Evidence map›Paper›PMID 41221044›Full record

ArticleFrontiers in pharmacology2025

Study on Chaiyuwendan decoction's inhibition of hippocampal neuron apoptosis to alleviating depression by activating the AKT/CREB pathway.

Shaoliang Zhang, Sijie Cheng, Huiqing Liang, Yan Qiu, Jie Ren, Yv Huang, Bangyan Zhou, Chunrong Li, Jingmin Zhang, Tianxiang Wang and 6 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Article
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

16 authors.

Shaoliang ZhangSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Sijie ChengSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Huiqing LiangLiver Disease Center, Xiamen Hospital of Traditional Chinese Medicine, Xiamen, Fujian, China.
Yan QiuSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Jie RenSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Yv HuangSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Bangyan ZhouSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Chunrong LiSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Jingmin ZhangSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Tianxiang WangSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Liuyi WangSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Ruobing LiuSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Qi LiuSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Hongli ZhuangDepartment of Traditional Chinese Medicine, First Affiliated Hospital of Xiamen University, Xiamen, Fujian, China.
Penghua LaiSchool of Medicine, Xiamen University, Xiamen, Fujian, China.
Shaodong ChenSchool of Medicine, Xiamen University, Xiamen, Fujian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hippocampal neuron damage is closely related to depression, and apoptosis is an important pathway for neuronal damage. Depression belongs to Yubing (depressive disease) in traditional Chinese medicine theory. Chaiyuwendan decoction (CYWD) has significant clinical efficacy in treating depression, however, its specific mechanism is still unclear. This study aims to explore the potential pharmacological active substances and key therapeutic targets of CYWD in treating depression from signaling pathways related with apoptosis. Methods: HPLC-MS method was used to detect the key components of CYWD. The mouse depression model was established by CORT injection. Depressive mice were administered CYWD at low, medium and high doses. Behavioral experiment, neurotransmitters in hippocampus and serum, hippocampal HE staining and Nissl staining were tested in order to evaluate the effects of CYWD in antidepressant and anti nerve damage. The potential targets and signaling pathways for CYWD against depression were predicted through network pharmacology and molecular docking. CORT intervention was used to establish a neuronal apoptosis model of HT22. The effect of CYWD on HT22 were evaluated using CCK-8 proliferation, Nissl staining and apoptotic assays by flow cytometry. According to the predicted results, Western blot and Immunofluorescence assay were used to detect AKT, pAKT, CREB, pCREB and apoptosis-related proteins in hippocampus and HT22 cells. Results: 134 active components in CYWD were identified, including chlorogenic acid, coumaric acid, rutinoside, naringin, and hesperidin. The Conclusion: CYWD can alleviate depression through protecting hippocampal neurons by activating the AKT-CREB signaling pathway, increasing the proportion of anti apoptotic proteins. These findings provided a valuable reference to CYWD as a promising alternative against depression.

Indexed as

AKT/CREB signaling pathwayapoptosisChaiyuwendan decoctiondepressionhippocampal neuron

Identifiers

PMID41221044
PMCPMC12598031

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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.