Targeting glutamate homeostasis for potential treatment of nicotine dependence

被引:18
作者
Alasmari, Fawaz [1 ]
Al-Rejaie, Salim S. [2 ]
AlSharari, Shakir D. [2 ,3 ]
Sari, Youssef [1 ]
机构
[1] Univ Toledo, Coll Pharm & Pharmaceut Sci, Dept Pharmacol & Expt Therapeut, Hlth Sci Campus,3000 Arlington Ave,HEB282G, Toledo, OH 43606 USA
[2] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia
[3] Virginia Commonwealth Univ, Med Coll Virginia, Dept Pharmacol & Toxicol, Richmond, VA 23298 USA
关键词
Nicotine; nAChRs; GLT-1; xCT; iGLURs; mGluRs; VENTRAL TEGMENTAL AREA; ALCOHOL-PREFERRING RATS; ANTAGONIST 6-METHYL-2-(PHENYLETHYNYL)-PYRIDINE MPEP; SELF-ADMINISTRATION BEHAVIOR; ETHANOL-DRINKING BEHAVIOR; INDUCED DOPAMINE RELEASE; BRAIN REWARD FUNCTION; D-ASPARTATE RECEPTORS; NUCLEUS-ACCUMBENS; PREFRONTAL CORTEX;
D O I
10.1016/j.brainresbull.2015.11.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several studies demonstrated that impairment in glutamatergic neurotransmission is linked to drug dependence and drug-seeking behavior. Increased extracellular glutamate concentration in mesocorticolimbic regions has been observed in animals developing nicotine dependence. Changes in glutamate release might be associated with stimulatory effect of nicotinic acetylcholine receptors (nAChRs) via nicotine exposure. We and others have shown increased extracellular glutamate concentration, which was associated with down regulation of the major glutamate transporter, glutamate transporter 1 (GLT-1), in brain reward regions of animals exposed to drug abuse, including nicotine and ethanol. Importantly, studies from our laboratory and others showed that upregulation of GLT-1 expression in the mesocorticolimbic brain regions may have potential therapeutic effects in drug dependence. In this review article, we discussed the effect of antagonizing presynaptic nAChRs in glutamate release, the upregulatory effect in GLT-1 expression and the role of glutamate receptors antagonists in the treatment of nicotine dependence. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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