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首页> 外文期刊>Life sciences >Varenicline and nicotine enhance GABAergic synaptic transmission in rat CA1 hippocampal and medial septum/diagonal band neurons
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Varenicline and nicotine enhance GABAergic synaptic transmission in rat CA1 hippocampal and medial septum/diagonal band neurons

机译:varenicline和尼古丁增强大鼠Ca1海马和内侧隔膜/对角神经元的胃肠杆菌突触传递

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摘要

Aims The FDA approved smoking cessation aid varenicline can effectively attenuate nicotine-stimulated dopamine release. Varenicline may also exert important actions on other transmitter systems that also influence nicotine reinforcement or contribute to the drug's cognitive and affective side effects. In this study, we determined if varenicline, like nicotine, can stimulate presynaptic GABA release. Main methods Using whole-cell patch-clamp techniques, we measured GABAAR-mediated asynchronous, spontaneous miniature inhibitory postsynaptic currents (mIPSCs) in acute brain slices from two brain regions important for learning and memory, the hippocampus and basal forebrain. Key findings Both varenicline (10 ??M) and nicotine (10 ??M) applications alone resulted in small but significant increases in amplitude, as well as robustly enhanced frequency of mIPSCs in hippocampal CA1 pyramidal neurons and medial septum/diagonal band (MS/DB) neurons. A unique subpopulation of MS/DB neurons showed decreases in frequency. In the presence of nicotine, varenicline effectively attenuated the expected enhancement of hippocampal mIPSC frequency like a competitive antagonist. However, in the MS/DB, varenicline only partially attenuated nicotine's effects. Reversing the order of drug application by adding nicotine to varenicline-exposed slices had little effect. Significance Varenicline, like nicotine, stimulates presynaptic GABA release, and also exerts a partial agonist action by attenuating nicotine-stimulated release in both the hippocampus and basal forebrain. These effects could potentially affect cognitive functions. ? 2013 Elsevier Inc. All rights reserved.
机译:AIMS批准的FDA批准的吸烟戒烟助剂瓦尼尼线可以有效地衰减尼古丁刺激的多巴胺释放。 varenicline还可以对其他变送器系统发挥重要行动,这些系统也影响尼古丁强化或有助于药物的认知和情感副作用。在这项研究中,我们确定了樟树,如尼古丁,可以刺激突触前GABA释放。主要方法采用全细胞贴片技术,我们测量了GABAAR介导的异步,自发性微型抑制突触突出电流(MIPSC)在来自学习和记忆的学习和记忆,海马和基础前脑的两个脑区。主要发现两种瓦伦尼克林(10 -4 M)和烟碱(10 -4 M)单独应用导致振幅小,但显著增加,以及鲁棒地增强在海马CA1锥体神经元和中隔/交叉带mIPSC的频率(MS / dB)神经元。 MS / DB神经元的独特亚群显示出频率降低。在尼古丁存在下,振伤线有效地减弱了海马MIPSC频率的预期增强,如竞争性拮抗剂。然而,在MS / DB中,varenicline仅部分减毒尼古丁的效果。通过将尼古丁添加到樟木暴露的切片中,逆转药物申请的顺序几乎没有效果。与尼古丁一样的显着性脉冲线刺激突触前GABA释放,并且还通过在海马和基础前脑中衰减尼古丁刺激的释放来施加部分激动剂作用。这些效果可能会影响认知功能。还是2013年elsevier Inc.保留所有权利。

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