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The role of cerebellar nuclear GABAergic neurotransmission in eyeblink motor control.

机译:小脑核GABA能神经传递在眨眼运动控制中的作用。

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摘要

One of the best understood models of motor learning is the eyeblink classical conditioning paradigm in rabbits. Eyeblink conditioning relies on cerebellar circuits for the generation and expression of conditioned responses (CRs). Although these circuits have been studied extensively, their specific function is unknown and highly debated. To this end, a series of experiments were conducted to gain insight into the role of the intermediate cerebellum in the timing and retention of CRs.;The first objective of our research was to develop an accurate method to record rabbit eyeblinks. We developed an infrared, frequency modulated, non-invasive sensor with a wide-field of view. The sensor was tested against previous opto-electric, electromechanical, and video recording systems and as a result of its accuracy in eyeblink detection, this sensor was used in all subsequent experiments.;In the first group of neuropharmacological experiments, we examined the effects of inactivating the cerebellar cortical GABAergic Purkinje cell projection to the interposed nuclei (IN) on CR expression. This study successfully reconciled a long-standing controversy by documenting the dose-dependency of behavioral effects. While low doses of GABAergic blockers shortened CR latencies (short-latency responses - SLRs), the high doses of these drugs abolished CRs. In addition, low doses of GABA blockers facilitated the expression of unconditioned eyeblinks and increased eyelid closure. These data indicate that CR timing is altered only during an incomplete block of the cortical projections to the IN and that the intermediate cerebellum controls non-associative components of blinking.;The next group of experiments examined whether SLRs are triggered by cerebellum-mediated sensory information. To address this question, we inactivated the conditioned stimulus (CS)-carrying axons in the middle cerebellar peduncle (MCP) in rabbits producing SLRs. We found that blocking CS information from entering the intermediate cerebellum does in fact abolish both CRs and SLRs. This finding suggests that SLRs are cerebellum-dependent responses that are evoked by residual CS information entering the cerebellum via incompletely blocked cortical projections to the nuclei.;In the last group of experiments we tested whether the behavioral effects of MCP inactivation could be attributed to a tonic malfunction of cerebellar circuits. Classically conditioned rabbits were injected with sodium channel blocker tetrodotoxin (TTX) in the MCP while recording from cells in the interposed nuclei (IN). This treatment abolished CRs and elevated the spontaneous activity of IN neurons. Surprisingly, the CS-related modulation was not blocked and in some cases it increased. These observations suggest that normal functioning of the MCP is critical for CR expression, and the persistence of CS-related IN activity indicates that a significant portion of CS information reaches the cerebellum through pathways other than the ipsilateral MCP.
机译:运动学习的最佳理解模型之一是兔的眨眼经典条件范式。眨眼调节依赖于小脑回路来产生和表达调节反应(CR)。尽管已经对这些电路进行了广泛的研究,但是它们的具体功能仍是未知的,而且争议很大。为此,进行了一系列实验,以了解中间小脑在CR的时间和保留中的作用。我们研究的首要目标是开发一种准确的方法来记录兔的眨眼。我们开发了具有宽视野的红外,调频,无创传感器。该传感器已针对先前的光电,机电和视频记录系统进行了测试,由于其眨眼检测的准确性,该传感器已用于所有后续实验中;在第一组神经药理实验中,我们检查了使小脑皮质GABA能浦肯野细胞投射失活至CR表达的插入核(IN)。这项研究通过记录行为效应的剂量依赖性成功地解决了一个长期存在的争议。虽然低剂量的GABA能阻滞剂可缩短CR潜伏期(短时延应答-SLR),但高剂量的这些药物可消除CR。此外,低剂量的GABA阻断剂可促进无条件眨眼的表达并增加眼睑闭合。这些数据表明CR时机仅在不完整的IN皮质投影阻滞期间发生改变,并且中间小脑控制着眨眼的非关联成分。;下一组实验研究了SLR是否由小脑介导的感觉信息触发。为了解决此问题,我们灭活了产生单反的兔子中小脑梗(MCP)的带条件刺激(CS)的轴突。我们发现阻止CS信息进入中间小脑确实消除了CR和SLR。这一发现表明,单反是依赖于小脑的反应,是由残留的CS信息通过不完全阻塞的皮层投射进入核而进入小脑引起的;在最后一组实验中,我们测试了MCP失活的行为影响是否可归因于小脑回路的强直性故障。在条件条件下的兔中,在MCP中注射钠通道阻滞剂河豚毒素(TTX),同时从插入核(IN)中的细胞记录下来。这种治疗消除了CR,并提高了IN神经元的自发活动。令人惊讶的是,与CS相关的调制没有被阻止,在某些情况下它增加了。这些观察结果表明,MCP的正常功能对于CR表达至关重要,并且与CS相关的IN活性的持续存在表明,CS信息的很大一部分通过同侧MCP以外的途径到达小脑。

著录项

  • 作者单位

    Iowa State University.;

  • 授予单位 Iowa State University.;
  • 学科 Biology Neuroscience.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 152 p.
  • 总页数 152
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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