3.8 Article

Low-voltage-activated calcium channel subunit expression in a genetic model of absence epilepsy in the rat

Journal

MOLECULAR BRAIN RESEARCH
Volume 75, Issue 1, Pages 159-165

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0169-328X(99)00307-1

Keywords

calcium channel; absence epilepsy; thalamus; in situ hybridization

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Funding

  1. NIMH NIH HHS [MH12091] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS033583, NS33583] Funding Source: Medline

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The Genetic Absence Epilepsy Rats from Strasbourg (GAERS) are an inbred strain of rats that display many of the characteristics of human absence epilepsy. In these rats, reciprocal thalamocortical projections play a critical role in the generation of spike-and-wave discharges that characterize absence seizures. When compared to those of the non-epileptic control strain, juvenile animals of the GAERS strain reportedly possess higher-amplitude T-type calcium currents in neurons of the thalamic reticular nucleus (nRt). We hypothesized that differences in calcium currents seen between GAERS and controls result from differences in expression of genes for low-voltage-activated calcium channels. Quantitative in situ hybridization was used to compare expression of alpha 1G, alpha 1H, alpha 1I, and alpha 1E calcium channel subunit mRNAs from adult and juvenile animals of the two strains. We found higher levels of alpha 1H mRNA expression in nRt neurons of juvenile animals (34.9 +/- 2.3 vs. 28.4 +/- 1.8 grains/10(3) pixels, p < 0.05), perhaps accounting in part for earlier reports of elevated T-type current amplitude in those cells. In adult GAERS animals, we found elevated levels of alpha 1G mRNA in neurons of the ventral posterior thalamic relay nuclei (64.8 +/- 3.5 vs. 53.5 +/- 1.7 grains/10(3) pixels, p < 0.05), as well as higher levels of alpha 1H mRNA in nRt neurons (32.6 +/- 0.8 vs. 28.2 +/- 1.6 grains/10(3) pixels, p < 0.05). These results suggest that the epileptic phenotype apparent in adult GAERS may result in part from these significant, albeit small (similar to 15-25%), elevations in T-type calcium channel mRNA levels. (C) 2000 Elsevier Science B.V. All rights reserved.

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