Janero D R, Hreniuk D, Sharif H M
Research Department, Ciba-Geigy Corporation, Summit, New Jersey 07901.
Am J Physiol. 1994 Jan;266(1 Pt 1):C179-88. doi: 10.1152/ajpcell.1994.266.1.C179.
Hydrogen peroxide (H2O2) may incite cardiac ischemia-reperfusion injury. We evaluate herein the influence of H2O2-induced oxidative stress on heart muscle hexose metabolism in cultured neonatal rat cardiomyocytes, which have a substrate preference for carbohydrate. Cardiomyocyte exposure to 50 microM-1.0 mM bolus H2O2 transiently activated the pentose phosphate cycle and thereafter inhibited cellular glucose oxidation and glycolysis. These metabolic derangements were nonperoxidative in nature (as assessed in alpha-tocopherol-loaded cells) and occurred without acute change in cardiomyocyte hexose transport or glucose/glycogen reserves. Glycolytic inhibition was supported by the rapid, specific inactivation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The degree of GAPDH inhibition correlated directly with the magnitude of the oxidative insult and was independent of both metal-catalyzed H2O2 reduction to free radicals and lipid peroxidation. Severe GAPDH inhibition was required for a rate-limiting effect on glycolytic flux. Cardiomyocyte pyruvate dehydrogenase was also inhibited by H2O2 overload, but to a lesser degree than GAPDH such that entry of hexose-derived acetyl units into the tricarboxylic acid cycle was not as restrictive as GAPDH inactivation to glycolytic ATP production. An increase in phosphofructokinase activity accompanied GAPDH inactivation, leading to the production and accumulation of glycolytic sugar phosphates at the expense of ATP equivalents. Cardiomyocyte treatment with iodoacetate or 2-deoxyglucose indicated that GAPDH inactivation/glycolytic blockade could account for approximately 50% of the maximal ATP loss following H2O2 overload. Partial restoration of GAPDH activity after a brief H2O2 "pulse" afforded some ATP recovery. These data establish that specific aspects of heart muscle hexose catabolism are H2O2-sensitive injury targets. The biochemical pathology of H2O2 overload on cardiomyocyte carbohydrate metabolism has implications for post-ischemic cardiac bioenergetics and function.
过氧化氢(H2O2)可能引发心脏缺血再灌注损伤。在此,我们评估H2O2诱导的氧化应激对培养的新生大鼠心肌细胞中心肌己糖代谢的影响,这些细胞对碳水化合物具有底物偏好。心肌细胞暴露于50微摩尔/升至1.0毫摩尔/升的一次性H2O2中会短暂激活磷酸戊糖循环,随后抑制细胞葡萄糖氧化和糖酵解。这些代谢紊乱本质上是非过氧化性的(在加载α-生育酚的细胞中评估),并且在心肌细胞己糖转运或葡萄糖/糖原储备无急性变化的情况下发生。糖酵解抑制由甘油醛-3-磷酸脱氢酶(GAPDH)的快速、特异性失活所支持。GAPDH抑制程度与氧化损伤程度直接相关,且与金属催化H2O2还原为自由基以及脂质过氧化均无关。对糖酵解通量产生限速作用需要严重的GAPDH抑制。心肌细胞丙酮酸脱氢酶也会被H2O2过载抑制,但程度低于GAPDH,因此己糖衍生的乙酰单位进入三羧酸循环的限制程度不如GAPDH失活对糖酵解ATP产生的限制程度大。磷酸果糖激酶活性增加伴随着GAPDH失活,导致糖酵解糖磷酸酯的产生和积累,以消耗ATP当量为代价。用碘乙酸盐或2-脱氧葡萄糖处理心肌细胞表明,GAPDH失活/糖酵解阻断可解释H2O2过载后最大ATP损失的约50%。短暂的H2O2“脉冲”后GAPDH活性的部分恢复使ATP有所恢复。这些数据表明,心肌己糖分解代谢的特定方面是H2O2敏感的损伤靶点。H2O2过载对心肌细胞碳水化合物代谢的生化病理学对缺血后心脏生物能量学和功能具有影响。