Topological analysis of striatal lesions induced by 3-nitropropionic acid in the Lewis rat

被引:40
作者
Blum, D [1 ]
Gall, D [1 ]
Cuvelier, L [1 ]
Schiffmann, SN [1 ]
机构
[1] ULB Erasme, Dept Neurosci, Neurophysiol Lab, B-1070 Brussels, Belgium
关键词
Huntington's disease; Lewis rats; 3-nitropropionic acid; striatum; succinate dehydrogenase; topology;
D O I
10.1097/00001756-200106130-00050
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
3-Nitropropionic acid (3NP) is a succinate dehydrogenase inhibitor classically used to create animal models of Huntington's disease (HD). However, the effects of this neurotoxin are highly variable in the Sprague-Dawley rat strain, impeding the interest of such model in neuroprotection assays. In the present study, we found that continuous s.c. infusion of 3NP in the Lewis rat strain produces homogeneous clinical impairments as well as highly reproducible striatal lesions according to their location and size. More especially, using quantitative reconstructions, we have determined, after 5 days of treatment, that the lesion was topologically reproducible in the lateral part of the striatum in all tested rats. Thus, 3NP-treated Lewis rat provides an improved animal model for testing neuroprotective strategies in HD. NeuroReprt 12:1769-1772 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:1769 / 1772
页数:4
相关论文
共 18 条
  • [1] Metabolic compromise with systemic 3-nitropropionic acid produces striatal apoptosis in Sprague-Dawley rats but not in BALB/c ByJ mice
    Alexi, T
    Hughes, PE
    Knüsel, B
    Tobin, AJ
    [J]. EXPERIMENTAL NEUROLOGY, 1998, 153 (01) : 74 - 93
  • [2] 3-nitropropionic acid's lethal triplet: cooperative pathways of neurodegeneration
    Alexi, T
    Hughes, PE
    Faull, RLM
    Williams, CE
    [J]. NEUROREPORT, 1998, 9 (11) : R57 - R64
  • [3] BEAL MF, 1993, J NEUROSCI, V13, P4181
  • [4] Bezin L, 2000, SYNAPSE, V35, P201, DOI 10.1002/(SICI)1098-2396(20000301)35:3<201::AID-SYN5>3.0.CO
  • [5] 2-V
  • [6] Brouillet E, 1998, J NEUROCHEM, V70, P794
  • [7] Replicating Huntington's disease phenotype in experimental animals
    Brouillet, E
    Condé, F
    Beal, MF
    Hantraye, P
    [J]. PROGRESS IN NEUROBIOLOGY, 1999, 59 (05) : 427 - 468
  • [8] BASAL GANGLIA DEGENERATION, MYELIN ALTERATIONS, AND ENZYME-INHIBITION INDUCED IN MICE BY THE PLANT TOXIN 3-NITROPROPANOIC ACID
    GOULD, DH
    GUSTINE, DL
    [J]. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1982, 8 (05) : 377 - 393
  • [9] Quantifiable bradykinesia, gait abnormalities and Huntington's disease-like striatal lesions in rats chronically treated with 3-nitropropionic acid
    Guyot, MC
    Hantraye, P
    Dolan, R
    Palfi, SM
    Maziere, M
    Brouillet, E
    [J]. NEUROSCIENCE, 1997, 79 (01) : 45 - 56
  • [10] EARLY LOSS OF NEOSTRIATAL STRIOSOME NEURONS IN HUNTINGTONS-DISEASE
    HEDREEN, JC
    FOLSTEIN, SE
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (01) : 105 - 120