首页> 美国卫生研究院文献>Frontiers in Neural Circuits >Novel modulatory effects of neurosteroids and benzodiazepines on excitatory and inhibitory neurons excitability: a multi-electrode array recording study
【2h】

Novel modulatory effects of neurosteroids and benzodiazepines on excitatory and inhibitory neurons excitability: a multi-electrode array recording study

机译:神经甾体和苯二氮卓类药物对兴奋性和抑制性神经元兴奋性的新型调节作用:多电极阵列记录研究

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

The balance between glutamate- and GABA-mediated neurotransmission in the brain is fundamental in the nervous system, but it is regulated by the “tonic” release of a variety of endogenous factors. One such important group of molecules are the neurosteroids (NSs) which, similarly to benzodiazepines (BDZs), enhance GABAergic neurotransmission. The purpose of our work was to investigate, at in vivo physiologically relevant concentrations, the effects of NSs and BDZs as GABA modulators on dissociated neocortical neuron networks grown in long-term culture. We used a multi-electrode array (MEA) recording technique and a novel analysis that was able to both identify the action potentials of engaged excitatory and inhibitory neurons and to detect drug-induced network up-states (burst). We found that the NSs tetrahydrodeoxycorticosterone (THDOC) and allopregnanolone (ALLO) applied at low nanomolar concentrations, produced different modulatory effects on the two neuronal clusters. Conversely, at high concentrations (1 μM), both NSs, decreased excitatory and inhibitory neuron cluster excitability; however, even several hours after wash-out, the excitability of inhibitory neurons continued to be depressed, leading to a network long-term depression (LTD). The BDZs clonazepam (CLZ) and midazolam (MDZ) also decreased the network excitability, but only MDZ caused LTD of inhibitory neuron cluster. To investigate the origin of the LTD after MDZ application, we tested finasteride (FIN), an inhibitor of endogenous NSs synthesis. FIN did not prevent the LTD induced by MDZ, but surprisingly induced it after application of CLZ. The significance and possible mechanisms underlying these LTD effects of NSs and BDZs are discussed. Taken together, our results not only demonstrate that ex vivo networks show a sensitivity to NSs and BDZs comparable to that expressed in vivo, but also provide a new global in vitro description that can help in understanding their activity in more complex systems.
机译:谷氨酸和GABA介导的神经传递在大脑中的平衡在神经系统中是基本的,但它受多种内源性因素的“强直”释放所调节。这样一个重要的分子组是神经固醇(NSs),与苯二氮卓类(BDZs)类似,它们能增强GABA能神经传递。我们的工作目的是在体内生理相关浓度下研究作为GABA调节剂的NSs和BDZs对长期培养的游离新皮质神经元网络的影响。我们使用了多电极阵列(MEA)记录技术和新颖的分析方法,能够识别参与的兴奋性和抑制性神经元的动作电位,并能够检测药物诱导的网络向上状态(爆发)。我们发现以低纳摩尔浓度应用的NSs四氢脱氧皮质酮(THDOC)和Allopregnanolone(ALLO)对两个神经元簇产生不同的调节作用。相反,在高浓度(1μM)下,两个NS均会降低兴奋性和抑制性神经元簇的兴奋性;然而,即使在冲洗后数小时,抑制性神经元的兴奋性仍持续下降,导致网络长期抑制(LTD)。 BDZ的氯硝西am(CLZ)和咪达唑仑(MDZ)也降低了网络兴奋性,但只有MDZ引起LTD抑制神经元簇。为了研究MDZ应用后LTD的起源,我们测试了非那雄胺(FIN),它是内源性NSs合成的抑制剂。 FIN并不能阻止MDZ诱导的LTD,但是出人意料的是在CLZ应用后诱导了LTD。讨论了NS和BDZ的这些LTD效应的重要性和可能的​​机制。两者合计,我们的结果不仅表明离体网络对NSs和BDZs的敏感性与在体内表达的相当,而且提供了新的全球性体外描述,可帮助理解它们在更复杂系统中的活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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