Corr P B, Sobel B E
Adv Cardiol. 1980;27:346-60. doi: 10.1159/000384000.
Early malignant ventricular dysrhythmia induced by ischemia appear to depend on electrophysiological changes predisposing toward reentry. These changes are not readily explicable in terms of direct responses to hypoxia alone. Data from several laboratories make it increasingly clear that regional, heterogenous accumulations of noxious ions and metabolites play an important role. In addition to previously recognized factors including potassium, lactate, and hydrogen ion, both free and esterified fatty acid derivatives and metabolites of membrane phospholipids, particularly lysophosphoglycerides, have been implicated as potential mediators. Elucidation of the biochemical mechanisms responsible is of particular importance to development of prophylactic and therapeutic interventions with the needed specificity to be effective in reducing the incidence and severity of malignant ventricular dysrhythmia induced by ischemia and hence of sudden death.
缺血诱发的早期恶性室性心律失常似乎取决于易导致折返的电生理变化。这些变化仅用对缺氧的直接反应难以解释。多个实验室的数据越来越清楚地表明,有害离子和代谢产物的区域性、异质性蓄积起着重要作用。除了先前公认的因素,如钾、乳酸和氢离子外,游离和酯化的脂肪酸衍生物以及膜磷脂的代谢产物,特别是溶血磷酸甘油酯,也被认为是潜在的介质。阐明其生化机制对于开发具有所需特异性的预防和治疗干预措施尤为重要,这些措施能够有效降低缺血诱发的恶性室性心律失常的发生率和严重程度,从而降低猝死的发生率。