[不同缺氧-复氧持续时间大鼠肝脏线粒体的能量和抗氧化状态]。

O. Gonchar, V. Nosar, L. V. Bratus, I. Tymchenko, N. Steshenko, I. Mankovska
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引用次数: 3

摘要

研究了缺氧复氧不同持续时间(1、3、7、14天)大鼠肝脏线粒体中抗自由基(MnSOD)、谷胱甘肽依赖(谷胱甘肽过氧化物酶、谷胱甘肽还原酶)和谷胱甘肽生成NADP +(异柠檬酸脱氢酶)酶活性和蛋白表达的动态变化。大鼠血液中皮质酮浓度的变化与大鼠肝脏线粒体能量代谢、促氧化平衡和抗氧化平衡的变化相对应。研究表明,短期(1天)缺氧再氧化(气体混合物中含有5% O2)导致大鼠肝脏线粒体中皮质酮浓度升高,氧化过程和能量代谢显著激活,其强度在第3天减弱。长期缺氧-再氧化(7-14天)导致机体适应能力逐渐耗竭,表现为血液皮质酮浓度显著下降、脂质过氧化二次产物含量增加、促氧化和抗氧化反应失衡以及肝细胞线粒体能量容量降低。结果表明,在整个实验期间,谷胱甘肽过氧化物酶蛋白表达量和酶活性不断升高,且与H₂O₂水平呈正相关。Mn-SOD蛋白含量和酶活性在试验前7天较低,随后各天呈上升趋势,至第14天达到对照水平。在长时间缺氧-复氧过程中,谷胱甘肽过氧化物酶、谷胱甘肽还原酶和NADP+依赖的异柠檬酸脱氢酶活性增加,表明谷胱甘肽和nadph生成酶积极参与抗氧化保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[ENERGETIC AND ANTIOXIDANT STATUS OF RAT LIVER MITOCHONDRIA DURING HYPOXIA-REOXYGENATION OF DIFFERENT DURATION].
Dynamics of changes in activity and protein expression of antiradical (MnSOD), glutathione-dependent (glutathione peroxidase, glutathione reductase) and NADP⁺-generated (isocitrate dehydrogenase) enzymes as well as in the energy metabolism indeces in rat liver mitochondria under hypoxia- reoxygenation of different duration (1, 3, 7 14 days) were studied. Prolonged hypoxia-reoxygenation was characterized by phase changes of the corticosterone concentration in rat blood, which corresponded to the changes in energy metabolism as well as in pro- and antioxidant balance in rat liver mitochondria. It has been shown that short-term (1 day) hypoxia-reoxygenation (5% O2 in the gas mixture) led to an increase in the blood corticosterone concentration and a significant activation of oxidative processes and energy metabolism in rat liver mitochondria, the intensity of which was reduced to 3rd day. Long- term hypoxia--reoxygenation (7-14th days) led to the gradual depletion of the organism adaptive capabilities, as evidenced by a significant decline in the blood corticosterone concentration, an increase in the content of secondary products of lipid peroxidation, an imbalance in pro- and antioxidant reactions and reduction of energy capacity in liver cells mitochondria. It has been shown that the glutathione peroxidase protein expression and enzymatic activity increased constantly during the whole experimental period and correlated positively with the level of H₂O₂. The amount of Mn-SOD protein as well as it's enzymatic activity was lower in the first seven days of experiment, and it was increased in consequent days up to the control level on 14thday. Increased activity of glutathione peroxidase, glutathione reductase and NADP+⁺dependent isocitrate dehydrogenase during prolonged hypoxia - eoxygenation indicates that glutathione- and NADPH-generating enzymes, were actively involved in the antioxidant protect.
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