Evidence map›Paper›PMID 38468130›Full record

ArticleCNS neuroscience & therapeutics2024

Microglial activation in the lateral amygdala promotes anxiety-like behaviors in mice with chronic moderate noise exposure.

Xiaoqi Peng, Yunfeng Mao, Yehao Liu, Qian Dai, Yingju Tai, Bin Luo, Yue Liang, Ruirui Guan, Wenjie Zhou, Lin Chen and 3 more

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
14.0field-weighted citation impact, top 1% of its field
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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Role of the Amygdala in the Complex Relationship Between Sleep and Anxiety.International journal of molecular sciences · 2026
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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

13 authors at 3 institutions in 2 countries.

Xiaoqi PengDepartment of Anesthesiology, The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Yunfeng MaoDepartment of Anesthesiology, The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Yehao LiuSchool of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, China.
Qian DaiSchool of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, China.
Yingju TaiDepartment of Anesthesiology, The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Bin LuoAuditory Research Laboratory, Department of Neurobiology and Biophysics, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Yue LiangDepartment of Otolaryngology, The First Affiliated Hospital of USTC, Hefei, China.
Ruirui GuanDepartment of Otolaryngology, The First Affiliated Hospital of USTC, Hefei, China.
Wenjie ZhouSongjiang Research Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Lin ChenAuditory Research Laboratory, Department of Neurobiology and Biophysics, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.ORCID 0000-0002-5847-2989
Zhi ZhangDepartment of Anesthesiology, The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.ORCID 0000-0002-4205-3181
Guoming ShenSchool of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, China.ORCID 0000-0002-5983-0370
Haitao WangSchool of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, China.
University of Science and Technology of China · CNAnhui University of Traditional Chinese Medicine · CNShanghai Jiao Tong University · CN

Funding

CAS Project for Young Scientists in Basic Research YSBR-013National Key Research and Development Program of China STI2030-Major Projects 2021ZD0203100National Natural Science Foundation of China 32025017National Natural Science Foundation of China 32121002Natural Science Foundation of Anhui Province 2208085MC56Natural Science Research of Anhui Provincial Education Department 2022AH040075Plans for Major Provincial Science&Technology Projects 202303a07020002Shanghai Natural Science Foundation 23ZR1480900
6 · The paper itself

Abstract

backgroundLong-term non-traumatic noise exposure, such as heavy traffic noise, can elicit emotional disorders in humans. However, the underlying neural substrate is still poorly understood.

methodsWe exposed mice to moderate white noise for 28 days to induce anxiety-like behaviors, measured by open-field, elevated plus maze, and light-dark box tests. In vivo multi-electrode recordings in awake mice were used to examine neuronal activity. Chemogenetics were used to silence specific brain regions. Viral tracing, immunofluorescence, and confocal imaging were applied to define the neural circuit and characterize the morphology of microglia.

resultsExposure to moderate noise for 28 days at an 85-dB sound pressure level resulted in anxiety-like behaviors in open-field, elevated plus maze, and light-dark box tests. Viral tracing revealed that fibers projecting from the auditory cortex and auditory thalamus terminate in the lateral amygdala (LA). A noise-induced increase in spontaneous firing rates of the LA and blockade of noise-evoked anxiety-like behaviors by chemogenetic inhibition of LA glutamatergic neurons together confirmed that the LA plays a critical role in noise-induced anxiety. Noise-exposed animals were more vulnerable to anxiety induced by acute noise stressors than control mice. In addition to these behavioral abnormalities, ionized calcium-binding adaptor molecule 1 (Iba-1)-positive microglia in the LA underwent corresponding morphological modifications, including reduced process length and branching and increased soma size following noise exposure. Treatment with minocycline to suppress microglia inhibited noise-associated changes in microglial morphology, neuronal electrophysiological activity, and behavioral changes. Furthermore, microglia-mediated synaptic phagocytosis favored inhibitory synapses, which can cause an imbalance between excitation and inhibition, leading to anxiety-like behaviors.

conclusionsOur study identifies LA microglial activation as a critical mediator of noise-induced anxiety-like behaviors, leading to neuronal and behavioral changes through selective synapse phagocytosis. Our results highlight the pivotal but previously unrecognized roles of LA microglia in chronic moderate noise-induced behavioral changes.

Indexed as

AnxietyMicrogliaAmygdalaAnimalsHumansMiceNeuronsSynapsesanxiety-like behaviorschronic moderate noise exposureelectrophysiologylateral amygdalamicroglia

Identifiers

PMID38468130
PMCPMC10927919
OpenAlexW4392712787

What OpenQuestion holds

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LicenceCC BY
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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.