4.7 Article

Sex differences in insulin resistance in GABAB1 knockout mice

期刊

LIFE SCIENCES
卷 92, 期 3, 页码 175-182

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.lfs.2012.11.007

关键词

GABAB receptors; Food intake; Insulin signaling; Akt activation; NPY expression

资金

  1. Consejo Nacional de Investigaciones Cientificas y Tecnicas, Argentina (CONICET) [363]
  2. Agencia Nacional de Promocion Cientifica y Tecnologica, Argentina (BID PICT) [0150, 00200]
  3. Universidad de Buenos Aires, Argentina (UBA) [M043]

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Aims: We have previously demonstrated that the absence of functional GABA B receptors (GABABRs) disturbs glucose homeostasis in GABAB1KO mice. The aim of this work was to extend our studies of these alterations in GABAB1KO mice and investigate the sexual differences therein. Main methods: Male and female, GABAB1KO and WT mice were used. Glucose and insulin tolerance tests (GTT and ITT), and insulin and glucagon secretion tests (IST and GST) were performed. Blood glucose, serum insulin and hyperglycemic hormones were determined, and HOMA-IR calculated. Skeletal muscle insulin receptor beta subunit (IR beta), insulin receptor substrates 1/2 (IRSI, IRS2) and hexokinase-II levels were determined by Western blot. Skeletal muscle insulin sensitivity was assessed by in vivo insulin-induced Akt phosphorylation (Western blot). Food intake and hypothalamic NPY mRNA expression (by qPCR) were also evaluated. Key findings: Fasted insulin and HOMA-IR were augmented in GABAB1KO males, with no alterations in females. Areas under the curve (AUC) for GTT and ITT were increased in GABABI KO mice of both genders, indicating compromised insulin sensitivity. No genotype differences were observed in IST, GST or in IRO, IRSI, IRS2 and hexokinase-II expression. Akt activation was severely impaired in GABABI KO males while no alterations were observed in females. GABAB1KO mice showed increased food intake and NPY expression. Significance: Glucose metabolism and energy balance disruptions were more pronounced in GABABI KO males, which develop peripheral insulin resistance probably due to augmented insulin secretion. Metabolic alterations in females were milder and possibly due to previously described reproductive disorders, such as persistent estrus. (C) 2012 Elsevier Inc. All rights reserved.

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