Evidence map›Paper›PMID 40085651›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

The reuniens thalamus recruits recurrent excitation in the medial prefrontal cortex.

Gil Vantomme, Gabrielle Devienne, Jacob M Hull, John R Huguenard

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Gil VantommeDepartment of Neurology and Neurological Sciences, Stanford University, Stanford, CA 94304.ORCID 0000-0002-7441-0737
Gabrielle DevienneDepartment of Neurology and Neurological Sciences, Stanford University, Stanford, CA 94304.ORCID 0000-0002-2204-8043
Jacob M HullDepartment of Neurology and Neurological Sciences, Stanford University, Stanford, CA 94304.
John R HuguenardDepartment of Neurology and Neurological Sciences, Stanford University, Stanford, CA 94304.ORCID 0000-0002-6950-1191

Funding

Inhibitory Controls of Thalamic NeuronsR01NS034774 · NINDS · STANFORD UNIVERSITY · PI HUGUENARD, JOHN R · 1996 to 2021
$5.5M
Inhibitory Controls in the Thalamic Reticular NucleusR37NS034774 · NINDS · STANFORD UNIVERSITY · PI HUGUENARD, JOHN R · 2004 to 2010
$2.5M
Tracking pre-seizure dynamics to predict and control seizuresR01NS117150 · NINDS · STANFORD UNIVERSITY · PI GANGULI, SURYA, HUGUENARD, JOHN R · 2020 to 2024
$2.1M
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS34774NINDS NIH HHS R01 NS034774NINDS NIH HHS R01 NS117150NINDS NIH HHS R37 NS034774Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) P2LAP3-199556
6 · The paper itself

Abstract

The medial prefrontal cortex (mPFC) and hippocampus are critical for memory retrieval, decision making, and emotional regulation. While ventral CA1 (vCA1) shows direct and reciprocal connections with mPFC, dorsal CA1 (dCA1) forms indirect pathways to mPFC, notably via the thalamic reuniens nucleus (Re). Neuroanatomical tracing has documented structural connectivity of this indirect pathway through Re however, its functional operation is largely unexplored. Here, we used in vivo and in vitro electrophysiology along with optogenetics to address this question. Whole-cell patch-clamp recordings in acute mouse brain slices revealed both monosynaptic excitatory responses and disynaptic feedforward inhibition at Re-mPFC synapses. However, we also identified a prolonged excitation of mPFC by Re. These early monosynaptic and late recurrent components are in marked contrast to the primarily feedforward inhibition characteristic of thalamic inputs to the neocortex. Local field potential recordings in mPFC brain slices revealed prolonged synaptic activity throughout all cortical lamina upon Re activation, with the late excitation enhanced by blockade of parvalbumin neurons and GABA

Indexed as

Midline Thalamic NucleiPrefrontal CortexAnimalsCA1 Region, HippocampalMaleMiceMice, Inbred C57BLNeural PathwaysNeuronsOptogeneticsPatch-Clamp TechniquesSynapseselectrophysiologyhippocampusprefrontal cortexreuniens

Identifiers

PMID40085651
PMCPMC11929439

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.