首页> 美国卫生研究院文献>other >Nicotine-induced anxiety-like behavior in a rat model of the novelty-seeking phenotype is associated with long-lasting neuropeptidergic and neuroplastic adaptations in the amygdala: Effects of the cannabinoid receptor 1 antagonist AM251
【2h】

Nicotine-induced anxiety-like behavior in a rat model of the novelty-seeking phenotype is associated with long-lasting neuropeptidergic and neuroplastic adaptations in the amygdala: Effects of the cannabinoid receptor 1 antagonist AM251

机译:尼古丁诱导的新型寻找表型的大鼠模型中的类似焦虑行为与杏仁达拉的长期神经肽和神经塑性适应有关:大麻素受体1拮抗剂AM251的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A rat model of the novelty-seeking phenotype predicts vulnerability to the expression of behavioral sensitization to nicotine, where locomotor reactivity to novelty is used to screen experimentally-naïve rats for high (HR) versus low (LR) responders. The present study examines the long-term neuropeptidergic and neuroplastic adaptations associated with the expression of locomotor sensitization to a low dose nicotine challenge and social anxiety-like behavior following chronic intermittent nicotine exposure during adolescence in the LRHR phenotype. Our data show that the expression of behavioral sensitization to nicotine and abstinence-related anxiety are detected in nicotine pre-exposed HRs even across a long (3 wks) abstinence. Moreover, these behavioral effects of nicotine are accompanied by a persistent imbalance between neuropeptide Y and corticotrophin releasing factor systems, and a persistent increase in brain-derived neurotrophic factor (BDNF) and spinophilin mRNA levels in the amygdala. Furthermore, treatment with the cannabinoid receptor 1 antagonist, AM251 (5 mg/kg) during a short (1 wk) abstinence is ineffective in reversing nicotine-induced anxiety, fluctuations in BDNF and spinophilin mRNAs, and the neuropeptidergic dysregulations in the amygdala; although this treatment is effective in reversing the expression of locomotor sensitization to challenge nicotine even after a long abstinence. Interestingly, the identical AM251 treatment administered during the late phase of a long abstinence further augments anxiety and associated changes in BDNF and spinophilin mRNA in the basolateral nucleus of the amygdala in nicotine pre-exposed HRs. These findings implicate long-lasting neuropeptidergic and neuroplastic changes in the amygdala in vulnerability to the behavioral effects of nicotine in the novelty-seeking phenotype.
机译:寻求新奇表型的大鼠模型预测了其对尼古丁行为敏化表达的脆弱性,其中对新奇的运动反应性用于筛选初次实验的大鼠对高(HR)和低(LR)的反应者。本研究检查了与LRHR表型青春期慢性间歇性尼古丁暴露后运动对低剂量尼古丁激发和社交焦虑样行为的表达相关的长期神经肽能和神经增生适应性。我们的数据表明,即使在长期(3 wks)的禁欲中,也可以在烟碱预暴露的HR中检测到对尼古丁的行为敏感表达和与禁欲有关的焦虑。此外,尼古丁的这些行为效应伴随着神经肽Y和促肾上腺皮质激素释放因子系统之间的持续不平衡,以及杏仁核中脑源性神经营养因子(BDNF)和亲索蛋白mRNA水平的持续增加。此外,在短时(1 wk)禁欲期间用大麻素受体1拮抗剂AM251(5 mg / kg)治疗无法有效地逆转尼古丁引起的焦虑,BDNF和Spinophilin mRNA的波动以及杏仁核中的神经肽能异常。尽管这种治疗即使在长期禁欲后仍能有效逆转运动致敏性的表达,以挑战尼古丁。有趣的是,在长期禁欲的晚期给予的相同的AM251治疗进一步加剧了尼古丁暴露前HRs杏仁核基底外侧核中BDNF和Spinophilin mRNA的焦虑及相关变化。这些发现暗示着杏仁核中持久的神经肽能和神经塑性改变对新奇表型中尼古丁行为影响的脆弱性。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号