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Regional neuropathology following kainic acid intoxication in adult and aged C57BL/6J mice
Authors:Benkovic Stanley Anthony  O'Callaghan James Patrick  Miller Diane Bemis
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.
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.
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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