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Fatty Acid Oxidation and Mitochondrial Morphology Changes as Key Modulators of the Affinity for ADP in Rat Heart Mitochondria

机译:脂肪酸氧化和线粒体形态变化作为大鼠心脏线粒体ADP亲和力的关键调节因子

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摘要

Fatty acids are the main respiratory substrates important for cardiac function, and their oxidation is altered during various chronic disorders. We investigated the mechanism of fatty acid–oxidation-induced changes and their relations with mitochondrial morphology and ADP/ATP carrier conformation on the kinetics of the regulation of mitochondrial respiration in rat skinned cardiac fibers. Saturated and unsaturated, activated and not activated, long and medium chain, fatty acids similarly decreased the apparent K . Addition of 5% dextran T-70 to mimic the oncotic pressure of the cellular cytoplasm markedly increased the low apparent K value of mitochondria in cardiac fibers respiring on palmitoyl- -carnitine or octanoyl- -carnitine, but did not affect the high apparent K of mitochondria respiring on pyruvate and malate. Electron microscopy revealed that palmitoyl- -carnitine oxidation-induced changes in the mitochondrial ultrastructure (preventable by dextran) are similar to those induced by carboxyatractyloside. Our data suggest that a fatty acid oxidation-induced conformational change of the adenosine diphosphate (ADP)/adenosine triphosphate (ATP) carrier (M-state to C-state, condensed to orthodox mitochondria) may affect the oxidative phosphorylation affinity for ADP.
机译:脂肪酸是对心脏功能重要的主要呼吸底物,脂肪酸的氧化在各种慢性疾病中会发生改变。我们研究了脂肪酸氧化诱导的变化的机制及其与线粒体形态和ADP / ATP载体构象的关系,这些线粒体对大鼠皮肤心脏纤维线粒体呼吸调节的动力学。饱和和不饱和,活化和未活化的长链和中链脂肪酸同样降低了表观K。添加5%的葡聚糖T-70以模拟细胞质的渗透压,显着增加了在棕榈酰--肉碱或辛酰基--肉碱上呼吸的心脏纤维中线粒体的低表观K值,但并不影响线粒体的高表观K值。线粒体在丙酮酸和苹果酸上呼吸。电子显微镜显示,棕榈酰-肉碱氧化诱导的线粒体超微结构变化(右旋糖酐可预防)与羧基白术苷诱导的变化相似。我们的数据表明,脂肪酸氧化诱导的二磷酸腺苷(ADP)/三磷酸腺苷(ATP)载体的构象变化(M-状态变为C-状态,浓缩为正弦线粒体)可能会影响ADP的氧化磷酸化亲和力。

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