Lukianova L D
Patol Fiziol Eksp Ter. 2011 Jan-Mar(1):3-19.
A bioenergetic mechanism for development of urgent and long-term adaptation to hypoxia is considered. Hypoxia induces reprogramming of respiratory chain function and switching from oxidation of NAD-related substrates (complex I) to succinate oxidation (complex II). Transient, reversible, compensatory activation of respiratory chain complex II is a major mechanism of urgent adaptation to hypoxia necessary for 1) succinate-related energy synthesis in conditions of oxygen deficiency and formation of urgent resistance in the body; 2) succinate-related stabilization of HIF-1alpha and initiation of its transcriptional activity related with formation of long-term adaptation; 3) succinate-related activation of a succinate-specific receptor CPR91. Therefore succinate is a signaling molecule, which effects are realized at three levels in hypoxia, intramitochondrial, intracellular and intercellular. Tactics and strategy for the antihypoxic defense and development of antihypoxants with energotropic action are considered.
本文探讨了机体对缺氧产生急性和长期适应性的生物能量机制。缺氧会引发呼吸链功能的重编程,并促使呼吸从依赖NAD的底物氧化(复合体I)转变为琥珀酸氧化(复合体II)。呼吸链复合体II的短暂、可逆且具有代偿性的激活是机体对缺氧产生急性适应性的主要机制,这一机制对于以下几点至关重要:1)在缺氧条件下通过琥珀酸进行能量合成,并在体内形成急性耐受性;2)通过琥珀酸实现HIF-1α的稳定,并启动与长期适应性形成相关的转录活性;3)通过琥珀酸激活特定的琥珀酸受体CPR91。因此,琥珀酸是一种信号分子,其作用在缺氧的三个层面得以体现,即线粒体内、细胞内和细胞间。文中还讨论了抗缺氧防御的策略以及具有能量调节作用的抗缺氧剂的研发。