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再灌注心肌中底物代谢的变化及过量脂肪酸的影响。

Changes in substrate metabolism and effects of excess fatty acids in reperfused myocardium.

作者信息

Liedtke A J, DeMaison L, Eggleston A M, Cohen L M, Nellis S H

机构信息

Section of Cardiology, University of Wisconsin, Madison 53792.

出版信息

Circ Res. 1988 Mar;62(3):535-42. doi: 10.1161/01.res.62.3.535.

Abstract

The purpose of these studies was to characterize the rates of fatty acid oxidation in reperfused myocardium and test the influence of excess fatty acids (FA) on mechanical function in the extracorporeally perfused, working swine heart model. Seventeen animals were prepared. Eight were untreated (LOW FA group; serum FA averaged 0.55 +/- 0.07 mumol/ml) and nine received a constant infusion of 10% Intralipid with heparin to raise serum FA to about 1.4 +/- 0.21 mumol/ml (HIGH FA group). Coronary flow in both groups was held at aerobic levels for an equilibrium period of 40 minutes, acutely reduced regionally in the anterior descending circulation by 60% for 45 minutes, and acutely restored to aerobic levels for 60-minute reflow. Appreciable mechanical depression (-47 delta% from aerobic values; p less than 0.01) during reperfusion was noted in both groups. This was associated with modest reductions in myocardial oxygen consumption (p less than 0.05) and losses of total tissue carnitine stores (p at least less than 0.02). Reperfused myocardium showed a strong preference for and aerobic use of FA during reflow such that 14CO2 production from labeled palmitate exceeded preischemic levels (+89 delta% in LOW FA hearts; +111 delta% in HIGH FA hearts). This suggested relative preservation of restoration of certain elements in mitochondrial function during reflow. The findings argue for uncoupling between substrate metabolism and energy production, accelerated but useless energy drainage, or some impairment between energy transfer and function of contractile proteins as possible explanations for the persistent depression of mechanical function (stunning) during reperfusion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

这些研究的目的是测定再灌注心肌中脂肪酸氧化的速率,并在体外灌注的工作猪心脏模型中测试过量脂肪酸(FA)对心脏机械功能的影响。准备了17只动物。8只未处理(低脂肪酸组;血清脂肪酸平均为0.55±0.07μmol/ml),9只持续输注含肝素的10%英脱利匹特,使血清脂肪酸升高至约1.4±0.21μmol/ml(高脂肪酸组)。两组的冠状动脉血流在有氧水平维持40分钟的平衡期,在前降支循环区域急性降低60%并持续45分钟,然后急性恢复到有氧水平进行60分钟的再灌注。两组在再灌注期间均出现明显的机械功能降低(相对于有氧值降低47%;p<0.01)。这与心肌耗氧量适度降低(p<0.05)和总组织肉碱储备减少(p至少<0.02)有关。再灌注心肌在再灌注期间对脂肪酸有强烈的偏好并进行有氧利用,以至于标记棕榈酸产生的14CO2超过缺血前水平(低脂肪酸组心脏中升高89%;高脂肪酸组心脏中升高111%)。这表明再灌注期间线粒体功能的某些元素相对得以保留或恢复。这些发现表明底物代谢与能量产生之间解偶联、能量消耗加速但无用,或者能量传递与收缩蛋白功能之间存在某种损害,可能是再灌注期间机械功能持续降低(心肌顿抑)的原因。(摘要截短于250字)

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