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视觉体验可防止成年上丘中GABAB受体依赖性短期抑制的失调。

Visual experience prevents dysregulation of GABAB receptor-dependent short-term depression in adult superior colliculus.

作者信息

Balmer Timothy S, Pallas Sarah L

机构信息

Neuroscience Institute, Georgia State University, Atlanta, Georgia.

Neuroscience Institute, Georgia State University, Atlanta, Georgia

出版信息

J Neurophysiol. 2015 Apr 1;113(7):2049-61. doi: 10.1152/jn.00882.2014. Epub 2015 Jan 7.

Abstract

Progressive loss of plasticity during development prevents refined circuits from regressing to an immature state and is thought to depend on maturation of GABAergic inhibition. For example, a gradual reduction in size of visual receptive fields (RFs) occurs in the superior colliculus (SC) during development. Maintenance of the refined state throughout adulthood requires early light exposure. Here we investigate the potential role of changes in long- or short-term plasticity in experience-dependent maintenance of refined RFs. Using an acute SC slice preparation, we found that long-term plasticity was not affected by visual deprivation, indicating that it does not underlie deprivation-induced RF enlargement. In contrast, visual deprivation altered short-term plasticity in an unexpected way. Specifically, GABAB receptor (GABABR)-mediated paired pulse depression was increased in slices from dark-reared animals. This increase was mimicked by GABAAR blockade in slices from normally reared animals, suggesting that experience-dependent maintenance of GABAAR function prevents an increase in probability of neurotransmitter release. GABABR-mediated short-term depression in response to strong stimulation (such as occurs during vision) was reduced in slices from dark-reared animals. This change was mimicked in slices from normal animals by reducing GABA release. These results are consistent with the hypothesis that early visual experience maintains GABAergic inhibition and prevents later deprivation-induced alterations of short-term depression in SC. Identifying how plasticity is restricted in mature circuits could guide therapies to enhance recovery of function in adults.

摘要

发育过程中可塑性的逐渐丧失可防止精细的神经回路退回到不成熟状态,并且被认为依赖于γ-氨基丁酸(GABA)能抑制的成熟。例如,在发育过程中,上丘(SC)的视觉感受野(RFs)大小会逐渐减小。在整个成年期维持精细状态需要早期光照暴露。在这里,我们研究长期或短期可塑性变化在依赖经验维持精细RFs中的潜在作用。使用急性SC脑片制备,我们发现长期可塑性不受视觉剥夺的影响,这表明它不是剥夺诱导的RF扩大的基础。相反,视觉剥夺以一种意想不到的方式改变了短期可塑性。具体而言,在黑暗饲养动物的脑片中,GABAB受体(GABABR)介导的双脉冲抑制增强。在正常饲养动物的脑片中,GABA A受体(GABAAR)阻断可模拟这种增强,这表明依赖经验维持GABAAR功能可防止神经递质释放概率增加。在黑暗饲养动物的脑片中,对强刺激(如视觉过程中发生的刺激)的GABABR介导的短期抑制减弱。在正常动物的脑片中,通过减少GABA释放可模拟这种变化。这些结果与以下假设一致:早期视觉经验维持GABA能抑制,并防止后期剥夺诱导的SC短期抑制改变。确定成熟神经回路中可塑性如何受到限制,可为增强成人功能恢复的治疗提供指导。

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