Regional neuropathology following kainic acid intoxication in adult and aged C57BL/6J mice |
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Authors: | Benkovic Stanley Anthony O'Callaghan James Patrick Miller Diane Bemis |
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Affiliation: | Toxicology and Molecular Biology Branch, Centers for Disease Control and Prevention-National Institute for Occupational, Safety and Health, Mailstop 3014, 1095 Willowdale Road, Morgantown, WV 26505, USA. |
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Abstract: | 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. |
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Keywords: | ABC, avidin-biotin complex ah, alveus hippocampi amyg, amygdala ANOVA, analysis of variance atc, area transitionalis corticoamygdaloidea BCA, bicinchoninic acid CA1, cornu ammonis region 1 CA3, cornu ammonis region 3 ccac, cortex cerebri, area cinguli CDC, Centers for Disease Control and Prevention cn, caudate nucleus DAB, 3-3′ diaminobenzidine tetrahydrochloride DPBS, Dulbecco's modified phosphate buffered saline ectx, entorhinal cortex EEG, electroencephalogram ELISA, enzyme-linked immunosorbent assay fctx, frontal cortex GFAP, glial fibrillary acidic protein hfd, hilus fasciae dentatae hip, hippocampus HRP, horseradish peroxidase i.e., id est IgG, immunoglobulin G III, cortex cerebri, layer III i.p., intraperitoneal IsoB4, Griffonia simplicifolia isolectin B4 KA, kainic acid lpeae, lamina principalis externa areae entorhinalis lpiae, lamina principalis interna areae entorhinalis nab, nucleus amygdaloideus basalis nac, nucleus amygdaloideus corticalis nah, nucleus anterior hypothalami nam, nucleus amygdaloideus medialis nat, nucleus anteroventralis thalami NIOSH, National Institute for Occupational Safety and Health nlh, nucleus lateralis hypothalami nls, nucleus lateralis septi nms, nucleus medialis septi npt, nucleus paratenialis thalami npvt, nucleus paraventricularis thalami nrt, nucleus reticularis thalami NSA, NeuroScience Associates nts, nucleus triangularis septi nvh, nucleus ventricularis hypothalami nvtpa, nucleus ventralis thalami, pars anterior nvtpd, nucleus ventralis thalami, pars dorsalis PBS, phosphate buffered saline ps, parasubiculum rcc, radiatio corporis callosi RT, room temperature scc, splenium corporis callosi SDS, sodium dodecyl sulfate SEM, standard error of the mean sl-m, stratum lacunosum-moleculare hippocampi smaid, stratum moleculare areae interna dentatae so, stratum oriens hippocampi sp, stratum pyramidale hippocampi sps, stratum pyramidale subiculi sr, stratum radiatum hippocampi tcc, truncus corporis callosi thal, thalamus VI, cortex cerebri, layer VI |
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