3-Nitropropionic acid animal model and Huntington' s disease

Neuroscience & Biobehavioral Reviews - Tập 21 - Trang 289-293 - 1997
Cesario V. Borlongan1, Theodore K. Koutouzis1, Paul R. Sanberg1
1Division of Neurological Surgery, Departments of Surgery, Neurology, Psychiatry, and Pharmacology, University of South Florida College of Medicine, MDC Box 16, 12901 Bruce B. Downs Blvd., Tampa, FL 33612 USA

Tài liệu tham khảo

Albin, 1992, Alternative excitotoxic hypothesis, Neurol., 42, 733, 10.1212/WNL.42.4.733 Ankarcrona, 1995, Glutamate induced neuronal death: a succession of necrosis or apoptosis depending on mitochondrial function, Neuron., 15, 961, 10.1016/0896-6273(95)90186-8 Beal, 1992, Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?, Ann. Neurol., 31, 119, 10.1002/ana.410310202 Beal, 1993, Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid, J. Neurosci., 13, 4181, 10.1523/JNEUROSCI.13-10-04181.1993 Borlongan, 1995, Systemic 3-nitropropionic acid: behavioral deficits and striatal damage in rats, Brain Res. Bull., 36, 549, 10.1016/0361-9230(94)00242-S Borlongan, 1995, Behavioral pathology induced by repeated systemic injections of 3-nitropropionic acid mimics the motoric symptoms of Huntington's disease, Brain Res., 697, 254, 10.1016/0006-8993(95)00901-2 Bossi, 1993, Age dependence of striatal neuronal death caused by mitochondrial dysfunction, Neuroreport., 4, 73, 10.1097/00001756-199301000-00019 Brouillet, 1993, Soc. Neurosci. Abstr., 19, 409 Brouillet, 1993, Age-dependent vulnerability of the striatum to the mitochondrial toxin 3-nitropropionic acid, J. Neurochem., 60, 356, 10.1111/j.1471-4159.1993.tb05859.x Brouillet, 1994, Systemic or local administration of azide produces striatal lesions by a energy impairment-induced excitotoxic mechanism, Exp. Neural., 129, 175, 10.1006/exnr.1994.1159 Bruyn, 1968, Huntington's chorea, historical, clinical and laboratory synopsis, Handbook Clin. Neurol., 6, 298 Cox, 1989, Excitatory amino acid neurotoxicity at the N-methyl-d-aspartate receptor in cultured neurons: role of the voltage-dependent magnesium block, Brain Res., 499, 267, 10.1016/0006-8993(89)90774-9 Filloux, 1990, Nigral dopamine type-1 are reduced in Huntington's disease: a postmortem autoradiographic study using the [3H] SCH23390 and correlation with [3H] forskolin binding, Exp. Neurol., 110, 219, 10.1016/0014-4886(90)90033-O Gould, 1982, Basal ganglia degeneration, myelin alterations, and enzyme inhibition in mice induced by the plant toxin 3nitropropionic acid, Neuropathol. Appl. Neurobiol., 8, 377, 10.1111/j.1365-2990.1982.tb00306.x Gusella, 1983, A polymorphic marker genetically linked to Huntington's disease, Nature, 306, 234, 10.1038/306234a0 Hamilton, 1987, Nature and distribution of brain lesions in rats intoxicated with 3-nitropropionic acid: a type of hypoxic (energy deficient) brain damage, Acta Neuropathol., 72, 286, 10.1007/BF00691103 Hantraye, 1990, A primate model of Huntington's disease: behavioural and anatomical studies of unilateral excitotoxic lesions of the caudate-putaman in the baboon, Exp. Neurol., 108, 91, 10.1016/0014-4886(90)90014-J Isacson, 1985, Neural grafting in the rat model of Huntington's disease: progressive neuro-chemical changes after neostriatal ibotenate lesions and tissue grafting, Neurosci., 16, 799, 10.1016/0306-4522(85)90095-8 Koroshetz, 1992, Localized proton—NMR spectroscopy in patients with Huntinton's disease (HD) demonstrates abnormal lactate levels in occipital cortex: evidence for compromised metabolism in HD, Neurology, 42, 319 Koutouzis, 1994, Intrastriatal. 3-nitropropionic acid: a behavioral assessment, Neuroreport., 5, 2241, 10.1097/00001756-199411000-00009 Koutouzis, 1994, Systemic 3-nitropropionic acid: long effects on locomotor behavior, Brain Res. Rev., 64, 242, 10.1016/0006-8993(94)90085-X Koutouzis, 1994, Cell transplantation for central nervous system disorders, CRC Crit. Rev. Neurobiol., 3, 25 Ludolph, 1991, 3-Nitropropionic acid-exogenous animal neurotoxin and possible human striatal toxin, Can. J. Neurol. Sci., 18, 492, 10.1017/S0317167100032212 Martin, 1986, Huntington's disease: pathenogenesis and management, N. Engl. J. Med., 315, 1267, 10.1056/NEJM198611133152006 Mettler, 1972, Choreoathetosis and striopallidonigral necrosis due to sodium azide, Exp. Neurol., 34, 291, 10.1016/0014-4886(72)90175-6 Nishino, 1995, Chronically administered 3-nitropropionic acid induces striatal lesions attributed to dysfunction of the blood-brain barrier, Neurosci. Lett., 186, 161, 10.1016/0304-3940(95)11311-J Novelli, 1988, Glutamate becomes neurorotoxic via the N-methyl-d-aspartate receptor when intracellular energies are reduced, Brain Res., 451, 205, 10.1016/0006-8993(88)90765-2 Sanberg, 1984, Scientific approaches to Huntington's disease, CRC Crit. Rev. Clin. Neurobiol., 1, 1 Shimano, 1995, Chronically administered 3-nitropropionic acid produces selective lesions in the striatum and reduces muscle toms, Obesity Res., 3, 779, 10.1002/j.1550-8528.1995.tb00499.x Shoulson, 1986, Huntington's Disease, 1258 Stober, 1984, Bicaudate diameter — the most specific and simplified CT parameter in the diagnosis of Huntington's disease, Neuroradiol., 26, 25, 10.1007/BF00328198 1993, A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes, Cell., 72, 971, 10.1016/0092-8674(93)90585-E Zorumski, 1993, Excitotoxic neuronal damage and neuropsychiatric disorders, J. Pharm. Ther., 59, 145, 10.1016/0163-7258(93)90043-D