Evidence map›Paper›PMID 38444330›Full record

ArticleBrain and behavior2024

Dulaglutide treatment reverses depression-like behavior and hippocampal metabolomic homeostasis in mice exposed to chronic mild stress.

Man Jin, Shipan Zhang, Boya Huang, Litao Li, Hao Liang, Aihua Ni, Lina Han, Peng Liang, Jing Liu, Haishui Shi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Contractile effects of dulaglutide in the human atrium.Naunyn-Schmiedeberg's archives of pharmacology · 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

11 authors at 2 institutions in 1 country.

Man JinDepartment of Neurology, Hebei Medical University, Shijiazhuang, China.ORCID 0009-0003-4140-7261
Shipan ZhangDepartment of Neurology, Hebei Medical University, Shijiazhuang, China.
Boya HuangNeuroscience Research Center, Institute of Medical and Health Science, Hebei Medical University, Shijiazhuang, China.
Litao LiDepartment of Neurology, Hebei Medical University, Shijiazhuang, China.
Hao LiangHebei Provincial Key Laboratory of Cerebral Networks and Cognitive Disorders, Shijiazhuang, China.
Aihua NiDepartment of Neurology, Hebei General Hospital, Shijiazhuang, China.
Lina HanDepartment of Neurology, Hebei General Hospital, Shijiazhuang, China.
Peng LiangDepartment of Neurology, Hebei Medical University, Shijiazhuang, China.
Jing LiuDepartment of Neurology, Hebei Medical University, Shijiazhuang, China.
Haishui ShiNursing School, Hebei Medical University, Shijiazhuang, China.
Peiyuan LvDepartment of Neurology, Hebei Medical University, Shijiazhuang, China.
Hebei Medical University · CNHebei University of Economics and Business · CN

Funding

Hebei Natural Science Foundation H2022307075Hebei Provincial Medical Science Research Project 20220821Hebei Provincial Medical Science Research Project 20241259
6 · The paper itself

Abstract

introductionTreatment strategies for depression based on interventions for glucose and lipid metabolism disorders are receiving increasing attention. Investigating the mechanism of their antidepressant effect and exploring new diagnostic and therapeutic biomarkers have attracted increasing attention. Dulaglutide, a long-acting GLP-1 receptor agonist, has been reported to alleviate cognitive deficits and neuronal damage. However, the antidepressant effect of dulaglutide and, especially, the underlying mechanism are still poorly understood. In this study, we aimed to explore the underlying biomarkers of depression and potential modulatory targets of dulaglutide in chronic mild stress (CMS) mice.

methodsSixty mice were randomly divided into a control group (CON group), a CMS+Vehicle group (CMS+Veh group), a CMS+0.3 mg/kg dulaglutide group (Low Dula group), and a CMS+0.6 mg/kg dulaglutide group (High Dula group). Numerous behavioral tests, mainly the open field test, forced swimming test, and tail suspension test, were applied to evaluate the potential effect of dulaglutide treatment on anxiety- and depression-like behaviors in mice exposed to chronic stress. Furthermore, a liquid chromatography-tandem mass spectrometry-based metabolomics approach was utilized to investigate the associated mechanisms of dulaglutide treatment.

resultsThree weeks of dulaglutide treatment significantly reversed depressive-like but not anxiety-like behaviors in mice exposed to chronic stress for 4 weeks. The results from the metabolomics analysis showed that a total of 20 differentially expressed metabolites were identified between the CON and CMS+Veh groups, and 46 metabolites were selected between the CMS+Veh and High Dula groups in the hippocampus of the mice. Comprehensive analysis indicated that lipid metabolism, amino acid metabolism, energy metabolism, and tryptophan metabolism were disrupted in model mice that experienced depression and underwent dulaglutide therapy.

conclusionThe antidepressant effects of dulaglutide in a CMS depression model were confirmed. We identified 64 different metabolites and four major pathways associated with metabolic pathophysiological processes. These primary data provide a new perspective for understanding the antidepressant-like effects of dulaglutide and may facilitate the use of dulaglutide as a potential therapeutic strategy for depression.

Indexed as

Antidepressive AgentsDepressionImmunoglobulin Fc FragmentsRecombinant Fusion ProteinsAnimalsBiomarkersGlucagon-Like PeptidesHomeostasisMiceAntidepressive AgentsBiomarkersdulaglutideGlucagon-Like PeptidesImmunoglobulin Fc FragmentsRecombinant Fusion Proteinsdepressiondulaglutideliquid chromatography-tandem mass spectrometrymetabolomics

Identifiers

PMID38444330
PMCPMC10915471
OpenAlexW4392516423

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.