Succinate in ischemia: Where does it come from?

被引:39
|
作者
Chinopoulos, Christos [1 ]
机构
[1] Semmelweis Univ, Dept Med Biochem, Tuzolto St 37-47, H-1094 Budapest, Hungary
关键词
Fumarate; Hypoxia; Anoxia; Substrate-level phosphorylation; TCA cycle; Succinate dehydrogenase; SUBSTRATE-LEVEL PHOSPHORYLATION; CITRIC-ACID CYCLE; MITOCHONDRIAL ENERGY-METABOLISM; CATALYTIC ELECTRON-TRANSPORT; FUMARATE REDUCTASE-ACTIVITY; ANAEROBIC RAT-HEART; COMPLEX II; NUCLEOSIDE DIPHOSPHOKINASE; UBIQUINONE REDUCTASE; REPERFUSION INJURY;
D O I
10.1016/j.biocel.2019.105580
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During tissue ischemia succinate accumulates. Herein, literature spanning the past nine decades is reviewed leaning towards the far greater role of Krebs cycle's canonical activity yielding succinate through alpha-ketoglutarate - > succinyl-CoA - > succinate even in hypoxia, as opposed to reversal of succinate dehydrogenase. Furthermore, the concepts of i) a diode-like property of succinate dehydrogenase rendering it difficult to reverse, and ii) the absence of mammalian mitochondrial quinones exhibiting redox potentials in the [-60, -80] mV range needed for fumarate reduction, are discussed. Finally, it is emphasized that a "fumarate reductase" enzyme entity reducing fumarate to succinate found in some bacteria and lower eukaryotes remains to be discovered in mammalian mitochondria.
引用
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页数:6
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