Evidence map›Paper›PMID 35626632›Full record

ArticleCells2022

P-Coumaric Acid Reverses Depression-Like Behavior and Memory Deficit Via Inhibiting AGE-RAGE-Mediated Neuroinflammation.

Xu-Dong Yu, Dan Zhang, Chu-Li Xiao, Yu Zhou, Xing Li, Le Wang, Zhiming He, James Reilly, Zhi-Yong Xiao, Xinhua Shu

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 48 citations in OpenAlex.

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  18. Beneficial Effects ofNutrients · 2024
    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

10 authors at 3 institutions in 2 countries.

Xu-Dong YuDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
Dan ZhangDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
Chu-Li XiaoDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
Yu ZhouDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
Xing LiDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
Le WangDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
Zhiming HeDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.
James ReillyDepartment of Biological and Biomedical Sciences, Glasgow Caledonian University, Glasgow G4 0BA, UK.
Zhi-Yong XiaoThe First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang 421001, China.
Xinhua ShuDepartment of Physiology, School of Basic Medical Sciences, Shaoyang University, Shaoyang 422000, China.ORCID 0000-0003-3760-3019
Shaoyang University · CNGlasgow Caledonian University · GBUniversity of South China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression, a mood disorder, affects one in fifteen adults, has multiple risk factors and is associated with complicated underlying pathological mechanisms. P-coumaric acid (p-CA), a phenolic acid, is widely distributed in vegetables, fruits and mushrooms. P-CA has demonstrated a protective role against oxidative stress and inflammation in various diseases, including cardiovascular disease, diabetes and cancer. In the current study, we investigated the protection of p-CA against depression and memory impairment in a corticosterone (CORT)-induced chronic depressive mouse model. CORT administration resulted in depression-like behaviors and memory impairment. P-CA treatment alleviated CORT-induced depression-related behaviors and memory impairment. Network pharmacology predicted that p-CA had multiple targets and mediated various signaling pathways, of which inflammation-associated targets and signaling pathways are predominant. Western blotting showed CORT-induced activation of the advanced glycation end product (AGE)-receptor of AGE (RAGE) (AGE-RAGE) signaling and increased expression of the proinflammatory cytokines interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNFα) in the hippocampus, while p-CA treatment inactivated AGE-RAGE signaling and decreased the levels of IL-1β and TNFα, suggesting that protection against depression and memory impairment by p-CA is mediated by the inhibition of inflammation, mainly via the AGE-RAGE signaling pathway. Our data suggest that p-CA treatment will benefit patients with depression.

Indexed as

Glycation End Products, AdvancedTumor Necrosis Factor-alphaAnimalsCoumaric AcidsDepressionHumansInflammationMemory DisordersMiceNeuroinflammatory DiseasesReceptor for Advanced Glycation End ProductsAger protein, mouseCoumaric AcidsGlycation End Products, Advancedp-coumaric acidReceptor for Advanced Glycation End ProductsTumor Necrosis Factor-alphaAGE-RAGE signaling pathwaydepressioninflammationnetwork pharmacologyp-coumaric acid

Identifiers

PMID35626632
PMCPMC9139330
OpenAlexW4280529950

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.