Abstract
Accumulating evidence suggests that orexin signaling is involved in reward and motivation circuit functions. However, the underlying mechanisms are not yet fully understood. Here, we show that orexin-A potentiates AMPAR-mediated synaptic transmission in the striatum, possibly by regulating the surface expression of AMPARs. Primary culture of striatal neurons revealed increased surface expression of AMPARs following orexin-A treatment. The increase in surface-expressed AMPARs induced by orexin-A treatment was dependent on both ERK activation and the presence of extracellular Ca2+. In the corticostriatal synapses of rat brain slices, orexin-A bath-application caused a delayed increase in the AMPAR/NMDAR EPSC ratio, suggesting that orexin-A sets in motion a series of events that lead to functional alterations in the striatal circuits. Our findings provide a potential link between the activation of orexin signaling in the striatum in response to addictive substances and neural adaptations in the reward circuitry that may mediate the long-lasting addiction-related behaviors.
Original language | English |
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Pages (from-to) | 409-413 |
Number of pages | 5 |
Journal | Biochemical and biophysical research communications |
Volume | 378 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2009 Jan 16 |
Bibliographical note
Funding Information:This work was supported by the Korea Science and Engineering Foundation (KOSEF) Grant funded by the Korean Government (MEST) (R01-2007-000-11034-0). We thank Yoon Hee Bae for technical assistance and helpful discussions.
Keywords
- AMPA receptor
- Drug addiction
- Orexin-A
- Synaptic plasticity
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology