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S3QELs protect against diet-induced intestinal barrier dysfunction.

Mark A WatsonBlaine PattavinaTyler A U HilsabeckJose Lopez-DominguezPankaj KapahiMartin D Brand
Published in: Aging cell (2021)
The underlying causes of aging remain elusive, but may include decreased intestinal homeostasis followed by disruption of the intestinal barrier, which can be mimicked by nutrient-rich diets. S3QELs are small-molecule suppressors of site IIIQo electron leak; they suppress superoxide generation at complex III of the mitochondrial electron transport chain without inhibiting oxidative phosphorylation. Here we show that feeding different S3QELs to Drosophila on a high-nutrient diet protects against greater intestinal permeability, greater enterocyte apoptotic cell number, and shorter median lifespan. Hif-1α knockdown in enterocytes also protects, and blunts any further protection by S3QELs. Feeding S3QELs to mice on a high-fat diet also protects against the diet-induced increase in intestinal permeability. Our results demonstrate by inference of S3QEL use that superoxide produced by complex III in enterocytes contributes to diet-induced intestinal barrier disruption in both flies and mice.
Keyphrases
  • high fat diet
  • small molecule
  • oxidative stress
  • insulin resistance
  • adipose tissue
  • physical activity
  • cell death
  • high fat diet induced
  • hydrogen peroxide
  • skeletal muscle