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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >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.
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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.

机译:扁桃体中央核或末梢纹床核中烟碱样乙酰胆碱或多巴胺D1样受体的阻滞不会促使尼古丁依赖性大鼠中尼古丁戒断。

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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.
机译:大约70%的吸烟者希望戒烟,但尝试的部分原因通常是不成功的,原因是厌恶的尼古丁戒断综合征。我们调查了烟酸和多巴胺能信号在杏仁核中央核(CeA)和纹状体末端背外侧床核(dlBNST)可能参与大鼠沉淀的尼古丁戒断样的无快感抑郁症中的可能参与。与尼古丁依赖的大鼠在停止慢性尼古丁给药(自发戒断)或全身或腹侧被盖区(VTA)后,与对照组相比,颅内自我刺激(ICSS)阈值升高,但在核内伏隔(NAcc)中没有升高,在暴露于尼古丁(沉淀戒断)时给予烟碱乙酰胆碱受体(nAchR)拮抗剂。我们检查了是否在大脑中将nAChR拮抗剂二氢-β-类胡萝卜素(DHbetaE; 0.6-20微克总双边剂量)或多巴胺D1样受体拮抗剂SCH 23390(2-16微克总双边剂量)施用到CeA和dlBNST结果中尼古丁治疗大鼠的戒断样阈值升高。 CeA或dlBNST中的烟碱乙酰胆碱和D1样受体阻滞剂不会在烟碱和盐处理的大鼠中引起差异性阈值升高。此外,在盐水和尼古丁治疗的大鼠中,注入dlBNST而不是CeA的最高SCH 23390剂量(16微克双边剂量)同样升高了阈值,这表明dlBNST中的多巴胺能信号传导可能会调节基线以下的大脑奖励功能条件。这些结果表明,CeA和dlBNST中的nACh和D1样信号传导不会随着尼古丁依赖的发展而发生神经适应,而尼古丁依赖可能与尼古丁戒断的抑郁样方面有关。

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