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Repeated morphine exposure decreased the nucleus accumbens excitability during short‐term withdrawal
Author(s) -
Heng LiJun,
Yang Jing,
Liu YiHui,
Wang WenTing,
Hu SanJue,
Gao GuoDong
Publication year - 2008
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.20551
Subject(s) - nucleus accumbens , morphine , neuroscience , depolarization , chemistry , medium spiny neuron , membrane potential , pharmacology , dopamine , medicine , psychology , striatum
It is well known that the nucleus accumbens plays an important role in drug reinforcing effect and relapse. However, the cellular neuroadaptations that take place in accumbens neurons after repeated drug exposure are still not well understood, especially for opioids. Here, we examined how nucleus accumbens neuronal excitability becomes affected in rats exposed to morphine using whole‐cell patch‐clamp recordings. Medium spiny neurons recorded from brain slices of repeated morphine treated rats exhibited a significant decrease in the intrinsic excitability after 3–4 days withdrawal, compared to that of neurons from saline treated animals, which was indicated by the increase of current to evoke the first spike and the decrease of spike number induced by depolarizing current steps in the morphine group. Moreover, the excitability decrease was accompanied by related membrane property changes, such as resting membrane potential hyperpolarization, input resistance, and membrane time constant decrease, inward rectification increase, and action potential duration decrease. Taken together, repeated morphine exposure and short‐term withdrawal may reduce nucleus accumbens activity and output by modulating intrinsic membrane properties of its output neurons, which could be an important neuroadaptation process that mediates morphine addictive effect. Synapse 62:775–782, 2008. © 2008 Wiley‐Liss, Inc.

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