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阻断杏仁核中央核或终纹床核中的烟碱型乙酰胆碱受体或多巴胺D1样受体,不会使尼古丁依赖大鼠出现尼古丁戒断症状。

Blockade of nicotinic acetylcholine or dopamine D1-like receptors in the central nucleus of the amygdala or the bed nucleus of the stria terminalis does not precipitate nicotine withdrawal in nicotine-dependent rats.

作者信息

Jonkman Sietse, Markou Athina

机构信息

Molecular and Integrative Neurosciences Department, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Neurosci Lett. 2006 May 29;400(1-2):140-5. doi: 10.1016/j.neulet.2006.02.030. Epub 2006 Mar 23.

Abstract

Approximately 70% of tobacco smokers wish to quit, but attempts are often unsuccessful partly due to the aversive nicotine withdrawal syndrome. We investigated the possible involvement of nicotinic and dopaminergic signalling in the central nucleus of the amygdala (CeA) and dorsolateral bed nucleus of the stria terminalis (dlBNST) in the anhedonic depression-like effect of precipitated nicotine withdrawal in rats. Nicotine-dependent rats exhibit elevations in intracranial self-stimulation (ICSS) thresholds compared to control rats after cessation of chronic nicotine administration (spontaneous withdrawal) or systemic or intra-ventral tegmental area (VTA), but not intra-nucleus accumbens (NAcc), administration of nicotinic acetylcholine receptor (nAchR) antagonists while exposed to nicotine (precipitated withdrawal). We examined whether intracerebral administration of the nAChR antagonist dihydro-beta-erythroidine (DHbetaE; 0.6-20 microg total bilateral dose) or the dopamine D1-like receptor antagonist SCH 23390 (2-16 microg total bilateral dose) into the CeA and dlBNST results in withdrawal-like threshold elevations in nicotine-treated rats. Nicotinic acetylcholine and D1-like receptor blockade in the CeA or the dlBNST did not induce differential threshold elevations in nicotine- and saline-treated rats. Further, the highest SCH 23390 dose (16 microg bilateral dose) injected into the dlBNST, but not the CeA, elevated thresholds similarly in both saline- and nicotine-treated rats, suggesting that dopaminergic signalling in the dlBNST may regulate brain reward function under baseline conditions. These results suggest that nACh and D1-like signalling in the CeA and the dlBNST does not develop neuroadaptations with the development of nicotine dependence that may be involved in the depression-like aspects of nicotine withdrawal.

摘要

大约70%的吸烟者希望戒烟,但由于令人厌恶的尼古丁戒断综合征,戒烟尝试往往不成功。我们研究了烟碱能和多巴胺能信号在杏仁核中央核(CeA)和终纹床核背外侧核(dlBNST)中可能的参与情况,这些脑区与大鼠尼古丁戒断诱发的快感缺失样抑郁效应有关。与对照大鼠相比,尼古丁依赖大鼠在慢性尼古丁给药停止后(自发戒断),或在暴露于尼古丁时全身或腹侧被盖区(VTA)而非伏隔核(NAcc)注射烟碱型乙酰胆碱受体(nAchR)拮抗剂后,颅内自我刺激(ICSS)阈值升高(诱发戒断)。我们研究了向CeA和dlBNST脑内注射nAChR拮抗剂二氢-β-刺桐啶(DHbetaE;双侧总剂量0.6 - 20微克)或多巴胺D1样受体拮抗剂SCH 23390(双侧总剂量2 - 16微克)是否会导致尼古丁处理大鼠出现类似戒断的阈值升高。CeA或dlBNST中的烟碱型乙酰胆碱和D1样受体阻断在尼古丁处理和生理盐水处理的大鼠中均未诱导出不同的阈值升高。此外,注射到dlBNST而非CeA中的最高剂量SCH 23390(双侧剂量16微克)在生理盐水处理和尼古丁处理的大鼠中均同样升高了阈值,这表明dlBNST中的多巴胺能信号可能在基线条件下调节大脑奖赏功能。这些结果表明,CeA和dlBNST中的nACh和D1样信号不会随着尼古丁依赖的发展而产生可能与尼古丁戒断的抑郁样方面有关的神经适应性变化。

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