以丘脑室旁神经元为目标的皮质-丘脑回路的功能特性

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Guillermo Aquino-Miranda, Dounya Jalloul, Xu O Zhang, Sa Li, Gilbert J Kirouac, Michael Beierlein, Fabricio H Do Monte
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引用次数: 0

摘要

皮质-丘脑向丘脑感觉运动核的投射显示出适度的发射率,并起到调节丘脑中继神经元活动的作用。相比之下,我们在这里发现,从边缘前皮层(PL)到丘脑前室旁核(aPVT)的高阶皮质-丘脑投射保持着高频率的活动,并唤起大鼠 aPVT 神经元的强烈突触兴奋。在很大一部分 aPVT 细胞中,PL-aPVT 投射的这种高频兴奋导致动作电位振幅快速衰减,随后出现去极化阻滞(DB),强烈限制了 aPVT 的最大发射率,从而以频率依赖性方式调节防御和食欲行为。丘脑网状核(avTRN)前腹部的强抑制性输入在高棘波保真度期间抑制了 aPVT 神经元的发射率,但在突出的 DB 期间恢复了发射率,这表明 avTRN 的活动可以调节 PL 输入对 aPVT 发射率的影响,从而最终控制动机行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional properties of corticothalamic circuits targeting paraventricular thalamic neurons.

Corticothalamic projections to sensorimotor thalamic nuclei show modest firing rates and serve to modulate the activity of thalamic relay neurons. By contrast, here we find that high-order corticothalamic projections from the prelimbic (PL) cortex to the anterior paraventricular thalamic nucleus (aPVT) maintain high-frequency activity and evoke strong synaptic excitation of aPVT neurons in rats. In a significant fraction of aPVT cells, such high-frequency excitation of PL-aPVT projections leads to a rapid decay of action potential amplitudes, followed by a depolarization block (DB) that strongly limits aPVT maximum firing rates, thereby regulating both defensive and appetitive behaviors in a frequency-dependent manner. Strong inhibitory inputs from the anteroventral portion of the thalamic reticular nucleus (avTRN) inhibit the firing rate of aPVT neurons during periods of high-spike fidelity but restore it during prominent DB, suggesting that avTRN activity can modulate the effects of PL inputs on aPVT firing rates to ultimately control motivated behaviors.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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