首页> 外文期刊>Neuroscience Research: The Official Journal of the Japan Neuroscience Society >Field potential recording in the ventral tegmental area: Pharmacological and toxicological evaluations of postsynaptic dopaminergic neuron activity.
【24h】

Field potential recording in the ventral tegmental area: Pharmacological and toxicological evaluations of postsynaptic dopaminergic neuron activity.

机译:腹侧被盖区的田间电势记录:突触后多巴胺能神经元活性的药理和毒理学评估。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Addictive drugs and psychologic stress influence the input strength of ventral tegmental area (VTA) neurons, which implies the involvement of synaptic plasticity in dopaminergic neurons. Properties of excitatory synaptic transmission to the dopaminergic neurons have been analyzed using intracellular and patch-clamp recording methods. In the present study, we attempted to establish the field recording procedure in VTA slice preparations to monitor excitatory synaptic transmission. We evaluated this procedure using slice preparations from 6-hydroxydopamine (6-OHDA)-treated animals. In horizontal slices containing the VTA, electrical stimulation of anterior afferent fibers produced two distinct negative field potentials, presumably a fiber volley component and a transsynaptic component. Pharmacological analysis revealed that the transsynaptic component was composed of bicuculline-sensitive and CNQX-sensitive components. Neonatal 6-OHDA administration reduced approximately 90% of tyrosine hydroxylase expression in the VTA and eliminated more than 50% of the transsynaptic components. This result suggests that at least 50% of the observed transsynaptic component reflected the postsynaptic responses of the dopaminergic neurons.
机译:上瘾的药物和心理压力会影响腹侧被盖区(VTA)神经元的输入强度,这意味着多巴胺能神经元中突触可塑性的参与。兴奋性突触传递到多巴胺能神经元的属性已使用细胞内和膜片钳记录方法进行了分析。在本研究中,我们试图建立VTA切片制备中的现场记录程序,以监测兴奋性突触传递。我们使用来自6-羟基多巴胺(6-OHDA)处理的动物的切片制剂评估了该程序。在包含VTA的水平切片中,对前传入纤维的电刺激产生了两个截然不同的负电场电势,大概是纤维齐射成分和突触成分。药理学分析表明,突触成分由双小分子敏感和CNQX敏感成分组成。新生儿使用6-OHDA可以减少VTA中约90%的酪氨酸羟化酶表达,并消除超过50%的突触成分。该结果表明,至少观察到的突触成分的50%反映了多巴胺能神经元的突触后反应。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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