Perirhinal cortex gains control of hippocampal seizures via broad downstream circuits in male mouse models

The perirhinal cortex (PRh) has extensive interconnections with limbic structures, including the fasciola cinerea (FC), a recently identified node and therapeutic target in temporal lobe epilepsy. However, the neural circuit basis between PRh and FC in seizure progression remains unclear. Here we show that the PRh provides the principal excitatory input to the FC and plays an important role in seizure modulation in male mouse epilepsy models. PRh-FC projections are strongly activated during seizures, and their inhibition delays seizure progression. Moreover, PRh excitatory neurons bidirectionally regulate seizure development and engage multiple distinct downstream pathways, including projections to the FC, infralimbic cortex, and lateral entorhinal cortex. Notably, suppressing PRh activity produces more effective seizure attenuation than targeting individual projections. These findings identify the PRh as a critical hub that coordinates distributed circuits to control seizure progression, highlighting its potential as a therapeutic target for epilepsy treatment.

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Publication Details

Journal
Nature Communications
Published
2026-04-17
DOI
https://doi.org/10.1038/s41467-026-71913-y
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Perirhinal cortex gains control of hippocampal seizures via broad downstream circuits in male mouse models

Nanxi Lai, Z Y Chen, Yuhao Sun, Zhisheng Li et al.
Nature Communications
Neuroscience and Neuropharmacology Research
article

Perirhinal cortex gains control of hippocampal seizures via broad downstream circuits in male mouse models

Nanxi Lai, Z Y Chen, Yuhao Sun, Zhisheng Li, Wangjialu Lu, Yuying Shao, Jing Xi, Fan Fei, Heming Cheng, Jialu Chen
article en

Abstract

The perirhinal cortex (PRh) has extensive interconnections with limbic structures, including the fasciola cinerea (FC), a recently identified node and therapeutic target in temporal lobe epilepsy. However, the neural circuit basis between PRh and FC in seizure progression remains unclear. Here we show that the PRh provides the principal excitatory input to the FC and plays an important role in seizure modulation in male mouse epilepsy models. PRh-FC projections are strongly activated during seizures, and their inhibition delays seizure progression. Moreover, PRh excitatory neurons bidirectionally regulate seizure development and engage multiple distinct downstream pathways, including projections to the FC, infralimbic cortex, and lateral entorhinal cortex. Notably, suppressing PRh activity produces more effective seizure attenuation than targeting individual projections. These findings identify the PRh as a critical hub that coordinates distributed circuits to control seizure progression, highlighting its potential as a therapeutic target for epilepsy treatment.

Nature Communications
Zhejiang Chinese Medical University (CN), Ministry of Education (NZ)
National Natural Science Foundation of China, Natural Science Foundation of Zhejiang Province
Good health and well-being
Openalex Percentile: Top 12%
Neuroscience and Neuropharmacology Research
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