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烟雾提取物和尼古丁而非烟草提取物增强小鼠腹侧被盖区多巴胺能神经元的放电和爆发活动。

Smoke extracts and nicotine, but not tobacco extracts, potentiate firing and burst activity of ventral tegmental area dopaminergic neurons in mice.

机构信息

Neurobiologie des Processus Adaptatifs, CNRS UMR 7102, University P. et M. Curie, Paris, France.

出版信息

Neuropsychopharmacology. 2011 Oct;36(11):2244-57. doi: 10.1038/npp.2011.112. Epub 2011 Jun 29.

Abstract

Nicotine prominently mediates the behavioral effects of tobacco consumption, either through smoking or when taking tobacco by snuff or chew. However, many studies question the exclusive role of nicotine in these effects. The use of preparations containing all the components of tobacco, such as tobacco and smoke extracts, may be more suitable than nicotine alone to investigate the behavioral effects of smoking and tobacco intake. In the present study, the electrophysiological effects of tobacco and smoke on ventral tegmental area dopaminergic (DA) neurons were examined in vivo in anesthetized wild-type (WT), β2-nicotinic acetylcholine receptor (nAChR) knockout (β2-/-), α4-/-, and α6-/- mice and compared with those of nicotine alone. In WT mice, smoke and nicotine had similar potentiating effects on DA cell activity, but the action of tobacco on neuronal firing was weak and often inhibitory. In particular, nicotine triggered strong bursting activity, whereas no bursting activity was observed after tobacco extract (ToE) administration. In β2-/- mice, nicotine or extract elicited no modification of the firing patterns of DA cells, indicating that extract acts predominantly through nAChRs. The differences between DA cell activation profiles induced by tobacco and nicotine alone observed in WT persisted in α6-/- mice but not in α4-/- mice. These results would suggest that tobacco has lower addiction-generating properties compared with either nicotine alone or smoke. The weak activation and prominent inhibition obtained with ToEs suggest that tobacco contains compounds that counteract some of the activating effects of nicotine and promote inhibition on DA cell acting through α4β2*-nAChRs. The nature of these compounds remains to be elucidated. It nevertheless confirms that nicotine is the main substance involved in the tobacco addiction-related activation of mesolimbic DA neurons.

摘要

尼古丁主要通过吸烟或鼻烟或咀嚼烟草来调节烟草消费的行为效应。然而,许多研究对尼古丁在这些效应中的作用提出了质疑。使用包含烟草和烟雾等所有成分的制剂可能比单独使用尼古丁更适合研究吸烟和烟草摄入的行为效应。在本研究中,在麻醉的野生型(WT)、β2-烟碱型乙酰胆碱受体(nAChR)敲除(β2-/-)、α4-/-和α6-/-小鼠体内研究了烟草和烟雾对腹侧被盖区多巴胺(DA)神经元的电生理影响,并与单独使用尼古丁进行了比较。在 WT 小鼠中,烟雾和尼古丁对 DA 细胞活动有相似的增强作用,但烟草对神经元放电的作用较弱且常常抑制。特别是,尼古丁引发强烈的爆发活动,而烟草提取物(ToE)给药后则观察不到爆发活动。在β2-/-小鼠中,尼古丁或提取物对 DA 细胞的放电模式没有引起任何改变,表明提取物主要通过 nAChRs 起作用。WT 小鼠中观察到的烟草和尼古丁单独作用引起的 DA 细胞激活谱的差异在α6-/-小鼠中持续存在,但在α4-/-小鼠中则不存在。这些结果表明,与单独的尼古丁或烟雾相比,烟草具有较低的成瘾性。ToE 获得的弱激活和明显的抑制作用表明,烟草含有一些化合物,这些化合物可以抵消尼古丁的一些激活作用,并通过α4β2*-nAChRs 促进对 DA 细胞的抑制。这些化合物的性质仍有待阐明。但这确实证实了尼古丁是参与中脑边缘多巴胺神经元与烟草成瘾相关激活的主要物质。

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