Regional neuropathology following kainic acid intoxication in adult and aged C57BL/6J mice

被引:48
作者
Benkovic, SA [1 ]
O'Callaghan, JP [1 ]
Miller, DB [1 ]
机构
[1] Ctr Dis Control & Prevent, NIOSH, Toxicol & Mol Biol Branch, Morgantown, WV 26505 USA
关键词
age factor; excitotoxicity; gliosis; neuropathology;
D O I
10.1016/j.brainres.2005.11.065
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We evaluated regional neuropathological changes in adult and aged male mice treated systemically with kainic acid (KA) in a strain reported to be resistant to excitotoxic neuronal damage, C57BL/6. KA was administered in a single intraperitoneal injection. Adult animals were dosed with 35 mg/kg KA, while aged animals received a dose of 20 mg/kg in order to prevent excessive mortality. At time-points ranging from 12 h to 7 days post-treatment, animals were sacrificed and prepared for histological evaluation utilizing the cupric-silver neurodegeneration stain, immunohistochemistry for GFAP and IgG, and lectin staining. In animals of both ages, KA produced argyrophilia in neurons throughout cortex, hippocampus, thalamus, and amygdala. Semi-quantitative analysis of neuropathology revealed a similar magnitude of damage in animals of both ages, even though aged animals received less toxicant. Additional animals were evaluated for KA-induced reactive gliosis, assayed by an ELISA for GFAP, which revealed a 2-fold elevation in protein levels in adult mice, and a 2.5-fold elevation in aged animals. Histochemical evaluation of GFAP and lectin staining revealed activation of astrocytes and microglia in regions with corresponding argyrophilia. IgG immunostaining revealed a KA-induced breach of the blood-brain barrier in animals of both ages. Our data indicate widespread neurotoxicity following kainic acid treatment in C57BL/6J mice, and reveal increased sensitivity to this excitotoxicant in aged animals. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 231
页数:17
相关论文
共 65 条
[1]   Epileptogenesis and chronic seizures in a mouse model of temporal lobe epilepsy are associated with distinct EEG patterns and selective neurochemical alterations in the contralateral hippocampus [J].
Arabadzisz, D ;
Antal, K ;
Parpan, F ;
Emri, Z ;
Fritschy, JM .
EXPERIMENTAL NEUROLOGY, 2005, 194 (01) :76-90
[2]   Characterization of neuronal death induced by focally evoked limbic seizures in the C57BL/6 mouse [J].
Araki, T ;
Simon, RP ;
Taki, W ;
Lan, JQ ;
Henshall, DC .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 69 (05) :614-621
[3]   Kainate, a double agent that generates seizures: two decades of progress [J].
Ben-Ari, Y ;
Cossart, R .
TRENDS IN NEUROSCIENCES, 2000, 23 (11) :580-587
[4]   Sensitive indicators of injury reveal hippocampal damage in C57BL/6J mice treated with kainic acid in the absence of tonic-clonic seizures [J].
Benkovic, SA ;
O'Callaghan, JP ;
Miller, DB .
BRAIN RESEARCH, 2004, 1024 (1-2) :59-76
[5]  
BENKOVIC SA, 2000, SOC NEUR ANN M NEW O
[6]   Neuronal degeneration in rat forebrain resulting from D-amphetamine-induced convulsions is dependent on seizure severity and age [J].
Bowyer, JF ;
Peterson, SL ;
Rountree, RL ;
Tor-Agbidye, J ;
Wang, GJ .
BRAIN RESEARCH, 1998, 809 (01) :77-90
[7]   AGE-RELATED GLIOSIS IN THE WHITE MATTER OF MICE [J].
BRONSON, RT ;
LIPMAN, RD ;
HARRISON, DE .
BRAIN RESEARCH, 1993, 609 (1-2) :124-128
[8]   Endogenous brain-derived neurotrophic factor protects dopaminergic nigral neurons against transneuronal degeneration induced by striatal excitotoxic injury [J].
Canudas, AM ;
Pezzi, S ;
Canals, JM ;
Pallás, M ;
Alberich, J .
MOLECULAR BRAIN RESEARCH, 2005, 134 (01) :147-154
[9]   Reductions in spontaneous locomotor activity in aged male, but not female, rats in a model of early Parkinson's disease [J].
Cass, WA ;
Peters, LE ;
Smith, MP .
BRAIN RESEARCH, 2005, 1034 (1-2) :153-161
[10]   Joining particulate and whisker ceramic composites by plastic flow [J].
Chen, N ;
Gutierrez-Mora, F ;
Koritala, RE ;
Goretta, KC ;
Routbort, JL ;
Pan, JS .
COMPOSITE STRUCTURES, 2002, 57 (1-4) :135-139