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两种帕金森病大鼠糖脂代谢模型的比较 被引量:1

Comparison of glucose and lipid metabolism in two types of Parkinson's disease rat models
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摘要 目的筛选合并代谢异常的帕金森病模型,为后续的相关实验研究提供理想的动物模型。方法SD雄性大鼠62只,随机分为损毁前脑内侧束(MFB)模型组、损毁MFB假手术组、损毁纹状体模型组和损毁纹状体假手术组。模型制做成功后进行旋转实验,两组大鼠中分别选出成功模型,并分别对两组成功的PD模型大鼠的摄食、体重、血糖和腹腔内脂肪组织进行检测。观察两组模型大鼠上述代谢指标的变化。结果损毁MFB较损毁纹状体制作帕金森病模型的成功率高(70.97%比38.71%)。与各假手术组大鼠相比,MFB模型大鼠既出现体重明显的减轻[(218.1±13.99)g比(252.7±10.1)g,P<0.05],腹腔注射葡萄糖后15min和30min血糖出现了明显升高,并且肾周白色脂肪组织明显减少(左右两侧)。纹状体模型大鼠仅饮食减少[(13.95±0.25)g比(20.23±0.86)g,P<0.001]和腹腔注射葡萄糖后15min、30min和60min时间点血糖升高。结论损毁MFB的PD模型大鼠无论模型成功率还是代谢相关指标都较损毁纹状体的PD模型更接近糖脂代谢异常的PD患者。 Objective To select an ideal Parkinson ’ s disease ( PD) animal model with metabolic abnormalities for subsequent experimental studies .Methods A total of 62 Sprague-Dawley male rats were randomly divided into four groups:damaged medial forebrain bundle ( MFB) model group, damaged medial forebrain bundle ( MFB) sham group, damaged Striatum model group and damaged Striatum sham group .After detecting the rotation experiment , successful model rats of two groups were selected to detect the changes of food intake , body weight , blood glucose and intra-abdominal adipose tissue.Results It was easier to produce a PD model by destroying MFB than striatum .Compared with sham-operated rats, MFB model rats showed significant abnormality both in reduction of body weight [(218.1 ±13.99) g vs (252.7 ±10.1)g, P〈0.05] and high blood glucose appeared at 15min and 30min after introperitoneal glucose tolerance test ( IPGTT) .Their perirenal white adipose tissue was significantly reduced ( both left and right side ) .Striatum model rats only appeared decreased food intake [(13.95 ±0.25)g vs (20.23 ±0.86)g, P〈0.001] and impaired glucose regulation at 15min, 30min and 60min after IPGTT.Their body weight and adipose tissue did not change significantly .Conclusion No matter in the success rate or metabolism-related indicators , MFB damaged rat model of PD is more suitable to study PD patients with abnormal lipid metabolism compared with Striatum rat model .
出处 《解剖学报》 CAS CSCD 北大核心 2014年第5期605-609,共5页 Acta Anatomica Sinica
基金 国家自然科学基金资助项目(31171126)
关键词 帕金森病 糖脂代谢 6羟多巴胺 免疫组织化学 大鼠 Parkinson disease Glucose and lipid metabolism 6-hydroxydopamine Immunohistochemistry Rat
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  • 1Kashihara K. Weight loss in Parkinson's disease[J]. J Neurol, 2006,253 ( Sup pi 7) : V1I38-41.
  • 2U c EY, Struck LK, Rodnitzky RL, et al. Predictors of weight loss in Parkinson's disease[J]. Mov Disord,2006,21 (7) : 930-936.
  • 3Lorefalt B, Ganowiak W, Palhagen S, et al. Factors of importance for weight loss in elderly patients with Parkinson's disease [J] . Acta Neurol Scand, 2004, 110 (3) : 180-187.
  • 4Markus HS, Tomkins AM, Stern GM. Increased prevalence of undernutrition in Parkinson's disease and its relationship to clinical disease parameters [J]. J Neural Transm Park Dis Dement Sect, 1993,5(2): 117-125.
  • 5Barbeau A, Pourcher E. New data on the genetics of Parkinson's disease [J]. Can J Neurol Sci,1982, 9(1) : 53-60.
  • 6Sandyk R. The relationship between diabetes mellitus and Parkinson's disease[J]. Int J Neurosci ,1993,69 ( 1-4) : 125-130.
  • 7Wilhelm KR, Yanamandra K, Gruden MA, et al. Immune reactivity towards insulin, its amyloid and protein S100B in blood sera of Parkinson's disease patients [J]. Eur J Neurol, 2007 , 14 (3) : 327 -334.
  • 8Papapetropoulos S, Ellul J, Argyriou AA, et al. The effect of vascular disease on late onset Parkinson' s disease [J]. Eur J Neurol,2004, 11 (4) : 231-235.
  • 9Cannon JR, Greenamyre JT. Neurotoxic in vivo models of Parkinson's disease recent advances [J]. Prog Brain Res, 2010 , 184: 17-33.
  • 10Heikkila RE, Shapiro BS, Duvoisin RC. The relationship between loss of dopamine nerve terminals, striatal [3 H] spiroperidol binding and rotational behavior in unilaterally 6-hydroxydopamine-lesioned rats[J]. Brain Res ,1981, 211 (2) : 285-292.

