首页> 美国卫生研究院文献>The Journal of Neuroscience >Anatomical Evidence that the Superior Colliculus Controls Saccades through Central Mesencephalic Reticular Formation Gating of Omnipause Neuron Activity
【2h】

Anatomical Evidence that the Superior Colliculus Controls Saccades through Central Mesencephalic Reticular Formation Gating of Omnipause Neuron Activity

机译:解剖学证据表明上睑滤泡通过全眼神经元活动的中脑网状结构门控控制扫视

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

Omnipause neurons (OPNs) within the nucleus raphe interpositus (RIP) help gate the transition between fixation and saccadic eye movements by monosynaptically suppressing activity in premotor burst neurons during fixation, and releasing them during saccades. Premotor neuron activity is initiated by excitatory input from the superior colliculus (SC), but how the tectum's saccade-related activity turns off OPNs is not known. Since the central mesencephalic reticular formation (cMRF) is a major SC target, we explored whether this nucleus has the appropriate connections to support tectal gating of OPN activity. In dual-tracer experiments undertaken in macaque monkeys (Macaca fascicularis), cMRF neurons labeled retrogradely from injections into RIP had numerous anterogradely labeled terminals closely associated with them following SC injections. This suggested the presence of an SC–cMRF–RIP pathway. Furthermore, anterograde tracers injected into the cMRF of other macaques labeled axonal terminals in RIP, confirming this cMRF projection. To determine whether the cMRF projections gate OPN activity, postembedding electron microscopic immunochemistry was performed on anterogradely labeled cMRF terminals with antibody to GABA or glycine. Of the terminals analyzed, 51.4% were GABA positive, 35.5% were GABA negative, and most contacted glycinergic cells. In summary, a trans-cMRF pathway connecting the SC to the RIP is present. This pathway contains inhibitory elements that could help gate omnipause activity and allow other tectal drives to induce the bursts of firing in premotor neurons that are necessary for saccades. The non-GABAergic cMRF terminals may derive from fixation units in the cMRF.
机译:椎间盘中间核(RIP)内的全暂停神经元(OPN)通过单突触地抑制固定前运动爆发神经元的活动,并在扫视期间释放它们,从而帮助控制注视和眼跳运动之间的过渡。运动前神经元的活动是由上丘(SC)的兴奋性输入引起的,但是与顶盖扫视相关的活动如何关闭OPN尚不清楚。由于中央中脑网状结构(cMRF)是主要的SC靶标,我们探讨了该核是否具有适当的连接来支持OPN活性的门控门控。在猕猴(Macaca fascicularis)进行的双示踪实验中,从RIP注射中逆行标记的cMRF神经元在SC注射后具有许多与它们紧密相关的顺行标记末端。这表明存在SC–cMRF–RIP途径。此外,顺行示踪剂注入到RIP中标记为轴突末端的其他猕猴的cMRF中,证实了该cMRF预测。为了确定cMRF投影是否可以控制OPN活性,对经顺反标记的cMRF末端进行了嵌入Gem或抗GABA抗体的电子显微镜免疫化学分析。在分析的末端中,GABA阳性的占51.4%,GABA阴性的占35.5%,并且接触最多的甘氨酸能细胞。总之,存在将SC连接到RIP的跨cMRF途径。该途径包含抑制因子,这些抑制因子可能有助于门禁操作,并允许其他顶盖驱动物诱发扫视运动所必需的运动前神经元放电。非GABA能的cMRF末端可能来自cMRF中的固定单元。

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