Gero 2017 IntechOpen

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Gero D (2023) Hyperglycemia-induced endothelial dysfunction. IntechOpen Chapter 8. http://dx.doi.org/10.5772/intechopen.71433.

Β» [file:///C:/Users/gnaigere/Downloads/Hyperglycemia-Induced_Endothelial_Dysfunction.pdf Open Access]

Gero D (2018) IntechOpen

Abstract: Glucose-induced endothelial dysfunction plays a fundamental role in the development of diabetic vascular complications and glycemic control (the foundation of diabetes care) provides limited protection against the cardiovascular complications. Therefore, iden- tification of novel drug targets and treatment approaches for diabetes complications represent a key direction of current pharmaceutical research. The β€œunifying theory” of hyperglycemia-induced endothelial cell injury organizes the events of cellular dysfunc- tion in a linear cascade and identifies mitochondrial superoxide generation as the trig- gering event of the injury. Exposure to high glucose concentration for long periods or repeated glycemic swings may induce changes in metabolic substrate availability and lead to mitochondrial hyperpolarization. Changes in the mitochondrial membrane poten- tial induce superoxide production by the electron transport chain and result in oxidative stress. Mitochondrial superoxide is also responsible for the induction of other sources of reactive oxygen species (ROS) within the cells, including advanced glycation end prod- ucts (AGEs) and the NADPH oxidase. Mitochondria also show morphological changes and impaired assembly of the respiratory complexes occurs, which results in cellular energy failure, cell senescence and vascular dysfunction. Current intervention strategies aim to inhibit the mitochondrial ROS production and novel therapeutic approaches are expected to provide valuable tools in diabetes therapy in the upcoming years.

β€’ Bioblast editor: Gnaiger E


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Enzyme: Complex II;succinate dehydrogenase 




Gero 2018 IntechOpen CORRECTION.png

Correction: FADH2 and Complex II

Ambiguity alert.png
FADH2 is shown as the substrate feeding electrons into Complex II (CII). This is wrong and requires correction - for details see Gnaiger (2024).
Gnaiger E (2024) Complex II ambiguities ― FADH2 in the electron transfer system. J Biol Chem 300:105470. https://doi.org/10.1016/j.jbc.2023.105470 - Β»Bioblast linkΒ«
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