期刊
NEUROSCIENCE LETTERS
卷 479, 期 3, 页码 277-281出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2010.05.079
关键词
Alcoholism; ENT1; Glutamate neurotransmission; CGP37849; Microdialysis; Ataxia; Caudate-putamen; Nucleus accumbens
资金
- Samuel Johnson Foundation for Genomics at Mayo Clinic
- National Institutes of Health (NIH) [R01 AA015164, R01 AA018779]
- Korea Research Foundation
Alcohol-sensitive type 1 equilibrative nucleotide transporter (ENT1) is known to regulate glutamate signaling in the striatum as well as ethanol intoxication. However, it was unclear whether altered extracellular glutamate levels in ENT1(-/-) mice contribute to ethanol-induced behavioral changes. Here we report that altered glutamate signaling in ENT1-/- mice is implicated in the ethanol-induced locomotion and ataxia by NMDA receptor antagonist, CGP37849. ENT1(-/-) mice appear less intoxicated following sequential treatment with CGP37849 and ethanol, compared to ENT1(+/+) littermates on the rotarod. These results indicate that inhibiting NMDA glutamate receptors is critical to regulate the response and susceptibility of alcohol related behaviors. Interestingly, a microdialysis experiment showed that the ventral striatum of ENT1(-/-) mice is less sensitive to the glutamate-reducing effect of the NMDA receptor antagonist compared to the dorsal striatum. Our findings suggest that differential glutamate neurotransmission in the striatum regulates ethanol intoxication. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
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