Giffin M, Arthur G, Choy P C, Man R Y
Department of Pharmacology and Therapeutics, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
Can J Physiol Pharmacol. 1988 Mar;66(3):185-9. doi: 10.1139/y88-032.
The ability of exogenous lysophosphatidylcholine (LPC) to produce electrophysiological abnormalities in cardiac tissues and cardiac arrhythmias in isolated hearts has been well documented. In this study, the arrhythmogenic nature of LPC in the rat, rabbit, and guinea pig hearts was studied. The rat heart was found to be the most susceptible to LPC-induced arrhythmias, while the guinea pig heart was the least susceptible. Perfusion with labelled LPC revealed that the severity of arrhythmias correlates well with the amount of labelled LPC found in the microsomal membrane. The biochemical basis for the differences in the accumulation of LPC in the microsomal membrane of different animal species was investigated. Our results strongly indicate that the LPC level in the microsomal membrane may be regulated by the activity of microsomal lysophospholipase.
外源性溶血磷脂酰胆碱(LPC)在心脏组织中产生电生理异常以及在离体心脏中诱发心律失常的能力已有充分记录。在本研究中,对大鼠、兔和豚鼠心脏中LPC的致心律失常特性进行了研究。发现大鼠心脏对LPC诱导的心律失常最敏感,而豚鼠心脏最不敏感。用标记的LPC灌注显示,心律失常的严重程度与微粒体膜中发现的标记LPC量密切相关。研究了不同动物物种微粒体膜中LPC积累差异的生化基础。我们的结果有力地表明,微粒体膜中的LPC水平可能受微粒体溶血磷脂酶活性的调节。