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祛胰抵方对2型糖尿病大鼠肝脏IRS-2蛋白表达的影响

Effect on Quyidi Prescription on Liver IRS-2 Protein Expression of Type 2 Diabetes Mellitus
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摘要 目的 :观察2型糖尿病大鼠血糖、血清胰岛素浓度和胰岛素受体底物-2(insulin receptor substrate 2,IRS-2)的蛋白表达变化及祛胰抵方对其变化的影响。方法 :以小剂量链脲佐菌素(30 mg/kg)腹腔注射合并高脂饮食诱导2型糖尿病大鼠模型,给予不同剂量祛胰抵方治疗12周。分别测定其血糖、血清胰岛素浓度、肝脏组织的IRS-2蛋白表达。结果 :造模后2型糖尿病大鼠的血糖、血清胰岛素升高,肝脏组织的IRS-2蛋白表达下降;祛胰抵方能降低模型大鼠的血糖和血清胰岛素,并能显著升高肝脏组织IRS-2的蛋白表达。结论 :祛胰抵方治疗2型糖尿病可能与其提高肝脏组织IRS-2的蛋白表达从而改善胰岛素信号传导有关。 Objective : To investigate blood glucose, insulin and the protein expression of insulin receptor substrate-2 ( IRS-2 ) of type 2 diabetes mellitus ( T2DM ) rats and effects of Quyidi Prescription on these indexes. Methods : Model rats of T2DM were induced by intraperitoneal injectin of low dose streptozotocin( 30 mg/kg ) and fed on high fat-diet. Model rats were treated with different doses Quyidi Prescription for twelve weeks. After treatment, all rats were killed and following indexes were measured: blood glucose, insulin, expression of IRS- 2 protein in liver. Resuhs : After building model, the blood glucose, insulin of T2DM rats were increased, and expression of IRS-2 protein in liver was decreased in T2DM rats. Quyidi Prescription can reduce the blood glucose and insulin and increase the expression of IHS-2 protein in liver of T2DM rats. Conclusion : The mechanism of Quyidi Prescription treating T2DM may be partly by raising IRS-2 protein expression in liver to improve insulin resistance.
出处 《辽宁中医药大学学报》 CAS 2014年第3期7-9,共3页 Journal of Liaoning University of Traditional Chinese Medicine
基金 黑龙江省自然科学基金项目(D201072)
关键词 2型糖尿病 祛胰抵方 胰岛素受体底物-2 type 2 diabetes mellitus( T2DM ) Quyidi Prescription insulin receptor substrate-2( IRS-2)
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参考文献9

  • 1KidoY, Nakae J, Aeeili D.Clinieal reeview 125:The insulin reeeplor and its cellular largels[ J ] .J Clin Endoerinol Metab, 2001,86 ( 3 ) : 972-979.
  • 2Saad MU, Folli F, Kahn CR.lnsulin and dexamelhasone regulate insnlin reeeplors, insalin reeeptor substrate-l, and phosphatidylinositol3-kinase in Fao hepatoma cells [ J ] .Endoenr- inology, 1995,36 : 1579-1588.
  • 3Kubota N, Tnbe K, Teraoehi Y, et al.Disruption of insulin receptor substrate 2 cause type 2 diabetes because of liver insulin resisitance and lack of compensatory beta-cell hyperplasia [ J ]. Diabetes, 2000,49 : 1880-1889.
  • 4Kitamura T, Kahn CR, Aecili D.lnsulin reeeptor knockout miee [ J ] .Annn Rev Physiol,2003,65 : 313-332.
  • 5Eseribano O, Arrihas M, Valverde AM, et al. IRS-3 mediates insulin-induced glucose uplake in differentiated IRS-2 brown adipoeytes [ J ] .Mol Cell Endoerinol, 2007,268 : 1-9.
  • 6Domimic JW, Julio SG, Heather T, et al.Disruption of IRS-2 eanse type 2 diabeles in mice [ J ] .Nature, 1998,391 : 900-904.
  • 7彭定琼,郭晓蕙,陈宇,高妍.胰岛素受体底物2在2型糖尿病大鼠肌肉、脂肪、肝脏中的蛋白表达及其意义[J].中国预防医学杂志,2006,7(5):405-407. 被引量:9
  • 8郭莉阁,马建,刘春燕.祛胰抵胶囊对2型糖尿病胰岛素抵抗患者血清IL-6的影响[J].中国中医药科技,2011,18(6):514-515. 被引量:5
  • 9闫玲玲,马建.祛胰抵方对2型糖尿病IR的临床观察[J].中医药学报,2012,40(1):113-115. 被引量:5

二级参考文献23

  • 1李光伟,Step.,L.检测人群胰岛素敏感性的一项新指数[J].中华内科杂志,1993,32(10):656-660. 被引量:2126
  • 2刘萍,何岚.白细胞介素-6与胰岛素抵抗[J].医学综述,2006,12(4):227-229. 被引量:6
  • 3黄吉峰,李延,吴限.益气养阴活血法治疗2型糖尿病合并冠心病36例临床观察[J].中医药信息,2006,23(2):33-34. 被引量:5
  • 4包慧敏,王冬春,郭立中.中药对人肾小球系膜细胞作用的体外研究[J].中药药理与临床,2006,22(5):32-34. 被引量:6
  • 5中华人民共和国卫生部.中药新药治疗消渴病(糖尿病)的临床研究指导原则.1993:215.
  • 6国家中医药管理局.中华人民共和国中医药行业标准[s].南京:南京大学出版社,1994.132.
  • 7Napravnik, K. The Successful Landside Access Policies at Zurich Airport. Proceedings of the International AirRail Conference, Washington, DC. 2000.
  • 8Rondinone CM, Wang LM, Lonnroth P, et al.Insulin receptor substrate (IRS) 1 is reduced and IRS-2 is the main docking protein for phosphatidylinositol 3 - kinase in adipocytes from subjects non- insulin-dependent diabetes mellitus. Proc Natl Acad Sci USA, 1997, 94:4171 - 4175.
  • 9Kawano K, Hirashima T, Mori S, et al. Spontaneous long - term hyperglycemic rat with diabetic complications: Otsuka Long- Evans Tokushima Fatty ( OLETF ) strain. Diabetes, 1902, 41 : 1422 -1428.
  • 10Mario JA Saad, Frenco F, Jeffrey A, et al. Modulation of insubin receptor, insulin receptor substrate - 1, and phosphatidylinositol 3 - kinase in liver and muscle of dexamethasone- treated rats. J Clin Invest,1993, 92: 2065-2072.

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