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Resistance to diet-induced obesity in mice globally overexpressing OGH/GPB5

We identified a glycoprotein hormone beta-subunit (OGH, also called GPB5) that, as a heterodimer with the alpha-subunit GPA2, serves as a second ligand for the thyroid-stimulating hormone receptor. Mice in which the OGH gene is deleted (OGH(-/-)) are indistinguishable from WT littermates in body wei...

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Published in:Proceedings of the National Academy of Sciences - PNAS 2005-02, Vol.102 (7), p.2496-2501
Main Authors: Macdonald, L.E, Wortley, K.E, Gowen, L.C, Anderson, K.D, Murray, J.D, Poueymirou, W.T, Simmons, M.V, Barber, D, Valenzuela, D.M, Economides, A.N
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Language:English
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Summary:We identified a glycoprotein hormone beta-subunit (OGH, also called GPB5) that, as a heterodimer with the alpha-subunit GPA2, serves as a second ligand for the thyroid-stimulating hormone receptor. Mice in which the OGH gene is deleted (OGH(-/-)) are indistinguishable from WT littermates in body weight, response to high-fat diet, metabolic parameters, body composition, and insulin tolerance. Mice engineered to transgenically globally overexpress OGH (OGH-TG) develop approximately equal to 2-fold elevations in their basal thyroid levels and weigh slightly less than WT littermates despite increased food intake because of an increase in their metabolic rates. Moreover, when OGH-TG mice are challenged with a high-fat diet, they gain significantly less weight and body fat than their WT littermates. The OGH-TG mice also have reduced blood glucose, insulin, cholesterol, and triglycerides. In contrast to other approaches in which the thyroid axis is activated, OGH-TG mice exhibit only minor changes in heart rate and blood pressure. Our findings suggest that constitutive low-level activation of the thyroid axis (via OGH or other means) may provide a beneficial therapeutic approach for combating diet-induced obesity.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0409849102