Regional and subunit-specific downregulation of acid-sensing ion channels in the pilocarpine model of epilepsy

被引:72
作者
Biagini, G
Babinski, K
Avoli, M
Marcinkiewicz, M
Séguéla, P
机构
[1] McGill Univ, Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[3] Univ Montreal, Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada
[4] Univ Modena & Reggio Emila, Dept Biomed Sci, Physiol Sect, I-41100 Modena, Italy
[5] Antalium Inc, Montreal, PQ H3A 1X6, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1006/nbdi.2000.0331
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acid-sensing ion channels (ASICs) constitute a recently discovered family of excitatory cation channels, structurally related to the superfamily of degenerin/epithelial sodium channels. ASIC1b and ASIC3 are highly expressed in primary sensory neurons and are thought to play a role in pain transmission related to acidosis. ASIC1a, ASIC2a, and ASIC2b are also distributed in the central nervous system where their function remains unclear. We investigated here the regulation of their expression during status epilepticus (SE), a condition in which neuronal overexcitation leads to acidosis. In animals treated with pilocarpine (380 mg/kg) to induce SE, we observed a marked decrease of ASlC2b mRNA levels in all hippocampal areas and of ASIC1a mRNA levels in the CA1-2 fields. These changes were also observed after protective treatment from neuronal cell death with diazepam (10 mg/kg) and pentobarbital (30 mg/kg). These findings suggest a key role of channels containing ASIC1a and ASIC2b subunits in both normal and pathological activity of hippocampus. (C) 2001 Academic Press.
引用
收藏
页码:45 / 58
页数:14
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