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金鱼视网膜顶盖投射再生过程中的长时程增强和活动依赖性视网膜定位锐化:共同敏感期及对NMDA受体拮抗剂的敏感性

Long-term potentiation and activity-dependent retinotopic sharpening in the regenerating retinotectal projection of goldfish: common sensitive period and sensitivity to NMDA blockers.

作者信息

Schmidt J T

机构信息

Department of Biological Sciences, State University of New York, Albany 12222.

出版信息

J Neurosci. 1990 Jan;10(1):233-46. doi: 10.1523/JNEUROSCI.10-01-00233.1990.

Abstract

The regenerating retinotectal projection in goldfish goes through an activity-driven refinement that appears to involve the elimination of inappropriate branches from early arbors. Retinotopically appropriate branches may be stabilized because the normally correlated firing of neighboring ganglion cells causes summation of their postsynaptic responses and increases their effectiveness by a Hebbian mechanism. In this study, I report that the regenerating projection has an increased capacity for long-term potentiation (LTP) that may be related to the activity-driven sharpening. In the normal projection, field potentials, reflecting currents from EPSPs elicited by optic nerve shock, are large (greater than 4 mV) and very stable. In newly regenerated projections, field potentials are initially small (less than 1 mV), but a train of 20 stimuli at 0.1 Hz results in a large (100-200%) increase in amplitude that is stable for at least 8 hr, and in 3 cases overnight. The capacity for potentiation is greatest from 20 to 40 d postcrush, the time just after arrival of the optic fibers, and during the period of retinotopic sharpening. A greater-than-normal capacity for potentiation persists for many months. Topical application of NMDA receptor blockers AP5 or AP7 at 25 microM prevents potentiation without decrementing ongoing responses. The closely related agent AP6, which is not an NMDA receptor blocker, does not prevent potentiation. In addition, infusion of the NMDA receptor blockers AP5 or AP7 into the tectal ventricle (4 microliters/d of 500 microM solution) for 2-3 weeks during regeneration prevented retinotopic sharpening, as assessed by electrophysiological mapping. At each tectal point, responsive areas in the visual field were enlarged to 28 degrees vs 11-12 degrees in control regenerates and normals. This was comparable to data from fish regenerating with activity blocked with intraocular tetrodotoxin or synchronized by stroboscopic illumination and indicates uncorrected errors in targeting of regenerated arbors (Schmidt, 1985). The results support the involvement of NMDA receptors in sharpening and suggest that the initial step in stabilizing appropriate branches may be a long-lasting increase in synaptic gain.

摘要

金鱼视网膜-顶盖投射的再生过程会经历一个由活动驱动的精细化过程,这一过程似乎涉及到消除早期树突中不适当的分支。视网膜拓扑结构合适的分支可能会得到稳定,因为相邻神经节细胞通常具有相关性的放电会导致它们突触后反应的总和,并通过赫布机制提高其有效性。在本研究中,我报告再生投射具有增强的长时程增强(LTP)能力,这可能与活动驱动的精细化有关。在正常投射中,反映视神经冲击诱发的兴奋性突触后电位(EPSP)电流的场电位很大(大于4 mV)且非常稳定。在新再生的投射中,场电位最初很小(小于1 mV),但以0.1 Hz频率施加20次刺激会导致幅度大幅增加(100 - 200%),且至少在8小时内保持稳定,在3个案例中甚至持续过夜。增强能力在挤压后20至40天最大,这是视神经纤维刚到达后的时间,也是视网膜拓扑精细化的时期。增强能力高于正常水平的状态会持续数月。局部应用25 microM的NMDA受体阻滞剂AP5或AP7可阻止增强,且不会降低正在进行的反应。密切相关的试剂AP6不是NMDA受体阻滞剂,不会阻止增强。此外,在再生过程中,将NMDA受体阻滞剂AP5或AP7注入顶盖脑室(500 microM溶液,每天4微升)持续2 - 3周可阻止视网膜拓扑精细化,这通过电生理图谱评估得出。在每个顶盖点,视野中的反应区域扩大到了28度,而对照再生鱼和正常鱼中的反应区域为11 - 12度。这与用眼内河豚毒素阻断活动或通过频闪照明同步活动的再生鱼的数据相当,表明再生树突在靶向定位上存在未校正的误差(施密特,1985年)。这些结果支持NMDA受体参与精细化过程,并表明稳定合适分支的初始步骤可能是突触增益的持久增加。

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