二级参考文献17

  • 1曾宪智,孙晓红,高尔静,姬曼,蔡青,徐群渊.6-羟多巴胺单侧损伤大鼠黑质纹状通路后多巴胺受体的长时程变化[J].中国临床康复,2006,10(18):62-66. 被引量:3
  • 2Missale C,Nash R,Robinson SW,et al.Dopamine receptors:from structure to function[J].Physiol Rev,1998,78 (1):189-225.
  • 3Andres ME,Gysling K,Bustos G.Differential regulation of dopamine release by N-methyl-D-aspartate receptors in rat striatum after partial and extreme lesions of the nigro-striatal pathway[J].Brain Res,1998,797(2):255-266.
  • 4Dumartin B,Jaber M,Gonon F,et al.Dopamine tone regulates D1 receptor trafficking and delivery in striatal neurons in dopamine transporter-deficient mice[J].PNAS,2000,97(4):1879-1884.
  • 5Hersch SM,Ciliax BJ,Gutekunst CA,et al.Electron microscopic analysis of D1 and D2 dopamine receptor proteins in the dorsal striatum and their synaptic relationships with motor corticostriatal afferents[J].J Neurosci,1995,15(7 Pt 2):5222-5237.
  • 6Graybiel AM,Hirsch EC,Agic Y.The Nigrostriatal System in Parkinson's Disease.In:Streifler MB,Korczyn AD,Melamed E,Youdim MBH,eds.Advances in Neurology[M].Vol 53,Parkinson's Disease:Anatomy,Pathology and Therapy.New York:Ravern Press,1990:17-29.
  • 7Nusser Z,Mulvihill E,Streit P,et al.Subsynaptic segregation of metabotropic and ionotropic glutamate receptors as revealed by immunogold localization[J].Neurosci,1994,61(3):421-427.
  • 8Caille I,Dumartin B,Bloch B.Ultrastructural localization of D1 dopamine receptor immunoreactivity in rat striatonigral neurons and its relation with dopaminergic innervation[J].Brain Res,1996,730(1-2):11-17.
  • 9Xu ZC,Ling GY,Sahr RN,et al.Asymmetrical changes of dopamine receptors in the striatum after umilateral dopamine depletion[J].Brain Reseach,2005,1038(2):163-170.
  • 10Zigmond MJ,Abercronmbie ED,Berger TW,et al.Compensations after lesions of central dopaminergic neurons:some clinical and basic implications[J].TINS,1990,13(7):290-296.

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