首页> 外文期刊>American Journal of Physiology >Cholesterol diet-induced hyperlipidemia impairs the cardioprotective effect of postconditioning: role of peroxynitrite.
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Cholesterol diet-induced hyperlipidemia impairs the cardioprotective effect of postconditioning: role of peroxynitrite.

机译:胆固醇饮食诱导的高脂血症损害后后台的心脏保护作用:过氧硝酸盐的作用。

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摘要

The aim of the present study was to investigate if hyperlipidemia interferes with the infarct size-limiting effect of postconditioning and to study the involvement of peroxynitrite in this phenomenon. Rats were fed a 2% cholesterol-enriched or normal diet for 12 wk. Infarct size by triphenyltetrazolium chloride staining was measured in hearts isolated from both groups and subjected to 30 min coronary occlusion followed by 120 min reperfusion with or without the postconditioning protocol induced by six cycles of 10 s coronary occlusion and 10 s reperfusion at the onset of the reperfusion. Postconditioning significantly decreased infarct size in the normolipidemic but not in the hyperlipidemic group. Postconditioning increased cardiac 3-nitrotyrosine concentration (a marker for peroxynitrite formation) in the normal but not in the cholesterol-fed group when measured at the 5th min of reperfusion. Next, we tested if the postconditioning-induced acute increase in peroxynitrite is involved in the cardioprotection in normolipidemic animals in separate experiments. Postconditioning failed to decrease infarct size in the presence of the peroxynitrite decomposition catalyst 5,10,15,20-tetrakis-[4-sulfonatophenyl]-porphyrinato-iron [III] (20 mg/l) in normolipidemic animals. We conclude that an early increase in peroxynitrite after postconditioning plays a role in cardioprotection. Furthermore, hyperlipidemia blocks the cardioprotective effect of postconditioning at least in part via deterioration of the postconditioning-induced early increase in peroxynitrite formation.
机译:本研究的目的是调查高脂血症是否干扰后后台的梗塞大小限制效果,并研究过氧硝酸盐在这种现象中的累及。将大鼠喂养2%胆固醇或正常的饮食12 WK。梗塞大小由三苯基四唑氯化物染色在两组中分离的心脏测量,并进行30分钟的冠状动脉闭塞,然后120分钟再灌注或没有后处理方案诱导的10秒冠状动脉闭塞的10次循环闭塞和10次再灌注再灌注。后处理显着降低了常见性群体中的常见虫大小。在再灌注第5分钟测量时,在正常但不在胆固醇进料组中增加心脏3-硝基甲胺浓度(用于过氧硝酸盐形成的标记物)。接下来,我们测试了在单独的实验中涉及过氧硝酸盐的后后处理诱导的急性急性急性增加。后后台未能降低在摩染脂肪动物动物的过氧硝酸盐分解催化剂5,10,15,20-四 - [4-磺酰苯基苯基]-苯乙烯 - 铁[III](20mg / L)的存在下降低梗塞尺寸。我们得出结论,后后处理后过氧族酸的早期增加起在心脏保护作用中的作用。此外,高脂血症至少部分地通过后处理诱导的过氧硝酸盐形成的早期增加来阻断后处理的心脏保护作用。

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