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Whitening and Impaired Glucose Utilization of Brown Adipose Tissue in a Rat Model of Type 2 Diabetes Mellitus

Brown adipose tissue (BAT) is an attractive therapeutic target to combat diabetes and obesity due to its ability to increase glucose expenditure. In a genetic rat model (ZDF fa/fa) of type-2 diabetes and obesity, we aimed to investigate glucose utilization of BAT by (18)F-FDG PET imaging. Male Zucke...

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Detalles Bibliográficos
Autores principales: Lapa, Constantin, Arias-Loza, Paula, Hayakawa, Nobuyuki, Wakabayashi, Hiroshi, Werner, Rudolf A., Chen, Xinyu, Shinaji, Tetsuya, Herrmann, Ken, Pelzer, Theo, Higuchi, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711946/
https://www.ncbi.nlm.nih.gov/pubmed/29196742
http://dx.doi.org/10.1038/s41598-017-17148-w
Descripción
Sumario:Brown adipose tissue (BAT) is an attractive therapeutic target to combat diabetes and obesity due to its ability to increase glucose expenditure. In a genetic rat model (ZDF fa/fa) of type-2 diabetes and obesity, we aimed to investigate glucose utilization of BAT by (18)F-FDG PET imaging. Male Zucker diabetic fatty (ZDF) and Male Zucker lean (ZL) control rats were studied at 13 weeks. Three weeks prior to imaging, ZDF rats were randomized into a no-restriction (ZDF-ND) and a mild calorie restriction (ZDF-CR) group. Dynamic (18)F-FDG PET using a dedicated small animal PET system was performed under hyperinsulinemic-euglycemic clamp. (18)F-FDG PET identified intense inter-scapular BAT glucose uptake in all ZL control rats, while no focally increased (18)F-FDG uptake was detected in all ZDF-ND rats. Mild but significant improved BAT tracer uptake was identified after calorie restriction in diabetic rats (ZDF-CR). The weight of BAT tissue and fat deposits were significantly increased in ZDF-CR and ZDF-ND rats as compared to ZL controls, while UCP-1 and mitochondrial concentrations were significantly decreased. Whitening and severely impaired insulin-stimulated glucose uptake in BAT was confirmed in a rat model of type-2 diabetes. Additionally, calorie restriction partially restored the impaired BAT glucose uptake.