Evidence map›Paper›PMID 38383920›Full record

ArticleMolecular neurobiology2024

Neuron-Microglia Interaction is Involved in Anti-inflammatory Response by Vagus Nerve Stimulation in the Prefrontal Cortex of Rats Injected with Polyinosinic:Polycytidylic Acid.

Ki-Joong Kim, Jinyeon Hwang, Kang-Woo Lee, Jieun Kim, Yunha Han, Uk Namgung

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
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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

6 authors at 1 institution in 1 country.

Ki-Joong KimDepartment of Korean Medicine, Institute of Bioscience and Integrative Medicine, Daejeon University, Daehak‑ro 62, Daejeon, 34520, South Korea.
Jinyeon HwangDepartment of Korean Medicine, Institute of Bioscience and Integrative Medicine, Daejeon University, Daehak‑ro 62, Daejeon, 34520, South Korea.
Kang-Woo LeeDepartment of Korean Medicine, Institute of Bioscience and Integrative Medicine, Daejeon University, Daehak‑ro 62, Daejeon, 34520, South Korea.
Jieun KimDepartment of Korean Medicine, Institute of Bioscience and Integrative Medicine, Daejeon University, Daehak‑ro 62, Daejeon, 34520, South Korea.
Yunha HanDepartment of Korean Medicine, Institute of Bioscience and Integrative Medicine, Daejeon University, Daehak‑ro 62, Daejeon, 34520, South Korea.
Uk NamgungDepartment of Korean Medicine, Institute of Bioscience and Integrative Medicine, Daejeon University, Daehak‑ro 62, Daejeon, 34520, South Korea. unamgung@dju.kr.ORCID http://orcid.org/0000-0001-5253-1143
Daejeon University · KR

Funding

Daejeon University 20220159National Research Foundation of Korea NRF-2018R1A6A1A03025221
6 · The paper itself

Abstract

Injection of polyinosinic:polycytidylic acid (poly(I:C)) into experimental animals induces neuroimmunological responses and thus has been used for the study of neurological disorders such as anxiety, depression, and chronic fatigue. Here, we investigated the effects of vagus nerve stimulation (VNS) on poly(I:C)-induced neuroinflammation and associated behavioral consequences in rats. The microglia in the prefrontal cortex (PFC) displayed the activated form of morphology in poly(I:C)-injected rats and changed to a normal shape after acute VNS (aVNS). Production of phospho-NF-κB, phospho-IκB, IL-1β, and cleaved caspase 3 was elevated by poly(I:C) and downregulated by aVNS. In contrast, phospho-Akt levels were decreased by poly(I:C) and increased by aVNS. Neuronal production of fractalkine (CX3CL1) in the PFC was markedly reduced by poly(I:C), but recovered by aVNS. Fractalkine interaction with its receptor CX3CR1 was highly elevated by VNS. We further demonstrated that the pharmacological blockade of CX3CR1 activity counteracted the production of IL-1β, phospho-Akt, and cleaved form of caspase 3 that was modulated by VNS, suggesting the anti-inflammatory effects of fractalkine-CX3CR1 signaling as a mediator of neuron-microglia interaction. Behavioral assessments of pain and temperature sensations by von Frey and hot/cold plate tests showed significant improvement by chronic VNS (cVNS) and forced swimming and marble burying tests revealed that the depressive-like behaviors caused by poly(I:C) injection were rescued by cVNS. We also found that the recognition memory which was impaired by poly(I:C) administration was improved by cVNS. This study suggests that VNS may play a role in regulating neuroinflammation and somatosensory and cognitive functions in poly(I:C)-injected animals.

Indexed as

Chemokine CX3CL1MicrogliaNeuronsPoly I-CPrefrontal CortexRats, Sprague-DawleyVagus Nerve StimulationAnimalsBehavior, AnimalCell CommunicationCX3C Chemokine Receptor 1InflammationInterleukin-1betaMaleProto-Oncogene Proteins c-aktRatsChemokine CX3CL1CX3C Chemokine Receptor 1Interleukin-1betaPoly I-CProto-Oncogene Proteins c-aktNeuroinflammationPolyinosinic:polycytidylic acidPrefrontal cortexVagus nerve stimulation

Identifiers

PMID38383920
OpenAlexW4392057196

What OpenQuestion holds

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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.