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Neuroadaptive changes in the mesocortical glutamatergic system during chronic nicotine self‐administration and after extinction in rats
Author(s) -
Wang Fan,
Chen Hao,
Sharp Burt M.
Publication year - 2008
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2008.05456.x
Subject(s) - nicotine , glutamatergic , nmda receptor , glutamate receptor , nbqx , ampa receptor , ventral tegmental area , neuroscience , self administration , pharmacology , chemistry , neurotransmission , dopamine , biology , biochemistry , receptor , dopaminergic
Nicotine self‐administration causes adaptation in the mesocorticolimbic glutamatergic system, including the up‐regulation of ionotropic glutamate receptor subunits. We therefore determined the effects of nicotine self‐administration and extinction on NMDA‐induced glutamate neurotransmission between the medial prefrontal cortex (mPFC) and ventral tegmental area (VTA). On day 19 of nicotine SA, both regions were microdialyzed for glutamate while mPFC was sequentially perfused with Kreb’s Ringer buffer (KRB), 200 μM NMDA, KRB, 500 μM NMDA, KRB, and 100 mM KCl. Basal glutamate levels were unaffected, but nicotine self‐administration significantly potentiated mPFC glutamate release to 200 μM NMDA, which was ineffective in controls. Furthermore, in VTA, nicotine self‐administration significantly amplified glutamate responses to both mPFC infusions of NMDA. This hyper‐responsive glutamate neurotransmission and enhanced glutamate subunit expression were reversed by extinction. Behavioral studies also showed that a microinjection of 2‐amino‐5‐phosphonopentanoic acid (NMDA‐R antagonist) into mPFC did not affect nicotine or sucrose self‐administration. However, in VTA, NBQX (AMPA‐R antagonist) attenuated both nicotine and sucrose self‐administration. Collectively, these studies indicate that mesocortical glutamate neurotransmission adapts to chronic nicotine self‐administration and VTA AMPA‐R may be involved in the maintenance of nicotine self‐administration.