Evidence map›Paper›PMID 33199803›Full record

ArticleScientific reports2020

Intravenous administration of sodium propionate induces antidepressant or prodepressant effect in a dose dependent manner.

Chunyan Hao, Zefeng Gao, XianJun Liu, Zhijiang Rong, Jingjing Jia, Kaiqi Kang, Weiwei Guo, Jianguo Li

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 31% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

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  15. Dietary Factors Impact Developmental Trajectories in Young Autistic Children.Journal of autism and developmental disorders · 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

8 authors at 2 institutions in 1 country.

Chunyan HaoSchool of Chemical and Biological Engineering, Taiyuan University of Science & Technology, Taiyuan, 030021, China.
Zefeng GaoKey Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institutes of Biomedical Sciences, Shanxi University, No. 92, Wucheng Road, Xiaodian District, TaiyuanShanxi, 030006, China.
XianJun LiuSchool of Chemical and Biological Engineering, Taiyuan University of Science & Technology, Taiyuan, 030021, China.
Zhijiang RongSchool of Chemical and Biological Engineering, Taiyuan University of Science & Technology, Taiyuan, 030021, China.
Jingjing JiaSchool of Life Science, Shanxi University, Taiyuan, 030006, China.
Kaiqi KangSchool of Life Science, Shanxi University, Taiyuan, 030006, China.
Weiwei GuoSchool of Life Science, Shanxi University, Taiyuan, 030006, China.
Jianguo LiKey Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institutes of Biomedical Sciences, Shanxi University, No. 92, Wucheng Road, Xiaodian District, TaiyuanShanxi, 030006, China. lijg@sxu.edu.cn.
Shanxi University · CNTaiyuan University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Propionate has been reported to exert antidepressant effects, but high-dose propionate may induce autism-like symptoms in experimental animals through induction of dysbiosis of neurotransmitters. The bi-directional effects of propionate seem to be dose-dependent. However, due to the pathological discrepancies between depression and autism, conclusions drawn from autism may not be simply transferable to depression. The effect and underlying action mechanisms of high-dose propionate on depression remains undetermined. To investigate the effects of propionate on depression, propionate dose gradients were intravenously administrated to rats exposed to chronic unpredictable mild stress (CUMS) for 1 week. Results of these behavioral tests demonstrate that low-dose propionate (2 mg/kg body weight/day) induces antidepressant effect through bodyweight recovery, elevated reward-seeking behaviors, and reduced depression-like behaviors, while high-dose propionate (200 mg/kg body weight/day) induces prodepressant effects opposite of those of low-dose propionate. A comprehensive profiling of neurotransmitters in the hippocampus demonstrated that CUMS induces reduction of NE (Norepinephrine), DA (Dopamine). GABA (γ-aminobutyric acid) was recovered by low-dose propionate, while high-dose propionate exerted more complicated effects on neurotransmitters, including reduction of NE, DA, 5-Hydroxytryptamine and Tryptophan, and increase of GABA, Kynurenine, Homovanillic acid, 3-hydroxyanthranilic acid, 3-hydroxykynurenine, 3,4-dihydroxyphenylacetic acid, and 3-methoxytyramine. The neurotransmitters disturbed by high-dose propionate suggest metabolic disorders in the hippocampus, which were confirmed by the clear group separation in PCA of metabolomic profiling. The results of this study demonstrate the double-edged dose-dependent effects of propionate on depression and suggest potential cumulative toxicity of propionate as a food additive to mood disorders.

Indexed as

Behavior, AnimalDisease Models, AnimalAdministration, IntravenousAnimalsAntidepressive AgentsDepressionDose-Response Relationship, DrugMalePropionatesRatsRats, Sprague-DawleyStress, PsychologicalAntidepressive AgentsPropionatessodium propionate

Identifiers

PMID33199803
PMCPMC7670463
OpenAlexW3098529305

What OpenQuestion holds

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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.