ sensitivity of the myofilaments.
This study shows that, in contrast to rat, in guinea‐pig propofol directly depresses myocardial contractility, probably by decreasing transsarcolemmal Ca2+ influx. There is no significant influence of propofol on Ca2+ handling by the SR, nor on the contractile proteins.
British Journal of Pharmacology (2001) 132, 742–748; doi:10.1038/sj.bjp.0703849
DOI: 10.1038/sj.bjp.0703849
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