Evidence map›Paper›PMID 25379005›Full record

ArticleJournal of ginseng research2014

Korean Red Ginseng attenuates anxiety-like behavior during ethanol withdrawal in rats.

ZhengLin Zhao, Young Woo Kim, YiYan Wu, Jie Zhang, Ju-Hee Lee, XiaoHua Li, Il Je Cho, Sang Mi Park, Dae Hwa Jung, Chae Ha Yang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 22 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

12 authors at 2 institutions in 2 countries.

ZhengLin ZhaoDepartment of Pharmacology, Mudanjiang Medical University, Mudanjiang, China ; Medical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
Young Woo KimMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
YiYan WuDepartment of Pharmacology, Mudanjiang Medical University, Mudanjiang, China.
Jie ZhangDepartment of Pharmacology, Mudanjiang Medical University, Mudanjiang, China.
Ju-Hee LeeMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
XiaoHua LiDepartment of Pharmacology, Mudanjiang Medical University, Mudanjiang, China.
Il Je ChoMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
Sang Mi ParkMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
Dae Hwa JungMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
Chae Ha YangMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
Sang Chan KimMedical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
RongJie ZhaoDepartment of Pharmacology, Mudanjiang Medical University, Mudanjiang, China ; Medical Research Center, College of Oriental Medicine, Daegu Haany University, Daegu, Korea.
Daegu Haany University · KRMudanjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKorean Red Ginseng (KRG) is known to have antianxiety properties. This study was conducted to investigate the anxiolytic effects of KRG extract (KRGE) during ethanol withdrawal (EW) and the involvement of the mesoamygdaloid dopamine (DA) system in it.

methodsRats were treated with 3 g/kg/d of ethanol for 28 d, and subjected to 3 d of withdrawal. During EW, KRGE (20 mg/kg/d or 60 mg/kg/d, p.o.) was given to rats once/d for 3 d. Thirty min after the final dose of KRGE, anxiety-like behavior was evaluated in an elevated plus maze (EPM), and plasma corticosterone (CORT) levels were determined by a radioimmunoassay (RIA). In addition, concentrations of DA and 3,4-dihydroxyphenylacetic acid (DOPAC) in the central nucleus of the amygdala (CeA) were also measured by high performance liquid chromatography (HPLC).

resultsThe EPM test and RIA revealed KRGE inhibited anxiety-like behavior and the over secretion of plasma CORT during EW. Furthermore, the behavioral effect was blocked by a selective DA D2 receptor (D2R) antagonist (eticlopride) but not by a selective DA D1 receptor (D1R) antagonist (SCH23390). HPLC analyses showed KRGE reversed EW-induced decreases of DA and DOPAC in a dose-dependent way. Additionally, Western blotting and real-time polymerase chain reaction (PCR) assays showed that KRGE prevented the EW-induced reductions in tyrosine hydroxylase (TH) protein expression in the CeA and TH mRNA expression in the ventral tegmental area (VTA).

conclusionThese results suggest that KRGE has anxiolytic effects during EW by improving the mesoamygdaloid DA system.

Indexed as

amygdalaanxietydopamineethanol withdrawalPanax ginseng

Identifiers

PMID25379005
PMCPMC4213848
OpenAlexW2103315882

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.