Abstract
Recent studies have provided compelling evidence demonstrating that orexin (also known as hypocretin) neurons play a central role in the pathophysiology of narcolepsy. However, targeted deletion of orexin does not fully mimic the functional deficits induced by selective ablation of these neurons; implying that other secreted signaling molecules expressed in these neurons mediate key aspects of their function. In this study, we demonstrate that orexin neurons display robust expression of neuronal activity-regulated pentraxin (Narp), a secreted neuronal pentraxin, implicated in regulating clustering of α-amino-3-hydroxy-5-methylisoxazole 4-propionate (AMPA) receptors. Furthermore, we have found that hypothalamic melanin-concentrating hormone (MCH) neurons, which form a peptidergic pathway thought to oppose the effects of the orexin system, express another neuronal pentraxin, NP1. Thus, these findings suggest that these pathways utilize neuronal pentraxins, in addition to neuropeptides, as synaptic signaling molecules.
Original language | English (US) |
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Pages (from-to) | 1561-1565 |
Number of pages | 5 |
Journal | Journal of Neurochemistry |
Volume | 82 |
Issue number | 6 |
DOIs | |
State | Published - Sep 2002 |
Keywords
- AMPA receptors
- Immediate early gene
- Melanin-concentrating hormone (MCH)
- NP1
- Neuronal activity-regulated pentraxin (Narp)
- Orexin
ASJC Scopus subject areas
- Biochemistry
- Cellular and Molecular Neuroscience