Evidence map›Paper›PMID 40624321›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2025

Distinct subpopulations of parvalbumin neurons participating in divergent prefrontal functions.

Yehong Hu, Xinyang Zhang, Tsz Hei Fong, Tianyu Wang, Jin Zhang, Yujie Zhang, Qiang Zhou

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Parvalbumin interneurons under stress: converging mechanisms of vulnerability.The international journal of neuropsychopharmacology · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Yehong HuSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China.ORCID http://orcid.org/0009-0009-1907-5583
Xinyang ZhangSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China.
Tsz Hei FongSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China.
Tianyu WangSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China.
Jin ZhangSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China.
Yujie ZhangPediatric Neurology, Shenzhen Children's Hospital, Shenzhen, China.
Qiang ZhouSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China. zhouqiang@pkusz.edu.cn.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82204356
6 · The paper itself

Abstract

Prefrontal parvalbumin (PV) neurons play crucial roles in various distinct functions, while malfunction of PV-neurons also has critical contributions to various brain diseases, including both psychiatric and neurodegenerative disorders. However, whether the prefrontal cortex (PFC) PV-neurons participating in these functions and malfunctions are distinct subpopulations is not well understood. This question is important for a better understanding of both the basic properties/function of PV-neurons and inhibitory neurons in general, and for potential comorbid occurrence of dysfunctions in disease settings. Here, we analyzed dorsomedial prefrontal cortex (dmPFC) PV-neurons participating in working memory, modulation of conditioned fear memory, and anxiety, regarding their relative localization, electrophysiological properties, and synaptic inputs. In addition, by using activity-dependent tagging method, we examined whether manipulating the dmPFC PV-neurons participating in one function may affect another function as a way to test for potential functional interactions between them. We found that: (1) one single group of dmPFC PV-neurons participating in the two forms of modulation of conditioned fear memory, based on their high overlap in localization and mutual functional interactions with each other. (2) dmPFC PV-neurons participating in fear memory modulation and anxiety are two different subpopulations, with unique electrophysiological properties. (3) dmPFC PV-neurons participating in working memory and fear memory modulation are two different subpopulations, with different synaptic and neuronal properties. These findings provide important insights into the organization of PV-neurons in the PFC and highlight the distinct and non-interacting nature of different PV-subpopulations in the PFC functional diversity.

Indexed as

Memory, Short-TermNeuronsParvalbuminsPrefrontal CortexAnimalsAnxietyFearMaleMiceMice, Inbred C57BLMice, TransgenicParvalbumins

Identifiers

PMID40624321
PMCPMC12340019

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.