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Low intrinsic aerobic exercise capacity and systemic insulin resistance are not associated with changes in myocardial substrate oxidation or insulin sensitivity

机译:低的固有有氧运动能力和全身性胰岛素抵抗与心肌底物氧化或胰岛素敏感性的变化无关

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In patients, inactivity, obesity and insulin resistance are associated with increased incidence of heart failure. Rats selectively bred for low (LCR) intrinsic aerobic exercise capacity show signs of the metabolic syndrome including insulin resistance, compared to their counterparts bred for high intrinsic aerobic capacity (HCR). We reasoned that systemic insulin resistance in LCR should translate to impaired substrate oxidation and reduced insulin sensitivity in the heart. Isolated hearts were perfused in the working mode to analyze cardiac function, substrate oxidation patterns, insulin response, and oxygen consumption. After 22 generations of selective breeding, LCR displayed reduction of exercise capacity (LCR vs. HCR: distance 280 ± 12 vs. 1,968 ± 63 m, time 19.5 ± 0.6 vs. 71.7 ± 1.4 min, speed 19.2 ± 0.3 vs. 45.3 ± 0.7 m/min; all p < 0.05). At 21 weeks, body weight (+34%), tibia length (+6%), heart weight (+31%), and heart weight to tibia length ratio (+24%; all p < 0.05) were increased. LCR display higher random glucose, higher fasting glucose, and higher insulin levels in serum than HCR indicating the presence of insulin resistance in LCR. Here, in contrast, isolated hearts showed no differences in glucose (0.22 ± 0.02 μmol/min/g dry) or fatty acid oxidation (0.79 ± 0.10 μmol/min/g dry), oxygen consumption (28.3 ± 4.1 nmol O2/min/g dry) or cardiac power (18.6 ± 1.6 mW/g dry). Furthermore, sensitivity to insulin (Δglucose oxidation: +0.57 ± 0.095 μmol/min/g dry) was not different between the two populations. Low intrinsic exercise capacity and systemic insulin resistance in rats are not associated with changes in cardiac substrate oxidation, insulin sensitivity, oxygen consumption, or cardiac function. The lack of cardiac insulin resistance in the face of systemic insulin resistance supports a concept of different pathomechanisms for these two conditions.
机译:在患者中,缺乏运动,肥胖和胰岛素抵抗与心力衰竭的发生率增加有关。与为高固有有氧运动能力(HCR)繁殖的大鼠相比,选择性为低(LCR)固有有氧运动能力培养的大鼠表现出包括胰岛素抵抗在内的代谢综合症。我们认为LCR中的全身胰岛素抵抗应转化为受损的底物氧化并降低心脏中的胰岛素敏感性。在工作模式下对孤立的心脏进行灌注,以分析心脏功能,底物氧化模式,胰岛素反应和耗氧量。经过22代的选择性繁殖,LCR显示出运动能力下降(LCR vs.HCR:距离280±12 vs.1,968±63 m,时间19.5±0.6 vs.71.7±1.4 min,速度19.2±0.3 vs.45.3±0.7 m / min;所有p <0.05)。在21周时,体重(+ 34%),胫骨长度(+ 6%),心脏重量(+ 31%)和心脏重量与胫骨长度之比(+ 24%;所有p <0.05)均增加。与HCR相比,LCR在血清中显示出更高的随机葡萄糖,更高的空腹血糖和更高的胰岛素水平,表明LCR中存在胰岛素抵抗。相比之下,在这里,离体的心脏在葡萄糖(0.22±0.02μmol/ min / g干燥)或脂肪酸氧化(0.79±0.10μmol/ min / g干燥),氧消耗(28.3±4.1 nmol O 2 / min / g干燥)或心律(18.6±1.6 mW / g干燥)。此外,两个人群对胰岛素的敏感性(Δ葡萄糖氧化:+0.57±0.095μmol/ min / g干燥)无差异。大鼠低的固有运动能力和全身性胰岛素抵抗与心脏底物氧化,胰岛素敏感性,耗氧量或心脏功能的变化无关。面对全身性胰岛素抵抗,缺乏心脏胰岛素抵抗支持了针对这两种情况的不同病理机制的概念。

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