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ABSTRACT: Objective
We aimed to investigate the short and long-term metabolic consequences of IGF1R systemic gene deficiency in mice.Methods
UBC-CreERT2, Igf1rfl/fl mutant mice were used to suppress IGF1R signaling in adult tissues by inducing postnatal generalized Igf1r deletion with tamoxifen. Animals were analyzed at two different ages: i) 13-weeks old young mice, and ii) 12-months old middle-aged mice. In addition, the effects of 10 weeks-long high-fat diet (HFD) were investigated in middle-aged mice.Results
Young IGF1R-deficient mice were insulin-resistant, with high IGF1, growth hormone (GH) and IGFBP3, as well as low IGFBP2 circulating levels. Males also presented increased triglycerides in liver. In contrast, middle-aged mice did
SUBMITTER: Perez-Matute P
PROVIDER: S-EPMC9638844 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature