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脆性X综合征中由于皮质血管活性肠肽中间神经元调节功能丧失导致对干扰物超敏反应。

Hypersensitivity to distractors in Fragile X syndrome from loss of modulation of cortical VIP interneurons.

作者信息

Rahmatullah Noorhan, Schmitt Lauren M, De Stefano Lisa, Post Sam, Robledo Jessica, Chaudhari Gunvant R, Pedapati Ernest, Erickson Craig A, Portera-Cailliau Carlos, Goel Anubhuti

机构信息

Neuroscience Graduate Program, UC Riverside, CA.

Department of Psychology, UC Riverside, CA.

出版信息

bioRxiv. 2023 Jan 3:2023.01.03.522654. doi: 10.1101/2023.01.03.522654.

Abstract

Attention deficit is one of the most prominent and disabling symptoms in Fragile X Syndrome (FXS). Hypersensitivity to sensory stimuli contributes to attention difficulties by overwhelming and/or distracting affected individuals, which disrupts activities of daily living at home and learning at school. We find that auditory or visual distractors selectively impair visual discrimination performance in both humans and mice with FXS, but not their typically developing controls. Vasoactive intestinal polypeptide (VIP) neurons were significantly modulated by incorrect responses in the post-stimulus period during early distractor trials in WT mice, consistent with their known role as 'error' signals. Strikingly, however, VIP cells from mice showed little modulation in error trials, and this correlated with their poor performance on the distractor task. Thus, VIP interneurons and their reduced modulatory influence on pyramidal cells, could be a potential therapeutic target for attentional difficulties in FXS.

摘要

注意力缺陷是脆性X综合征(FXS)最突出且致残的症状之一。对感觉刺激的超敏反应通过使受影响个体不堪重负和/或分散注意力,导致注意力困难,从而扰乱在家中的日常生活活动和在学校的学习。我们发现,听觉或视觉干扰因素会选择性地损害患有FXS的人类和小鼠的视觉辨别能力,但不会影响其发育正常的对照组。在野生型小鼠早期干扰试验的刺激后阶段,血管活性肠肽(VIP)神经元会因错误反应而受到显著调节,这与其作为“错误”信号的已知作用一致。然而,令人惊讶的是,患有FXS的小鼠的VIP细胞在错误试验中几乎没有受到调节,这与其在干扰任务中的糟糕表现相关。因此,VIP中间神经元及其对锥体细胞调节影响的减弱,可能是FXS注意力困难的一个潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d0e/9881942/215f6a721810/nihpp-2023.01.03.522654v1-f0001.jpg

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