Szilvassy Z, Ferdinandy P, Szilvassy J, Nagy I, Karcsu S, Lonovics J, Dux L, Koltai M
First Department of Medicine, Albert Szent-Györgyi University Medical School of Szeged, Hungary.
J Mol Cell Cardiol. 1995 Dec;27(12):2559-69. doi: 10.1006/jmcc.1995.0043.
A brief rapid pacing has been shown to protect rabbit heart against global myocardial ischaemia induced by subsequent longer pacing. We studied whether pacing-induced preconditioning was reproducible in experimental hypercholesterolaemia. In conscious rabbits with an implanted right ventricular electrode and left ventricular polyethylene catheters, pacing of 500 bpm over 20 min induced an intracavitary ST-segment elevation of 3.2 +/- 0.41 mV, shortened ventricular effective refractory period and increased left ventricular end-diastolic pressure from prepacing 105 +/- 3.9 ms and 4.0 +/- 0.93 mmHg to post-pacing 62 +/- 6.4 ms and 27.9 +/- 7.2 mmHg, respectively. A 10-min preconditioning pacing followed by a 5-min interval markedly attenuated these test pacing-induced ischaemic changes. Rabbits were fed a cholesterol-enriched diet over 4, 8 and 12 weeks, responded to a 5- or 10-min pacing with ischaemic changes of the same degree as did controls to a 10- or 20-min pacing, respectively. A 4-week diet elevated total serum cholesterol from 1.7 +/- 0.4 to 24.1 +/- 2.9 mmol/l without apparent atherosclerotic lesions in the thoracic aorta assessed by Oil-Red O staining and planimetry, but it abolished protection induced by a 5-min preconditioning pacing. A 12-week diet increased serum cholesterol and lesion surface area to 26.9 +/- 3.2 mmol/l and 89.6 +/- 6.4%, respectively, and continued to block preconditioning. When these animals were refed normal chow over additional 6 weeks, serum cholesterol level dropped to 2.6 +/- 0.80 mmol/l with no change in atherosclerotic lesions, the preconditioning effect, however, recovered. We conclude that hypercholesterolaemia blocks preconditioning irrespective of the development of atherosclerosis.
短暂快速起搏已被证明可保护兔心脏免受随后较长时间起搏诱导的全心肌缺血影响。我们研究了起搏诱导的预处理在实验性高胆固醇血症中是否可重现。在植入右心室电极和左心室聚乙烯导管的清醒兔中,以500次/分钟的频率起搏20分钟可诱导腔内ST段抬高3.2±0.41 mV,缩短心室有效不应期,并使左心室舒张末期压力从起搏前的105±3.9毫秒和4.0±0.93毫米汞柱分别增加到起搏后的62±6.4毫秒和27.9±7.2毫米汞柱。10分钟的预处理起搏后间隔5分钟可显著减轻这些测试起搏诱导的缺血性变化。给兔喂食富含胆固醇的饮食4周、8周和12周,它们对5分钟或10分钟起搏的反应分别与对照组对10分钟或20分钟起搏的缺血性变化程度相同。4周的饮食使总血清胆固醇从1.7±0.4毫摩尔/升升高到24.1±2.9毫摩尔/升,经油红O染色和平面测量评估,胸主动脉无明显动脉粥样硬化病变,但它消除了5分钟预处理起搏诱导的保护作用。12周的饮食使血清胆固醇和病变表面积分别增加到26.9±3.2毫摩尔/升和89.6±6.4%,并继续阻断预处理。当这些动物再喂食正常食物6周后,血清胆固醇水平降至2.6±0.80毫摩尔/升,动脉粥样硬化病变无变化,然而,预处理效果恢复。我们得出结论,高胆固醇血症会阻断预处理,而与动脉粥样硬化的发展无关。