Evidence map›Paper›PMID 31762213›Full record

ArticleJournal of cellular and molecular medicine2020

Proteomics-based screening of the target proteins associated with antidepressant-like effect and mechanism of Saikosaponin A.

Juanjuan Guo, Feng Zhang, Jifang Gao, Xinyuan Guan, Beiyun Liu, Xiaoge Wang, Zhaoyu Qin, Kuanxiao Tang, Shilian Liu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 51 citations in OpenAlex.

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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

9 authors at 7 institutions in 1 country.

Juanjuan GuoDepartment of Biochemistry and Molecular Biology, School of Medicine, Shandong University, Jinan, China.
Feng ZhangSchool of Life Sciences, Qilu Normal University, Jinan, China.
Jifang GaoDepartment of Pathology, Linyi People's Hospital, Linyi, China.
Xinyuan GuanBureau of Emergency Management of Siping City, Siping, China.
Beiyun LiuShanghai United Imaging Healthcare Co., Ltd., Shanghai, China.
Xiaoge WangGuangzhou Hospital of integrated Traditional and West Medicine, Guangzhou, China.
Zhaoyu QinLaboratory of Systems Biology, Institute of Biomedical Sciences, Fudan University, Shanghai, China.
Kuanxiao TangDepartment of Geriatrics, Qilu Hospital of Shandong Univeristy, Jinan, China.
Shilian LiuDepartment of Biochemistry and Molecular Biology, School of Medicine, Shandong University, Jinan, China.ORCID 0000-0002-2881-8918
Shandong University · CNFudan University · CNIntegrated Chinese Medicine (China) · CNLinyi People's Hospital · CNQilu Hospital of Shandong University · CNQilu Normal University · CNUnited Imaging Healthcare (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression is a commonly occurring neuropsychiatric disease with an increasing incidence rate. Saikosaponin A (SA), a major bioactive component extracted from Radix Bupleuri, possesses anti-malignant cell proliferation, anti-inflammation, anti-oxidation and liver protective effects. However, few studies have investigated SA's antidepressant effects and pharmacological mechanisms of action. Our study aimed to explore the anti-depression effect of SA and screen the target proteins regulated by SA in a rat model of chronic unpredictable mild stress (CUMS)-induced depression. Results showed that 8-week CUMS combined with separation could successfully produce depressive-like behaviours and cause a decrease of dopamine (DA) in rat hippocampus, and 4-week administration of SA could relieve CUMS rats' depressive symptoms and up-regulated DA content. There were 15 kinds of significant differentially expressed proteins that were detected not only between the control and CUMS groups, but also between the CUMS and SA treatment groups. Proline-rich transmembrane protein 2 (PRRT2) was down-regulated by CUMS while up-regulated by SA. These findings reveal that SA may exert antidepressant effects by up-regulating the expression level of PRRT2 and increasing DA content in hippocampus. The identification of these 15 differentially expressed proteins, including PRRT2, provides further insight into the treatment mechanism of SA for depression.

Indexed as

Disease Models, AnimalAnimalsAntidepressive AgentsAnti-Inflammatory Agents, Non-SteroidalDepressive DisorderDopamineMaleOleanolic AcidProteomeRatsRats, Sprague-DawleySaponinsStress, PsychologicalAntidepressive AgentsAnti-Inflammatory Agents, Non-SteroidalDopamineOleanolic AcidProteomesaikosaponin DSaponinsdepressiondopamineproline-rich transmembrane protein 2proteomicsSaikosaponin A

Identifiers

PMID31762213
PMCPMC6933357
OpenAlexW2990086160

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.