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The Role of NADPH oxidase 2 (NOX2) in High-Fat Diet-Induced Adiposopathy and Brain Dysfunction in a Mouse Model

Obesity can have numerous detrimental consequences, namely metabolic syndrome, type 2 diabetes, cardiovascular disease, cancer, and Alzheimers disease. The pathogenesis and physiologic consequences of obesity are unknown, but they are often associated with increased inflammation and oxidative stress in both the body and in the brain. One factor that has been implicated in causing inflammation associated with a high fat diet is the enzyme NADPH oxidase, or NOX, specifically the subunit NOX2. Two studies were performed in order to assess the effects of a high fat diet in combination with a universal NOX2 deficiency and a NOX2 deficiency targeted to macrophages. The results of the first study indicate that the NOX2 knockout (NOX2KO) mice on a high fat diet do not experience all the deleterious metabolic and inflammatory effects in the body and brain to the same degree as wild-type mice. This suggests that a deficiency in NOX2 does offer protection from some of the deleterious effects of a high fat diet. It was also determined from the first study that NOX2 expression is localized to macrophages in the visceral adipose tissue. In order to target these macrophages, a second study was conducted. For this second study, a mouse model was genetically engineered with the intent of inhibiting NOX2 solely within macrophages. Similar to the first study, these macrophage-deficient NOX2 knockout (macNOX2KO) mice were placed on a high fat along with the NOX2-flox wild-type (WT-FL) mice. The results suggest that the macrophage-deficient NOX2 knockout mice were protected from the deleterious effects of a high fat diet.
In summary, the deletion of NOX2 appears to offer a protective benefit against the deleterious effects of obesity in the context of a high fat diet. Specifically, the deletion of NOX2 in macrophages also offers this protection with the added benefit of targeting the deletion so as to not affect NOX2 functioning in other cells in the body.

Identiferoai:union.ndltd.org:LSU/oai:etd.lsu.edu:etd-06272016-140723
Date14 July 2016
CreatorsPepping, Jennifer Kathleen
ContributorsBruce-Keller, Annadora, Stout, Rhett Whitman, Baker, David George, Keller, Jeffrey N, Guerrero-Plata, Antonieta, Langohr, Ingeborg
PublisherLSU
Source SetsLouisiana State University
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lsu.edu/docs/available/etd-06272016-140723/
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