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Exposure to nicotine and sensitization of nicotine-induced behaviors

机译:暴露于尼古丁并引起尼古丁诱发的行为

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摘要

Evidence for an important link between sensitization of midbrain dopamine (DA) neuron reactivity and enhanced self-administration of amphetamine and cocaine has been reported. To the extent that exposure to nicotine also sensitizes nucleus accumbens DA reactivity, it is likely that it will also impact subsequent drug taking. It is thus necessary to gain an understanding of the long-term effects of exposure to nicotine on nicotinic acetylcholine receptors (nAChRs), neuronal excitability and behavior. A review of the literature is presented in which different regimens of nicotine exposure are assessed for their effects on upregulation of nAChRs, induction of LTP in interconnected midbrain nuclei and development of long-lasting locomotor and DA sensitization. Exposure to nicotine upregulates nAChRs and nAChR currents and produces LTP of excitatory inputs to midbrain DA neurons. These effects appear in the hours to days following exposure. Exposure to nicotine also leads to long-lasting sensitization of nicotine’s nucleus accumbens DA and locomotor activating effects. These effects appear days to weeks after drug exposure. A model is proposed in which nicotine exposure regimens that produce transient nAChR upregulation and LTP consequently produce long-lasting sensitization of midbrain DA neuron reactivity and nicotine-induced behaviors. These neuroadaptations are proposed to constitute critical components of the mechanisms underlying the initiation, maintenance and escalation of drug use.
机译:已有证据表明中脑多巴胺(DA)神经元反应性致敏与安非他明和可卡因的自我给药增强之间存在重要联系。在一定程度上暴露于尼古丁也会使伏隔核DA反应性增敏,这很可能也会影响随后的药物服用。因此,有必要了解暴露于烟碱对烟碱乙酰胆碱受体(nAChRs),神经元兴奋性和行为的长期影响。提出了一篇文献综述,其中评估了不同的烟碱暴露方案对nAChRs上调,互连中脑核中LTP的诱导以及持久运动和DA致敏作用的影响。暴露于尼古丁会上调nAChR和nAChR电流,并产生中脑DA神经元兴奋性输入的LTP。这些影响会在暴露后数小时到数天出现。暴露于尼古丁也会导致尼古丁伏隔核DA的持久敏感性和运动激活作用。这些影响在药物暴露后数天至数周出现。提出了一个模型,其中产生瞬时nAChR上调和LTP的尼古丁暴露方案会中脑DA神经元反应性和尼古丁诱导的行为产生持久的致敏作用。提出这些神经适应性构成药物使用的起始,维持和升级基础机制的关键组成部分。

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