Loss of glyoxalase 2 alters the glucose metabolism in zebrafish

Glyoxalase 2 is the second enzyme of the glyoxalase system, catalyzing the detoxification of methylglyoxal to d-lactate via SD-Lactoylglutathione. Recent in vitro studies have suggested Glo2 as a regulator of glycolysis, but if Glo2 regulates glucose homeostasis and related organ specific functions...

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Main Authors: Tabler, Christoph Tobias (Author) , Lodd, Elisabeth (Author) , Bennewitz, Katrin (Author) , Heim, Chiara (Author) , Erben, Vanessa (Author) , Schröder, Hannes (Author) , Poth, Tanja (Author) , Fleming, Thomas (Author) , Morgenstern, Jakob (Author) , Haußer-Siller, Ingrid (Author) , Sticht, Carsten (Author) , Poschet, Gernot (Author) , Szendrödi, Julia (Author) , Nawroth, Peter Paul (Author) , Kroll, Jens (Author)
Format: Article (Journal)
Language:English
Published: 2023
In: Redox Biology
Year: 2023, Volume: 59, Pages: 1-15
ISSN:2213-2317
DOI:10.1016/j.redox.2022.102576
Online Access:Resolving-System, Volltext: https://doi.org/10.1016/j.redox.2022.102576
Verlag, Volltext: https://www.sciencedirect.com/science/article/pii/S2213231722003482
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Author Notes:Christoph Tobias Tabler, Elisabeth Lodd, Katrin Bennewitz, Chiara Simone Middel, Vanessa Erben, Hannes Ott, Tanja Poth, Thomas Fleming, Jakob Morgenstern, Ingrid Hausser, Carsten Sticht, Gernot Poschet, Julia Szendroedi, Peter Paul Nawroth, Jens Kroll

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520 |a Glyoxalase 2 is the second enzyme of the glyoxalase system, catalyzing the detoxification of methylglyoxal to d-lactate via SD-Lactoylglutathione. Recent in vitro studies have suggested Glo2 as a regulator of glycolysis, but if Glo2 regulates glucose homeostasis and related organ specific functions in vivo has not yet been evaluated. Therefore, a CRISPR-Cas9 knockout of glo2 in zebrafish was created and analyzed. Consistent with its function in methylglyoxal detoxification, SD-Lactoylglutathione, but not methylglyoxal accumulated in glo2−/− larvae, without altering the glutathione metabolism or affecting longevity. Adult glo2−/− livers displayed a reduced hexose concentration and a reduced postprandial P70-S6 kinase activation, but upstream postprandial AKT phosphorylation remained unchanged. In contrast, glo2−/− skeletal muscle remained metabolically intact, possibly compensating for the dysfunctional liver through increased glucose uptake and glycolytic activity. glo2−/− zebrafish maintained euglycemia and showed no damage of the retinal vasculature, kidney, liver and skeletal muscle. In conclusion, the data identified Glo2 as a regulator of cellular energy metabolism in liver and skeletal muscle, but the redox state and reactive metabolite accumulation were not affected by the loss of Glo2. 
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