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Smoke Extracts and Nicotine but not Tobacco Extracts Potentiate Firing and Burst Activity of Ventral Tegmental Area Dopaminergic Neurons in Mice

机译:烟雾提取物和尼古丁而不是烟草提取物会增强小鼠腹侧被盖区多巴胺能神经元的生火和爆发活性

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摘要

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.
机译:尼古丁可通过吸烟或通过鼻烟或咀嚼来吸烟,从而显着调节烟草消费的行为影响。但是,许多研究质疑尼古丁在这些作用中的排他性作用。使用含有烟草所有成分的制剂(例如烟草和烟雾提取物)可能比单独使用尼古丁更适合于研究吸烟和烟草摄入的行为影响。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-/-),体内麻醉下检查了烟草和烟雾对腹侧被盖区多巴胺能(DA)神经元的电生理作用,将α4-/-和α6-/-小鼠与单独的尼古丁进行比较。在野生型小鼠中,烟和尼古丁对DA细胞活性具有类似的增强作用,但烟草对神经元放电的作用较弱,通常具有抑制作用。特别是,尼古丁触发了强烈的爆发活性,而在服用烟草提取物(ToE)后未观察到爆发活性。在β2-/-小鼠中,尼古丁或提取物未引起DA细胞放电模式的改变,表明提取物主要通过nAChRs起作用。在WT中观察到的仅由烟草和尼古丁诱导的DA细胞活化分布之间的差异在α6-/-小鼠中持续存在,而在α4-/-小鼠中不存在。这些结果表明,与单独使用尼古丁或吸烟相比,烟草具有较低的成瘾性。 ToEs的弱激活和显着抑制作用表明,烟草中包含的化合物可抵消尼古丁的某些激活作用,并促进通过α4β2 * -nAChRs对DA细胞的抑制作用。这些化合物的性质尚待阐明。但是,它证实尼古丁是与烟草成瘾相关的中脑边缘DA神经元活化的主要物质。

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