Evidence map›Paper›PMID 35848938›Full record

ArticleBrain and behavior2022

Ginsenoside Rh2 administration produces crucial antidepressant-like effects in a CUMS-induced mice model of depression.

Lin-Sheng Shi, Chun-Hui Ji, Yue Liu, Jiang-Hong Gu, Wen-Qian Tang, Wei Zhang, Wei Guan

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  7. Frontiers in molecular biosciences · 2025
    Article
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  9. GluN2A: A Promising Target for Developing Novel Antidepressants.The international journal of neuropsychopharmacology · 2024
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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

7 authors at 1 institution in 1 country.

Lin-Sheng ShiDepartment of Cardiology, Affiliated Hospital 2 of Nantong University, Nantong, China.
Chun-Hui JiDepartment of Pharmacology, Pharmacy College, Nantong University, Nantong, China.
Yue LiuDepartment of Pharmacology, Pharmacy College, Nantong University, Nantong, China.
Jiang-Hong GuDepartment of Pharmacology, Pharmacy College, Nantong University, Nantong, China.
Wen-Qian TangDepartment of Pharmacology, Pharmacy College, Nantong University, Nantong, China.
Wei ZhangDepartment of Pharmacology, Pharmacy College, Nantong University, Nantong, China.
Wei GuanDepartment of Pharmacology, Pharmacy College, Nantong University, Nantong, China.ORCID 0000-0002-7967-3456
Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe most striking feature of depression is sadness and a loss of interest in activities, which represents a major cause of disability globally. Therefore, it is necessary to identify novel antidepressants for clinical practice. Ginsenoside Rh2 (Rh2) is one of the major bioactive ginsenosides that can be extracted from Panax ginseng and has been demonstrated to improve both memory and learning. The purpose of this study was to provide broad insight into the mechanisms underlying depression and gain greater insights into antidepressant therapy.

methodsIn this study, we first established an effective and feasible depression animal model of chronic unpredictable mild stress (CUMS) and behavioral testing was evaluated by the forced swim test (FST), the tail suspension test (TST) and the sucrose preference test. Following pretreatment with Rh2 (10 and 20 mg/kg), the immobility time of mice was reduced without affecting locomotor activity in both the FST and TST. Western blotting and immunofluorescence were used to investigate the activation of the hippocampal BDNF signaling pathway and hippocampal neurogenesis.

resultsDifferent concentrations of Rh2 significantly reduced depressive-like symptoms in CUMS-induced mice and downregulated the effects of the BDNF signaling cascade and neurogenesis in the hippocampus. Furthermore, the administration of K252a completely prevented the antidepressant-like activity of Rh2 in mice.

conclusionThe results indicated that Rh2 possesses the antidepression action via the positive regulation of the BDNF-TrkB pathway.

Indexed as

GinsenosidesAnimalsAntidepressive AgentsBrain-Derived Neurotrophic FactorDepressionDisease Models, AnimalHippocampusMiceStress, PsychologicalAntidepressive AgentsBrain-Derived Neurotrophic Factorginsenoside Rh2Ginsenosidesbrain-derived neurotrophic factorchronic unpredictable mild stressdepressionginsenoside Rh2

Identifiers

PMID35848938
PMCPMC9392527
OpenAlexW4285727289

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.