Differential expression of group I metabotropic glutamate receptors in rat spinal cord somatic and autonomic motoneurons:: Possible implications for the pathogenesis of amyotrophic lateral sclerosis

被引:35
作者
Anneser, JMH
Borasio, GD
Berthele, A
Zieglgänsberger, W
Tölle, TR
机构
[1] Univ Munich, Klinikum Grosshadern, Dept Neurol, D-81377 Munich, Germany
[2] Max Planck Inst Psychiat, D-80804 Munich, Germany
[3] Tech Univ Munich, Dept Neurol, D-81675 Munich, Germany
关键词
D O I
10.1006/nbdi.1999.0237
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of somatic, but not autonomic, motoneurons. The reason for this selective vulnerability is unknown. The pathogenesis of ALS is thought to involve glutamatergic excitotoxic mechanisms. While overactivation of ionotropic glutamate receptors may trigger excitotoxicity, we have previously shown that stimulation of group I metabotropic glutamate receptors (mGluRs) can exert neuroprotective effects on cultured motoneurons. Using in situ hybridization, we found a differential expression of group I mGluRs (mGluR1 and 5) in rat spinal cord. Autonomic motoneurons from the sacral parasympathetic Onuf's nucleus and thoracic sympathetic neurons, which are spared in ALS, express high levels of mGluR5, while somatic motoneurons do not. In addition, mGluR1 mRNA is found only in smaller somatic motoneurons, which seem to be less vulnerable in ALS. Thus, differential mGluR expression might provide a possible clue to the selective vulnerability of different motoneuronal subpopulations in ALS. (C) 1999 Academic Press.
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页码:140 / 147
页数:8
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