Olesin A I, Pavlova R N, Lobanov N A
Ter Arkh. 1991;63(4):82-6.
Overall 93 patients suffering from coronary heart disease /CHD/ (without acute myocardial infarction) complicated by cardiac rhythm impairment were followed up. Investigation of lipid peroxidation (LPO) and of the antioxidant system (AOS) in those patients revealed LPO activation and a decrease of the AOS activity both at the moment of arrhythmia and after its arrest, with the highest LPO activation being seen in the hyper- and hypokinetic hemodynamic variants. The experimental studies have demonstrated a reverse relationship between the rise of LPO products in the blood, LPO activation in myocytes and the onset of arrhythmia because of an increase in the density of Na(+)-Ca++ channels of the membrane, accumulation of those ions by the cell, and an increase of the transmembranous potential at rest. Therefore, to prevent and treat cardiac rhythm impairment in CHD patients, it is necessary to administer the blockers of Na(+)-Ca++ channels (etmozin, ethacizine, verapamil and so forth) and antioxidants that raise the reserve capacity of the AOS, including laser therapy.
对93例患有冠心病(无急性心肌梗死)并伴有心律失常的患者进行了随访。对这些患者的脂质过氧化(LPO)和抗氧化系统(AOS)进行调查发现,在心律失常发作时及其终止后,LPO均被激活,AOS活性降低,其中以高动力和低动力血流动力学变体中的LPO激活最为明显。实验研究表明,血液中LPO产物的增加、心肌细胞中LPO的激活与心律失常的发生之间存在反向关系,这是由于膜上Na(+)-Ca++通道密度增加、细胞对这些离子的蓄积以及静息跨膜电位升高所致。因此,为预防和治疗冠心病患者的心律失常,有必要给予Na(+)-Ca++通道阻滞剂(乙胺碘呋酮、乙噻嗪、维拉帕米等)以及提高AOS储备能力的抗氧化剂,包括激光治疗。