Immediate-early gene expression in the brain of the thiamine-deficient rat

Alan S. Hazell, Lynda McGahan, Wolfram Tetzlaff, Annie M. Bedard, George S. Robertson, Yusaku Nakabeppu, Antoine M. Hakim

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19 Citations (Scopus)

Résumé

Pyrithiamine-induced thiamine deficiency (PTD) in the rat is associated with neuronal loss in the thalamus and inferior colliculus. Recently, we were able to demonstrate the occurrence of apoptosis in the thalamus of these animals. Given that immediate-early genes (IEGs) participate in signal transduction pathways that mediate programmed cell death, the present study utilized in situ hybridization and immunohistochemistry to examine the expression of four IEGs (c-fos, c-jun, fos-B, and NGFI-A) during the progression of PTD. Elevated c-fos mRNA levels were initially observed in the posterior medial thalamus on d 12 of the deficiency. At the acute symptomatic stage (characterized by a loss of righting reflex on d 16-17), the posterior- medial thalamus exhibited increased mRNA for all genes examined, whereas the inferior colliculus demonstrated mRNA induction for c-fos, c-jun, and NGFI- A. Immunohistochemical analysis revealed that elevations of IEG mRNA associated with the acute symptomatic stage were consistently translated into protein in the thalamus. In contrast, whereas elevated Fos- and Jun-like immunoreactivity were detected in the inferior colliculus at this stage, NGFI-A-like immunoreactivity declined significantly below basal levels, suggesting a translational block. These results are consistent with our recent findings of apoptotic cell death, and indicate that differential patterns of IEG expression occur in the thalamus and inferior colliculus during PTD, which may contribute to the pathogenesis of this disorder.

Langue d'origineEnglish
Pages (de-à)1-15
Nombre de pages15
JournalJournal of Molecular Neuroscience
Volume10
Numéro de publication1
DOI
Statut de publicationPublished - 1998
Publié à l'externeOui

Note bibliographique

Funding Information:
The authors wish to thank Karen Chaundy for dedicated clerical assistance. This study was supported by a grant from the Medical Research Council of Canada.

ASJC Scopus Subject Areas

  • Cellular and Molecular Neuroscience

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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