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GABAB1 基因敲除小鼠胰岛素抵抗的性别差异。

Sex differences in insulin resistance in GABAB1 knockout mice.

机构信息

Instituto de Biología y Medicina Experimental-CONICET, Buenos Aires, Argentina.

出版信息

Life Sci. 2013 Feb 27;92(3):175-82. doi: 10.1016/j.lfs.2012.11.007. Epub 2012 Nov 20.

Abstract

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 β subunit (IRβ), insulin receptor substrates 1/2 (IRS1, 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 GABAB1KO mice of both genders, indicating compromised insulin sensitivity. No genotype differences were observed in IST, GST or in IRβ, IRS1, IRS2 and hexokinase-II expression. Akt activation was severely impaired in GABAB1KO 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 GABAB1KO 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.

摘要

目的

我们之前已经证明,功能性 GABA B 受体 (GABABRs) 的缺失会扰乱 GABAB1KO 小鼠的葡萄糖稳态。本研究旨在扩展我们对 GABAB1KO 小鼠这些改变的研究,并探讨其中的性别差异。

方法

使用雄性和雌性 GABAB1KO 和 WT 小鼠。进行葡萄糖和胰岛素耐量试验(GTT 和 ITT)以及胰岛素和胰高血糖素分泌试验(IST 和 GST)。测定血糖、血清胰岛素和高血糖激素,并计算 HOMA-IR。通过 Western blot 测定骨骼肌胰岛素受体 β 亚基(IRβ)、胰岛素受体底物 1/2(IRS1、IRS2)和己糖激酶-II 水平。通过体内胰岛素诱导的 Akt 磷酸化(Western blot)评估骨骼肌胰岛素敏感性。还评估了食物摄入量和下丘脑 NPY mRNA 表达(通过 qPCR)。

主要发现

禁食胰岛素和 HOMA-IR 在 GABAB1KO 雄性中增加,而在雌性中没有变化。两性 GABAB1KO 小鼠的 GTT 和 ITT 曲线下面积(AUC)增加,表明胰岛素敏感性受损。在 IST、GST 或 IRβ、IRS1、IRS2 和己糖激酶-II 表达中没有观察到基因型差异。Akt 激活在 GABAB1KO 雄性中严重受损,而在雌性中没有观察到变化。GABAB1KO 小鼠表现出增加的食物摄入和 NPY 表达。

意义

葡萄糖代谢和能量平衡的紊乱在 GABAB1KO 雄性中更为明显,它们可能由于胰岛素分泌增加而发展为外周胰岛素抵抗。女性的代谢改变较轻,可能是由于之前描述的生殖障碍,如持续发情。

相似文献

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Sex differences in insulin resistance in GABAB1 knockout mice.GABAB1 基因敲除小鼠胰岛素抵抗的性别差异。
Life Sci. 2013 Feb 27;92(3):175-82. doi: 10.1016/j.lfs.2012.11.007. Epub 2012 Nov 20.
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Postnatal development of the endocrine pancreas in mice lacking functional GABAB receptors.功能性 GABAB 受体缺失小鼠的胰腺内分泌部的产后发育。
Am J Physiol Endocrinol Metab. 2013 May 15;304(10):E1064-76. doi: 10.1152/ajpendo.00569.2012. Epub 2013 Mar 26.
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GABAB receptors and glucose homeostasis: evaluation in GABAB receptor knockout mice.GABAB受体与葡萄糖稳态:对GABAB受体基因敲除小鼠的评估
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