Functional properties of corticothalamic circuits targeting paraventricular thalamic neurons.

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-11-02 DOI:10.1016/j.neuron.2024.10.010
Guillermo Aquino-Miranda, Dounya Jalloul, Xu O Zhang, Sa Li, Gilbert J Kirouac, Michael Beierlein, Fabricio H Do Monte
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Abstract

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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以丘脑室旁神经元为目标的皮质-丘脑回路的功能特性
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。
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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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