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Glucose‐dependent insulinotropic polypeptide deficiency reduced fat accumulation and insulin resistance, but deteriorated bone loss in ovariectomized mice

Given the established roles of glucose‐dependent insulinotropic polypeptide (GIP) in promoting fat storage and bone formation, we assessed the contribution of GIP to obesity and osteopenia in ovariectomized mice with a gene encoding green fluorescent protein (GFP) inserted into the GIP locus, in whi...

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Detalles Bibliográficos
Autores principales: Shimazu‐Kuwahara, Satoko, Kanemaru, Yoshinori, Harada, Norio, Ikeguchi, Eri, Ueda, Yohei, Yamane, Shunsuke, Murata, Yuki, Yasoda, Akihiro, Kieffer, Timothy J, Inagaki, Nobuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6626948/
https://www.ncbi.nlm.nih.gov/pubmed/30451382
http://dx.doi.org/10.1111/jdi.12978
Descripción
Sumario:Given the established roles of glucose‐dependent insulinotropic polypeptide (GIP) in promoting fat storage and bone formation, we assessed the contribution of GIP to obesity and osteopenia in ovariectomized mice with a gene encoding green fluorescent protein (GFP) inserted into the GIP locus, in which GIP was either reduced (GIP(gfp/+)) or absent (GIP(gfp/gfp)). In GIP(gfp/gfp) mice, weight gain, subcutaneous and visceral fat mass were reduced, and glucose intolerance was improved compared with wild‐type mice with the same magnitude of insulin responses. Cancellous bone mineral density and bone cortical thickness were reduced in GIP(gfp/gfp) mice compared with wild‐type mice. In GIP(gfp/+) mice, weight gain, glucose intolerance and cancellous bone mineral density were not different from that of wild‐type mice. These results indicate that the total elimination of GIP ameliorates weight gain and adiposity in ovariectomized mice, but it enhances osteopenia, particularly in cancellous bone by partly suppressing bone formation.