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高脂饮食诱导肥胖模型大鼠骨骼肌组织蛋白酪氨酸磷酸酯酶1B和胰岛素受体底物2的表达
引用本文:赵 慧,于苏国,王令令,赵艳敏. 高脂饮食诱导肥胖模型大鼠骨骼肌组织蛋白酪氨酸磷酸酯酶1B和胰岛素受体底物2的表达[J]. 中国组织工程研究, 2012, 16(20): 3698-3702. DOI: 10.3969/j.issn.1673-8225.2012.20.020
作者姓名:赵 慧  于苏国  王令令  赵艳敏
作者单位:1滨州医学院附属医院内分泌科,山东省滨州市256603;2滨州市人民医院,山东省滨州市 256600
摘    要:背景:外周组织的胰岛素抵抗是2型糖尿病的主要病因。目的:观察高脂饮食诱导的肥胖大鼠骨骼肌中蛋白酪氨酸磷酸酯酶1B和胰岛素受体底物2的表达。方法:将20只SD大鼠随机等分为对照组和高脂组,分别给予常规饲料和高脂饲料喂养12周。结果和结论:与对照组相比,高脂组大鼠胰岛素敏感指数显著降低(P < 0.01),大鼠葡萄糖耐量受损,胰岛素释放试验提示葡萄糖刺激的胰岛素第一时相分泌受损,骨骼肌组织中蛋白酪氨酸磷酸酯酶1B蛋白表达水平明显增加(P < 0.01),骨骼肌中胰岛素诱导的胰岛素受体底物2磷酸化程度降低(P < 0.01)。提示高脂饮食诱导的肥胖大鼠骨骼肌中蛋白酪氨酸磷酸酯酶1B蛋白表达量升高,使胰岛素诱导的胰岛素受体底物2磷酸化程度降低,可能是肥胖导致胰岛素抵抗的机制之一。 关键词:肥胖;蛋白酪氨酸磷酸酶1B;胰岛素受体底物2;骨骼肌;胰岛素抵抗doi:10.3969/j.issn.1673-8225.2012.20.020

关 键 词:肥胖  蛋白酪氨酸磷酸酶1B  胰岛素受体底物2  骨骼肌  胰岛素抵抗  
收稿时间:2012-01-29

Expression of protein-tyrosine phosphatase 1B and insulin receptor substrate 2 in the skeletal muscle of rats with insulin resistance induced by high-fat diet
Zhao Hui,Yu Su-guo,Wang Ling-ling,Zhao Yan-min. Expression of protein-tyrosine phosphatase 1B and insulin receptor substrate 2 in the skeletal muscle of rats with insulin resistance induced by high-fat diet[J]. Chinese Journal of Tissue Engineering Research, 2012, 16(20): 3698-3702. DOI: 10.3969/j.issn.1673-8225.2012.20.020
Authors:Zhao Hui  Yu Su-guo  Wang Ling-ling  Zhao Yan-min
Affiliation:1Department of Endocrinology, Binzhou Medical University Hospital, Binzhou  256603, Shandong Province, China; 2Binzhou People’s Hospital, Binzhou  256600, Shandong Province, China
Abstract:BACKGROUND: Insulin resistance in the peripheral tissue is a major cause of type 2 diabetes mellitus. OBJECTIVE: To observe the expression of protein tyrosine phosphatase 1B (PTP-1B) and insulin receptor substrate 2 (IRS-2) in the skeletal muscle of rats with insulin resistance induced by high-fat diet. METHODS: Twenty SD rats were randomly divided into normal control group with 10 rats and high-fat diet group with 10 rats. Rats in the two groups were fed with normal diet and high-fat diet for 12 weeks, respectively.RESULTS AND CONCLUSION: The insulin sensitive index was significantly decreased in the high-fat diet rats compared with the normal rats (P < 0.01). In obese rats, glucose tolerance and the acute first-phase insulin secretory response to glucose were impaired. The protein level of PTP-1B in the skeletal muscle of obese rats was significantly increased compared with the control group (P < 0.01). Insulin-stimulated IRS-2 phosphorylation in the skeletal muscle was reduced in the obese rats (P < 0.01). These indicate that the increased PTP-1B level and the reduced insulin-stimulated IRS-2 phosphorylations in the skeletal muscle seem to play an important role in the insulin resistance induced by high-fat diet.
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