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Impact of mitochondrial ROS production on diabetic vascular complications.

Abstract
Vascular complications are the leading cause of morbidity and mortality in patients with diabetes. Four main molecular mechanisms have been implicated in glucose-mediated vascular disease. There are: glucose-induced activation of protein kinase C (PKC) isoforms; increased formation of glucose-derived advanced glycation end-products (AGE); increased glucose flux through the aldose reductase pathway; and increased production of reactive oxygen species (ROS). Here we demonstrate that hyperglycemia-induced production of ROS is abrogated by inhibitors of mitochondrial metabolism, or by overexpression of uncoupling protein-1 or manganese superoxide dismutase. Normalization of mitochondrial ROS production by each of these agents prevents glucose-induced activation of PKC, formation of AGE, and accumulation of sorbitol in bovine vascular endothelial cells. We also claim that 8-hydroxydeoxyguanosine, which represents mitochondrial oxidative damage was elevated in patients with either retinopathy, albuminuria or increased intima-media thickness of carotid arteries. These results suggest that hyperglycemia induces mitochondrial ROS production, and which can associate to the pathogenesis of diabetic vascular complications.
AuthorsTakeshi Nishikawa, Daisuke Kukidome, Kazuhiro Sonoda, Kazuo Fujisawa, Takako Matsuhisa, Hiroyuki Motoshima, Takeshi Matsumura, Eiichi Araki
JournalDiabetes research and clinical practice (Diabetes Res Clin Pract) Vol. 77 Suppl 1 Pg. S41-5 (Sep 2007) ISSN: 0168-8227 [Print] Ireland
PMID17452060 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Reactive Oxygen Species
  • 8-oxo-7-hydrodeoxyguanosine
  • Deoxyguanosine
Topics
  • Citric Acid Cycle
  • Deoxyguanosine (analogs & derivatives, metabolism)
  • Diabetic Angiopathies (physiopathology)
  • Humans
  • Mitochondria (physiology)
  • Models, Biological
  • Reactive Oxygen Species (metabolism)

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