3-硝基丙酸建模探讨亨廷顿舞蹈病发病机制进展
被引量:2
摘要
亨廷顿舞蹈病是由于亨廷顿基因中CAG序列异常扩增从而产生异常的亨廷顿蛋白,导致纹状体及大脑皮层的选择性神经变性,产生相应症状,目前发病机制尚不明确。能量代谢抑制剂3-硝基丙酸处理的大鼠模型可表现出与此病相似的病理特征及一部分临床症状,建模研究纹状体选择性变性的发病机制,涉及钙蛋白酶、半胱氨酸依赖的蛋白酶(Caspase)家族、氧自由基等细胞内途径,谷氨酸、多巴胺等细胞外途径。
出处
《国际神经病学神经外科学杂志》
2007年第4期335-339,共5页
Journal of International Neurology and Neurosurgery
参考文献25
-
1Li S, Li XJ. Multiple pathways contribute to the pathogenesis of Huntington disease. Mol Neurodegener, 2006, 1 : 19.
-
2The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell, 1993, 72(6) : 971-983.
-
3Powers WJ,Videen TO,Markham J,et al.Selective defect of in vivo glycolysis in early Huntington's disease striatum.Proc Natl Acad Sci U S A,2007,104(8):2945-2949.
-
4Gu X,Andre VM,Cepeda C,et al.Pathological cell-cell interactions are necessary for striatal pathogenesis in a conditional mouse model of Huntington's disease.Mol Neurodegener,2007,2:8.
-
5Brouillet E,Conde F,Beal MF,et al.Replicating Huntington's disease in experimental animals.Prog Neurobiol,1999,59(5):427-468.
-
6Ludolph AC,He F,Spencer PS,et al.3-Nitroproprionic acid-exogenous animal neurotoxin and possible human striatal toxin.Can J Neurol Sci,1991,18:492-498.
-
7Lee WT,Chang C.Magnetic resonance imaging and spectroscopy in assessing 3-nitropropionic acid-induced brain lesions:an animal model of Huntington's disease.Prog Neurobiol,2004,72(2):87-110.
-
8Brouillet E,Jacquard C,Bizat N,et al.3-Nitropropionic acid:a mitochondrial toxin to uncover physiopathological mechanisms underlying striatal degeneration in Huntington's disease.J Neurochem,2005,95(6):1521-1540.
-
9Beal MF,Brouillet E,Jenkins B,et al.Neurochemical and histological characterization of the striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid.J Neurosci,1993,13(10):1481-1492.
-
10Yamashima T.Implication of cysteine proteases calpain,cathepsin and caspase in ischemic neuronal death ofprimates.Prog Neurobiol,2000,62(3):273 -295.
同被引文献19
-
1吴素娟,刘道杰.衍生化HPLC法测定药物有效成分的研究进展[J].聊城大学学报(自然科学版),2005,18(4):45-48. 被引量:6
-
2冯埃生,邹汉法,汪海林,李瑞江,王学政,张玉奎.影响高效液相色谱/挥发激光散射检测器检测性能基本因素的考察[J].药物分析杂志,1996,16(6):414-417. 被引量:102
-
3Oskar H, Asa P, Marcel L, et al. Transgenic mice expressing a Huntington's disease mutation are resistant to quinolinic acid-induced striatal excitotoxicity[J]. Proc Natl Acad Sci U S A, 1999,96:8727 - 8732.
-
4Shilpa R, Jodi LM, Jeffrey HK. Animal models of Huntington's disease[J]. ILAR J,2007,48(4) :356 - 373.
-
5Emmanuel B, Carine J, Nicolas B, et al. 3-Nitropropionic acid: a mitoehondrial toxin to uncover physiopathological mechanisms underlying striatal degeneration in Huntington's disease[J]. J Neurochem,2005,95 : 1521 - 1540.
-
6Beal M F, Emmanuel B, Bruce G, et al. Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid [ J ]. The J Neurosci, 1993, 13(10) :4181 - 4192.
-
7Naoyuki N, Tom I. Fetal tissue transplants in animal models of Huntington's disease : the effects on damaged neuronal circuitry and behavioral deficits[J]. Progr Neurobiol,2000,61:313 - 338.
-
8Cesario VB, Theodore KK, Paul RS. 3-Nitropropionic acid animal model and Huntington's disease[J]. Neurosci Biohehav Rev, 1997,21 (3) :289 - 293.
-
9Bossi SR, Simpson JR, Isacson O. Age dependence of striatal neuronal death caused by mitochondrial dysfunction[J]. Neuroreport, 1993,4:73 - 76.
-
10Isabel L,Filomena F, Maribel C, et al. Changes in endocarmabinoid transmission in the basal ganglia in a rat model of Huntington's disease[J].Neuroreport,2001,12(10) :2125 - 2129.
引证文献2
-
1徐桂丽,朱天全,宋霜,李建其,周爱南,张庆伟.丁苯那嗪关键中间体及异构体杂质的测定研究[J].中国药物化学杂志,2020,30(11):669-674.
-
2王丹丹,李峰.三硝基丙酸动物模型和亨廷顿氏病[J].中国比较医学杂志,2009,19(8):70-75. 被引量:2
-
1宋海洋,金澎.Caspase家族与颞叶癫痫神经元凋亡[J].中华神经外科疾病研究杂志,2012,11(2):187-189. 被引量:3
-
2宋英,魏尔清,陈忠.Caspase与神经系统疾病[J].细胞生物学杂志,2004,26(3):227-230. 被引量:6
-
3静雨.与亨廷顿舞蹈病治疗有关的关键蛋白[J].国外医学情报,2002,23(12):18-18.
-
4张玉花,蔡蕊,刘江华,朱春雨,解洪荣.MPTP/MPP+诱导神经元凋亡的机制研究[J].现代生物医学进展,2011,11(5):964-967. 被引量:8
-
5李军.脑缺血性程序性细胞死亡的分子机制[J].国外医学(麻醉学与复苏分册),2002,23(1):12-16.
-
6王珂,谢文煌,王新强.促红细胞生成素对癫痫大鼠神经元的保护作用[J].中国神经免疫学和神经病学杂志,2007,14(4):235-235.
-
7睡眠障碍可能是痴呆的早期信号[J].保健医苑,2013(8):62-62.
-
8Jean-MarcBurgunder,冯璐扬.亨廷顿舞蹈病:教学性综述[J].中国神经精神疾病杂志,2015,41(10):577-591. 被引量:16
-
9ElenaCattaneo,王伟,等.亨廷顿氏病之谜[J].科学(中文版),2003(2):47-51.
-
10吉四辈,刘艳霞,马铭心.初诊为脑血管病的慢性硬膜下血肿52例临床分析[J].中国煤炭工业医学杂志,2003,6(8):702-703.