In vivo role of Rho-kinase in glucose metabolism
In vivo role of Rho-kinase in glucose metabolism
批准号:
7138052
负责人:
YOUNG-BUM KIM
金额:
$20.2万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-07-01 至 2008-06-30
关键词:
adipocytesadipose tissuebiological signal transductionbody compositionenzyme activityenzyme mechanismgene expressiongenetically modified animalsglucose metabolismglucose transportglucose transporterguanine nucleotide binding proteininsulin sensitivity /resistancelaboratory mouserecombinaseserine threonine protein kinase
中文摘要
描述(由申请方提供):胰岛素急性刺激外周组织葡萄糖摄取和代谢的能力对正常葡萄糖稳态至关重要。对胰岛素这种作用的抵抗是2型糖尿病和肥胖症的主要致病特征。尽管已经确定了胰岛素信号传导中的许多近端步骤,但胰岛素维持葡萄糖稳态的分子机制仍不清楚。我们最近的研究表明,Rho激酶是胰岛素作用和葡萄糖稳态的重要介质。我们发现Rho激酶通过IRS-1丝氨酸磷酸化调节培养的脂肪细胞和肌肉细胞中胰岛素刺激的葡萄糖转运和信号,建立了一种新的葡萄糖转运和胰岛素信号调节机制。在本申请中,我们将进一步定义Rho激酶在体内葡萄糖转运和胰岛素敏感性调节中的生理作用,使用遗传方法。在目标1中,我们将开发转基因小鼠,其中Rho激酶的过表达是有条件地调节组织特异性Cre重组酶共表达。我们将通过与脂联素Cre重组酶转基因小鼠交配,获得脂肪特异性Rho激酶转基因小鼠。在目标2中,我们将研究Rho激酶在脂肪细胞中的选择性表达对全身胰岛素敏感性、葡萄糖稳态和体内瘦度的影响。这些研究将有助于更好地了解葡萄糖稳态调节机制,并可能为糖尿病和肥胖症的治疗提供新的靶点。胰岛素抵抗是2型糖尿病的主要危险因素,其原因尚不完全清楚。初步数据表明,Rho激酶功能的抑制导致胰岛素反应降低,导致胰岛素抵抗。本研究的目的是确定Rho激酶在葡萄糖稳态和胰岛素敏感性调节中的生理意义。这些实验可能会导致新的糖尿病药物的潜在目标的确定。
英文摘要
DESCRIPTION (provided by applicant): Insulin's ability to acutely stimulate glucose uptake and metabolism in peripheral tissues is essential for normal glucose homeostasis. Resistance to this effect of insulin is a major pathogenic feature of type 2 diabetes and obesity. Although many of the proximal steps in insulin signaling have been identified, the molecular mechanism(s) for insulin action to maintain glucose homeostasis are still unclear. Our recent study suggests that Rho-kinase is an important mediator of insulin action and glucose homeostasis. We found that Rho-kinase regulates insulin-stimulated glucose transport and signaling via IRS-1 serine phosphorylation in cultured adipocytes and muscle cells, establishing a novel mechanism for the regulation of glucose transport and insulin signaling. In this application, we will further define the physiological role of Rho-kinase in the regulation of glucose transport and insulin sensitivity in vivo, using genetic approaches. In Aim 1, we will develop transgenic mice in which Rho-kinase overexpression is conditionally regulated tissue specifically by Cre recombinase co-expression. We will generate adipose-specific Rho-kinase transgenic mice by breeding with the adiponectin Cre recombinase transgenic mice. In Aim 2, we will examine the effects of Rho-kinase expression selectively in adipocytes on whole-body insulin sensitivity, glucose homeostasis, and leanness in vivo. These studies will provide a better understanding of the mechanisms for regulation of glucose homeostasis, and may offer a novel target for the treatment of diabetes and obesity. Insulin resistance is a major risk factor for type 2 diabetes, and the cause of this is not fully understood. Preliminary data show that inhibition of Rho-kinase function results in a decreased insulin response, leading to insulin resistance. The goal of the study is to determine the physiological significance of Rho-kinase in the regulation of glucose homeostasis and insulin sensitivity. These experiments could lead to the identification of a potential target for new diabetes drugs.
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