Adolescent Thalamoprefrontal Inhibition Leads to Changes in Intrinsic Prefrontal Network Connectivity.

IF 2.7 3区 医学 Q3 NEUROSCIENCES
eNeuro Pub Date : 2024-08-29 Print Date: 2024-08-01 DOI:10.1523/ENEURO.0284-24.2024
David Petersen, Ricardo Raudales, Ariadna Kim Silva, Christoph Kellendonk, Sarah Canetta
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Abstract

Adolescent inhibition of thalamocortical projections from postnatal days P20 to 50 leads to long-lasting deficits in prefrontal cortex function and cognition in the adult mouse. While this suggests a role of thalamic activity in prefrontal cortex maturation, it is unclear how inhibition of these projections affects prefrontal circuitry during adolescence. Here, we used chemogenetic tools to inhibit thalamoprefrontal projections in male/female mice from P20 to P35 and measured synaptic inputs to prefrontal pyramidal neurons by layer (either II/III or V/VI) and projection target (mediodorsal thalamus (MD), nucleus accumbens (NAc), or callosal prefrontal projections) 24 h later using slice physiology. We found a decrease in the frequency of excitatory and inhibitory currents in layer II/III NAc and layer V/VI MD-projecting neurons while layer V/VI NAc-projecting neurons showed an increase in the amplitude of excitatory and inhibitory currents. Regarding cortical projections, the frequency of inhibitory but not excitatory currents was enhanced in contralateral mPFC-projecting neurons. Notably, despite these complex changes in individual levels of excitation and inhibition, the overall balance between excitation and inhibition in each cell was only altered in the contralateral mPFC projections. This finding suggests homeostatic regulation occurs within subcortically but not intracortical callosal-projecting neurons. Increased inhibition of intraprefrontal connectivity may therefore be particularly important for prefrontal cortex circuit maturation. Finally, we observed cognitive deficits in the adult mouse using this narrowed window of thalamocortical inhibition.

青少年丘脑-前额叶抑制导致前额叶内在网络连接发生变化
从出生后第 P20-50 天开始抑制丘脑-皮层投射,会导致成年小鼠前额叶-皮层功能和认知能力的长期缺陷。虽然这表明丘脑活动在前额叶-皮层成熟中的作用,但目前还不清楚抑制这些投射如何影响青春期的前额叶回路。在这里,我们利用化学遗传学工具抑制了P20-35雄性/雌性小鼠的丘脑-前额叶投射,并在24小时后利用切片生理学测量了前额叶锥体神经元各层(II/III或V/VI)和投射目标(MD、NAc或胼胝体mPFC)的突触输入。我们选择了 mPFC 和 MD 投射细胞,因为它们在很大程度上是按皮质层(分别为 II/III 层和 V/VI 层)区分的,而选择 NAc 投射细胞则是因为它们横跨两层,因此为其他两个群体提供了层内比较。我们发现,II/III 层-丘脑核(NAc)和 V/VI 层-丘脑中层投射神经元的兴奋性和抑制性电流频率下降,而 V/VI 层-NAc 投射神经元的兴奋性和抑制性电流振幅增加。在皮层投射方面,对侧 mPFC 投射神经元的抑制性电流频率增加,而兴奋性电流频率则没有增加。值得注意的是,尽管单个兴奋和抑制水平发生了这些复杂的变化,但每个细胞中兴奋和抑制之间的总体平衡只在 mPFC 对侧投射中发生了变化。这一发现表明,皮层下而非皮层内的胼胝体投射神经元会发生平衡调节。因此,增加对前额叶内连接的抑制可能对前额叶-皮层回路的成熟尤为重要。最后,我们利用丘脑皮层抑制的狭窄窗口(P20-P35)观察到了成年小鼠的认知障碍。 重要意义 声明 研究发现,精神分裂症患者丘脑和前额叶皮层这两个脑区之间的连通性降低。丘脑-皮层投射的神经元活动对感觉皮层的正常发育非常重要。至于丘脑皮层活动如何调节前额叶皮层的发育,目前还不太清楚。在这里,我们发现,在青春期早期,小鼠丘脑-前额叶投射活动的减少会改变与前额叶皮质内不同神经元投射的突触连接,而这些神经元投射在青春期已经很明显。其中一些变化可以用丘脑-皮层投射的减少来解释,而另一些适应则是前额叶皮层固有的。这些发现表明,青春期是大脑皮层发育的关键时期,并证明这一时期是治疗干预的潜在目标。
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来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
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