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猪糖尿病模型的制作及评价

Establishment and evaluation of experimental diabetic models in pigs
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摘要 目的:探索一种较好的类似于人类糖尿病的模型的方法。方法:选用贵州小香猪,联合应用链脲菌素、四氧嘧啶造模,连续监测血糖浓度;ELISA方法检测造模前后血清胰岛素水平。胰腺HE切片用来评价胰岛状态。结果:造模前,糖尿病模型组和正常对照组的体重、血糖和胰岛素水平均无显著性差异。造模后,与对照组相比,模型组体重显著下降(4.09±0.31 vs.6.42±0.56 kg,P<0.05),血糖显著升高(17.30±1.20 vs.4.30±0.32 mmol/L,P<0.05),胰岛素水平显著下降(0.04±0.02 vs.0.11±0.03μg/L,P<0.05)。HE切片显示模型组胰岛明显萎缩。结论:给小型猪静脉注射60 mg/kg链脲菌素和30 mg/kg四氧嘧啶可成功建立糖尿病模型,该剂量可作为复制猪糖尿病模型的参考标准。 Objective: To explore a better type 1 diabetes models similar to that of humans. Methods: Male Chinese laboratory miniature pigs administrated with streptozotocin and alloxan were used as subjects. The dynamic changes of the glucose contents in plasma were continuously measured and insulin was measured by ELISA. HE stained slides were used to value the islets state. Results:There were no significant difference in weight, glucose level and insulin level between diabetic group and controls before being models. Compared with normal controls: weight of models decreased (4. 09 ±0. 31 vs. 6. 42 ±0. 56 kg, P 〈0. 05) ; the glucose contents increased significantly( 17. 30 ± 1.20 vs. 4. 30 ± 0. 32 mmol/L ,P 〈 0. 05 )and insulin contents reduced (0. 04 ± 0. 02 vs. 0. 11 ±0. 03 ug/L, P 〈 0. 05 )in plasma. HE stained slides showed atrophic islets in diabetic models. Conclusion: The porcine type 1 diabetes mellitus models has been established successfully by injection of Streptozotocin (60 mg/kg) and Alloxan (30 mg/kg). The dose in this study could be eonsidered as a reference standard for porcine diabetic models.
出处 《中国卫生检验杂志》 CAS 2009年第7期1484-1486,共3页 Chinese Journal of Health Laboratory Technology
基金 河南省教育厅自然基金资助(2007310014)
关键词 糖尿病 模型 小型猪 Diabetes Models Miniature pigs
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  • 1于德民,吴锐,尹潍,袁咏.实验性链脲佐菌素糖尿病动物模型的研究[J].中国糖尿病杂志,1995,3(2):105-109. 被引量:425
  • 21996~2000年国家糖尿病防治规划纲要[J].中国慢性病预防与控制,1996,4(2):49-50. 被引量:80
  • 3Winzell MS, Ahren B. The high-fat diet-fed mouse: a model for studying mechanisms and treatment of impaired glucose tolerance and type 2 diabetes[J]. Diabetes,2004,53:S215 - 219.
  • 4Huang BW,Chiang MT, Yao HT, et al. The effect of high-fat and high-fructose diets on glucose tolerance and plasma lipid and leptin levels in rats[J]. Diabetes Obes Metab,2004,6: 120- 126.
  • 5Danda RS, Habiba NM, Rineon-Choles H, et al. Kidney involvement in a nongenetic rat model of type 2 diabetes[ J ]. Kidney Int, 2005,68 (6) : 2562 - 2571.
  • 6Zhang F,Ye C,Li G,et al. The rat model of type 2 diabetic mellitus and its glycometabolism characters[J]. Exp Anim,2003,52(5) : 401 - 407.
  • 7Rees DA, Alcolado JC. Animal models of diabetes mellitus [ J ]. Diabetic Medicine,2005,22(4) : 359 - 375.
  • 8Kadowaki T. Insights into insulin resistance and type 2 diabetes from knockout mouse models[J]. J Clin Inves,2000,106(4): 459- 465.
  • 9Leiter EH. Mice with targeted gene disruptions or gene insertions for diabetes research: problems, pitfalls, and potential solutions [ J ]. Diabetologia,2002,45:296 - 308.
  • 10Plum L,Wunderlich F T, Baudler S, et al. Transgenic and knockout mice in diabetes research: Novel insights into pathophysiology, limitations, and perspectives [ J ]. Physiology, 2005,20 ( 3 ) : 152 - 161.

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