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- W2893821012 abstract "Summary Patients with overnutrition, obesity, the atherometabolic syndrome, and type 2 diabetes mellitus exhibit imbalanced insulin action , also called pathway-selective insulin resistance. To control glycemia, they require hyperinsulinemia that then overdrives ERK and hepatic de-novo lipogenesis. We recently reported that NADPH oxidase-4 regulates balanced insulin action. Here, we show that NADPH oxidase-4 is part of a new limb of insulin signaling that we abbreviate “NSAPP” after its five major proteins. The NSAPP pathway is an oxide transport chain that begins when insulin stimulates NADPH oxidase-4 to generate . NADPH oxidase-4 hands to superoxide dismutase-3 for conversion into H 2 O 2 . The pathway ends when aquaporin-3 channels H 2 O 2 across the membrane to inactivate PTEN. Disruption of any component of the NSAPP chain, from NADPH oxidase-4 up to PTEN, leaves PTEN persistently active, thereby producing the same deadly pattern of imbalanced insulin action seen clinically. Unraveling the molecular basis for NSAPP dysfunction in overnutrition has now become a top priority." @default.
- W2893821012 created "2018-10-05" @default.
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- W2893821012 date "2018-09-29" @default.
- W2893821012 modified "2023-10-03" @default.
- W2893821012 title "An oxide transport chain essential for balanced insulin signaling" @default.
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- W2893821012 doi "https://doi.org/10.1101/430637" @default.
- W2893821012 hasPublicationYear "2018" @default.
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