青春期小脑核操作可独立改变雌雄小鼠的反向学习和神经周围网络强度。

IF 4.4 2区 医学 Q1 NEUROSCIENCES
Tristan T Lyle, Jessica L Verpeut
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引用次数: 0

摘要

小脑,在认知和社会行为中被认为是活跃的,通过小脑核(CN)和丘脑到皮质区域具有多突触连接,但这些通路的形成和调节尚未完全了解。神经周围网络(PNNs)响应局部细胞活动的变化,并在发育过程中出现。pnn与学习和神经发育障碍有关,但其在发育过程中的作用尚不清楚。在自闭症谱系障碍(ASD)患者中发现了连通性缺陷,特别是在外侧神经网络(LCN)-皮质区域之间,患者表现出认知灵活性降低。为了研究LCN在认知中的作用,从出生后21-35天开始,在雄性和雌性小鼠中使用设计物药物特异性激活的设计物受体(DREADDs)来干扰神经活动。我们发现,虽然青少年LCN中断不改变任务习得,但正确的选择反转表现依赖于DREADD操作和性别。与对照组相比,抑制性dreadd改善了男性的反转学习(比标准快5天),兴奋性dreadd改善了女性的反转学习(比标准快10天)。有趣的是,在女性中,无论方向如何,DREADDS操作都会降低PNN强度,而在男性中,只有抑制性DREADDS会降低PNN。这表明慢性青少年LCN操作可能在PNN结构和LCN输出中有性别特异性代偿性变化,以改善反转学习。本研究为LCN在非运动功能、行为和可塑性上的性别依赖性差异提供了新的证据。小脑通常被认为对运动控制很重要;然而,最近的研究揭示了它在认知中的作用。然而,目前尚不清楚小脑是否在早期发育中调节认知,或者这种影响可能通过何种途径发挥作用。利用化学发生方法,我们对青春期雄性和雌性小鼠的小脑外侧核进行了操作。通过对触屏任务的反向学习来测量的灵活认知以性别依赖的方式改变。研究发现,小脑核抑制小鼠的神经网络减少,这些小鼠表现出更快的逆转学习。这些发现强调了研究小脑核对获得早期发育的新见解的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adolescent Cerebellar Nuclei Manipulation Alters Reversal Learning and Perineuronal Net Intensity Independently in Male and Female Mice.

The cerebellum, identified to be active during cognitive and social behavior, has multisynaptic connections through the cerebellar nuclei (CN) and thalamus to cortical regions, yet formation and modulation of these pathways are not fully understood. Perineuronal nets (PNNs) respond to changes in local cellular activity and emerge during development. PNNs are implicated in learning and neurodevelopmental disorders, but their role in the CN during development is unknown. Connectivity deficits, specifically between lateral CN (LCN) and cortical regions have been found in autism spectrum disorder with patients displaying reduced cognitive flexibility. To examine the role of LCN on cognition, neural activity was perturbed in both male and female mice using designer receptors exclusively activated by designer drugs (DREADDs) from postnatal day 21 to 35. We found that while an adolescent LCN disruption did not alter task acquisition, correct choice reversal performance was dependent on DREADD manipulation and sex. Inhibitory DREADDs improved reversal learning in males (5 d faster to criteria), and excitatory DREADDs improved female reversal learning (10 d faster to criteria) compared with controls. Interestingly, the DREADD manipulation in females regardless of direction reduced PNN intensity, whereas in males, only the inhibitory DREADDs reduced PNNs. This suggests a chronic adolescent LCN manipulation may have sex-specific compensatory changes in PNN structure and LCN output to improve reversal learning. This study provides new evidence for LCN in nonmotor functions and sex-dependent differences in behavior and CN plasticity.

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来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
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