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本文引用的文献

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Acquisition, extinction, and reacquisition of a cerebellar cortical memory trace.小脑皮质记忆痕迹的获取、消退和重新获取。
J Neurosci. 2007 Mar 7;27(10):2493-502. doi: 10.1523/JNEUROSCI.4202-06.2007.
2
Climbing fiber discharge regulates cerebellar functions by controlling the intrinsic characteristics of purkinje cell output.攀缘纤维放电通过控制浦肯野细胞输出的内在特性来调节小脑功能。
J Neurophysiol. 2007 Apr;97(4):2590-604. doi: 10.1152/jn.00627.2006. Epub 2007 Jan 31.
3
Motor deficits in homozygous and heterozygous p/q-type calcium channel mutants.纯合子和杂合子p/q型钙通道突变体中的运动缺陷。
J Neurophysiol. 2007 Feb;97(2):1280-7. doi: 10.1152/jn.00322.2006. Epub 2006 Sep 27.
4
alphaCaMKII Is essential for cerebellar LTD and motor learning.α钙调蛋白激酶II对小脑长时程抑制和运动学习至关重要。
Neuron. 2006 Sep 21;51(6):835-43. doi: 10.1016/j.neuron.2006.08.013.
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Selective engagement of plasticity mechanisms for motor memory storage.用于运动记忆存储的可塑性机制的选择性参与。
Neuron. 2006 Sep 21;51(6):823-34. doi: 10.1016/j.neuron.2006.08.026.
6
Climbing fiber-evoked endocannabinoid signaling heterosynaptically suppresses presynaptic cerebellar long-term potentiation.攀爬纤维诱发的内源性大麻素信号通过异突触抑制突触前小脑长时程增强。
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Involvement of basal protein kinase C and extracellular signal-regulated kinase 1/2 activities in constitutive internalization of AMPA receptors in cerebellar Purkinje cells.基础蛋白激酶C和细胞外信号调节激酶1/2活性参与小脑浦肯野细胞中AMPA受体的组成型内化。
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8
Neuroscience and learning: lessons from studying the involvement of a region of cerebellar cortex in eyeblink classical conditioning.神经科学与学习:从小脑皮质一个区域参与眨眼经典条件反射的研究中获得的启示
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Purkinje cell activity during classical eyeblink conditioning in decerebrate guinea pigs.去大脑豚鼠经典眨眼条件反射过程中的浦肯野细胞活动
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10
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.浦肯野细胞中FMR1基因的缺失会增强平行纤维长时程抑制,增大棘突,并减弱脆性X综合征中的小脑眼睑条件反射。
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在向小脑浦肯野细胞输入多条攀缘纤维的小鼠中,前庭眼反射的运动学习受损。

Impaired motor learning in the vestibulo-ocular reflex in mice with multiple climbing fiber input to cerebellar Purkinje cells.

作者信息

Kimpo Rhea R, Raymond Jennifer L

机构信息

Department of Neurobiology, Stanford University, Stanford, California 94305-5125, USA.

出版信息

J Neurosci. 2007 May 23;27(21):5672-82. doi: 10.1523/JNEUROSCI.0801-07.2007.

DOI:10.1523/JNEUROSCI.0801-07.2007
PMID:17522312
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6672772/
Abstract

A unique feature of the cerebellar architecture is that Purkinje cells in the cerebellar cortex each receive input from a single climbing fiber. In mice deficient in the gamma isoform of protein kinase C (PKCgamma-/- mice), this normal architecture is disrupted so that individual Purkinje cells receive input from multiple climbing fibers. These mice have no other known abnormalities in the cerebellar circuit. Here, we show that PKCgamma-/- mice are profoundly impaired in vestibulo-ocular reflex (VOR) motor learning. The PKCgamma-/- mice exhibited no adaptive increases or decreases in VOR gain at training frequencies of 2 or 0.5 Hz. This impairment was present across a broad range of peak retinal slip speeds during training. We compare the results for VOR motor learning with previous studies of the performance of PKCgamma-/- mice on other cerebellum-dependent learning tasks. Together, the results suggest that single climbing fiber innervation of Purkinje cells is critical for some, but not all, forms of cerebellum-dependent learning, and this may depend on the region of the cerebellum involved, the organization of the relevant neural circuits downstream of the cerebellar cortex, as well as the timing requirements of the learning task.

摘要

小脑结构的一个独特特征是,小脑皮质中的浦肯野细胞各自仅接收来自一条攀爬纤维的输入。在蛋白激酶Cγ亚型缺乏的小鼠(PKCγ-/-小鼠)中,这种正常结构被破坏,使得单个浦肯野细胞接收来自多条攀爬纤维的输入。这些小鼠在小脑回路中没有其他已知的异常。在此,我们表明PKCγ-/-小鼠在前庭眼反射(VOR)运动学习方面严重受损。PKCγ-/-小鼠在2Hz或0.5Hz的训练频率下,VOR增益没有适应性增加或降低。在训练期间的广泛峰值视网膜滑动速度范围内均存在这种损伤。我们将VOR运动学习的结果与先前关于PKCγ-/-小鼠在其他小脑依赖学习任务中的表现的研究进行比较。综合来看,结果表明浦肯野细胞的单攀爬纤维支配对于某些(但不是所有)形式的小脑依赖学习至关重要,这可能取决于所涉及的小脑区域、小脑皮质下游相关神经回路的组织,以及学习任务的时间要求。