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GABA-A 受体调节剂可改变持续性焦虑动物模型的情绪和海马θ节律。

GABA-A receptor modulators alter emotionality and hippocampal theta rhythm in an animal model of long-lasting anxiety.

机构信息

Laboratory of Neuropharmacology, Department of Pharmacology, Center of Biological Sciences (CCB), Federal University of Santa Catarina (UFSC), Florianópolis, SC 88049-900, Brazil.

出版信息

Brain Res. 2013 Sep 26;1532:21-31. doi: 10.1016/j.brainres.2013.07.045. Epub 2013 Aug 1.

Abstract

The cholinergic system is implicated in emotional regulation. The injection of non-convulsant doses of the muscarinic receptor agonist pilocarpine (PILO) induces long-lasting anxiogenic responses in rats evaluated at different time-points (24h to 3 months). To investigate the underlying mechanisms, rats treated with PILO (150mg/kg) were injected 24h or 1 month later with an anxiolytic (diazepam, 1mg/kg, DZP) or anxiogenic (pentylenetetrazole, 15mg/kg, PTZ) drug and evaluated in the elevated plus-maze (EPM). Prefrontal cortex (PFC) and hippocampal (HIP) electroencephalographic recordings and acetylcolinesterase (AChE) activity were also analyzed after PILO treatment. Anxiogenic responses observed in the EPM 24h or 1 month after PILO treatment (e.g., decreased time spent and number of entries into the open arms of the maze) were blocked by DZP but not affected by PTZ. No epileptiform events were registered in the HIP or PFC at 24h or 1 month after PILO injection, but enhanced theta activity was observed in the HIP. DZP decreased hippocampal theta of PILO-treated rats in contrast with PTZ, which increased this parameter in saline- and PILO-treated rats. The HIP and PFC AChE activity did not change after PILO treatment. Our findings demonstrate that the long-term effects on the emotionality of rats induced by PILO are associated with electrophysiological changes in the HIP and sensitive to pharmacological manipulation of the GABAergic system. The present work may support this new research model of long-lasting anxiety, while also highlighting the muscarinic system as a potential target involved in anxiety disorders.

摘要

胆碱能系统参与情绪调节。在不同时间点(24 小时至 3 个月)评估时,向大鼠注射非惊厥剂量的毒蕈碱受体激动剂毛果芸香碱(PILO)会引起持久的焦虑反应。为了研究潜在的机制,在注射 PILO(150mg/kg)24 小时或 1 个月后,用抗焦虑药(地西泮,1mg/kg,DZP)或致焦虑药(戊四氮,15mg/kg,PTZ)处理大鼠,并在高架十字迷宫(EPM)中进行评估。还分析了 PILO 处理后前额叶皮层(PFC)和海马(HIP)的脑电图记录和乙酰胆碱酯酶(AChE)活性。PILO 处理后 24 小时或 1 个月在 EPM 中观察到的焦虑反应(例如,进入迷宫开放臂的时间和次数减少)被 DZP 阻断,但不受 PTZ 影响。在 PILO 注射后 24 小时或 1 个月,HIP 或 PFC 中未记录到癫痫样事件,但观察到 HIP 中增强的θ活动。与 PTZ 相反,DZP 降低了 PILO 处理大鼠的海马θ,而 PTZ 增加了生理盐水和 PILO 处理大鼠的该参数。PILO 处理后,HIP 和 PFC 的 AChE 活性没有变化。我们的研究结果表明,PILO 对大鼠情绪的长期影响与 HIP 的电生理变化有关,并对 GABA 能系统的药理学操作敏感。本工作可能支持这种新的持久焦虑研究模型,同时强调毒蕈碱系统作为涉及焦虑症的潜在靶标。

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