Evidence map›Paper›PMID 35069768›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

Liquiritin Alleviates Depression-Like Behavior in CUMS Mice by Inhibiting Oxidative Stress and NLRP3 Inflammasome in Hippocampus.

Chang Liu, Dai Yuan, Chi Zhang, Ye Tao, Ying Meng, Mengli Jin, Wu Song, Bingmei Wang, Lin Wei

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
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

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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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  3. Neuropsychiatric disease and treatment · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Chang LiuClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.ORCID https://orcid.org/0000-0001-6191-5173
Dai YuanClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.
Chi ZhangSchool of Basic Medicine, Changchun University of Chinese Medicine, Changchun 130117, China.
Ye TaoAffiliated Hospital of Changchun University of Chinese Medicine, Changchun 130021, China.
Ying MengClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.
Mengli JinClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.
Wu SongClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.ORCID https://orcid.org/0000-0002-1314-8018
Bingmei WangClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.ORCID https://orcid.org/0000-0002-8606-8422
Lin WeiClinical Medical College of Changchun University of Chinese Medicine, Changchun 130117, China.ORCID https://orcid.org/0000-0002-2626-8967
Changchun University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCentral inflammation is generally accepted to be involved in the pathology of depression. We investigated whether liquiritin exerts antidepressant effects by inhibiting central NLRP3 inflammasomes.

resultsThe behavioral despair model and chronic unpredictable mild stress (CUMS) model in mice were established to evaluate the antidepressant action of liquiritin. In the despair model study, liquiritin (40 mg/kg) administration reduced immobility time in tail suspension test (TST) and forced swimming test (FST) without affecting locomotion activity. In CUMS model study, liquiritin (40 mg/kg, once daily for 4 weeks) significantly increased sucrose consumption and body weight of CUMS mice. The behavioral experiment results showed that liquiritin reduced the immobile time of CUMS mice in TST and FST, respectively, and increased the time spent and open arm entries in the elevated plus-maze (EPM) test. Further, the hippocampal superoxide dismutase (SOD) activity was increased in liquiritin-treated group, while malonaldehyde (MDA) decreased. Additionally, the hippocampal cytokines interleukin-18 (IL-18) and interleukin-1 beta (IL-1

conclusionsLiquiritin attenuates depression-like behavior of CUMS mice and inhibited cytokines levels triggered by NLRP3 inflammasome, suggesting the antidepressant action is, at least partially, associated with antioxidant stress and inhibition of NLRP3 inflammasome activation.

Identifiers

PMID35069768
PMCPMC8767389
OpenAlexW4205326529

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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.