Chinopoulos 2013 J Neurosci Res: Difference between revisions

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|abstract=The citric acid cycle forms a major metabolic hub and as such it is involved in many disease states involving energetic imbalance. In spite of the fact that it is being branded as a "cycle", during hypoxia, when the electron transport chain does not oxidize reducing equivalents, segments of this metabolic pathway remain operational but exhibit opposing directionalities. This serves the purpose of harnessing high-energy phosphates through matrix substrate-level phosphorylation in the absence of oxidative phosphorylation. In this Mini-Review, these segments are appraised, pointing to the critical importance of the ฮฑ-ketoglutarate dehydrogenase complex dictating their directionalities.
|abstract=The citric acid cycle forms a major metabolic hub and as such it is involved in many disease states involving energetic imbalance. In spite of the fact that it is being branded as a "cycle", during hypoxia, when the electron transport chain does not oxidize reducing equivalents, segments of this metabolic pathway remain operational but exhibit opposing directionalities. This serves the purpose of harnessing high-energy phosphates through matrix substrate-level phosphorylation in the absence of oxidative phosphorylation. In this Mini-Review, these segments are appraised, pointing to the critical importance of the ฮฑ-ketoglutarate dehydrogenase complex dictating their directionalities.
|keywords=TCA cycle
|keywords=TCA cycle
<br>
|editor=Cardoso LHD
|editor=Cardoso LHD
|mipnetlab=HU Budapest Chinopoulos C
|mipnetlab=HU Budapest Chinopoulos C
}}
}}
[[File:Chinopoulos 2013 J Neurosci Res CORRECTION.png|left|300px]]
''Comment'': FAD is shown as FAD<sup>+</sup> - possibly by copying from NAD<sup>+</sup>. But FAD is neither charged nor a co-substrate comparable to NAD<sup>+</sup>, but it is a covalently bound prosthetic group in CII ([[Gnaiger 2023 MitoFit CII]]).
{{Labeling
{{Labeling
|injuries=Hypoxia
|injuries=Hypoxia
|additional=MitoFit2022rTCA
|additional=MitoFit2022rTCA
}}
}}

Revision as of 14:49, 4 August 2023

Publications in the MiPMap
Chinopoulos C (2013) Which way does the citric acid cycle turn during hypoxia? The critical role of ฮฑ-ketoglutarate dehydrogenase complex. J Neurosci Res 91:1030-43.

ยป PMID: 23378250 Open Access

Chinopoulos Christos (2013) J Neurosci Res

Abstract: The citric acid cycle forms a major metabolic hub and as such it is involved in many disease states involving energetic imbalance. In spite of the fact that it is being branded as a "cycle", during hypoxia, when the electron transport chain does not oxidize reducing equivalents, segments of this metabolic pathway remain operational but exhibit opposing directionalities. This serves the purpose of harnessing high-energy phosphates through matrix substrate-level phosphorylation in the absence of oxidative phosphorylation. In this Mini-Review, these segments are appraised, pointing to the critical importance of the ฮฑ-ketoglutarate dehydrogenase complex dictating their directionalities. โ€ข Keywords: TCA cycle
โ€ข Bioblast editor: Cardoso LHD โ€ข O2k-Network Lab: HU Budapest Chinopoulos C

Chinopoulos 2013 J Neurosci Res CORRECTION.png

Comment: FAD is shown as FAD+ - possibly by copying from NAD+. But FAD is neither charged nor a co-substrate comparable to NAD+, but it is a covalently bound prosthetic group in CII (Gnaiger 2023 MitoFit CII).

Labels:

Stress:Hypoxia 





MitoFit2022rTCA 

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