色素性视网膜炎
神经科学
视皮层
神经退行性变
视网膜变性
视网膜
生物
视网膜
神经可塑性
眼科
医学
病理
疾病
作者
Tatjana Begenisic,Raffaele Mazziotti,Giulia Sagona,Leonardo Lupori,Alessandro Sale,Lucia Galli,Laura Baroncelli
出处
期刊:Neuroscience
[Elsevier]
日期:2020-01-01
卷期号:424: 205-210
被引量:14
标识
DOI:10.1016/j.neuroscience.2019.10.045
摘要
Retinitis Pigmentosa (RP) is a class of inherited disorders caused by the progressive death of photoreceptors in the retina. RP is still orphan of an effective treatment, with increasing optimism deriving from research aimed at arresting neurodegeneration or replacing light-responsive elements. All these therapeutic strategies rely on the functional integrity of the visual system downstream of photoreceptors. Whereas the inner retinal structure and optic radiation are known to be considerably preserved at least in early stages of RP, very little is known about the visual cortex. Remarkably, it remains completely unclear whether visual cortex plasticity is still present in RP. Using a well-established murine model of RP, the rd10 mouse, we report that visual cortical circuits retain high levels of plasticity, preserving their capability of input-dependent remodelling even at a late stage of retinal degeneration.
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