Evidence map›Paper›PMID 32333225›Full record

ArticleAMB Express2020

Therapeutic effect of GLP-1 engineered strain on mice model of Alzheimer's disease and Parkinson's disease.

Xin Fang, Xiaoting Zhou, Yuqing Miao, Yiwen Han, Jing Wei, Tingtao Chen

Open access · goldAbstract read
In one paragraph

Article in AMB Express, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Neuroprotection of engineeredJournal of Zhejiang University. Science. B · 2026
    Article
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  9. Gut: The gate and key to brain.Chinese medical journal · 2025
    Review
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  13. Article
  14. Aqueous Extract ofFoods (Basel, Switzerland) · 2024
    Article
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  19. Brain sciences · 2024
    Article
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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

6 authors at 1 institution in 1 country.

Xin FangDepartment of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Xiaoting ZhouDepartment of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yuqing MiaoNational Engineering Research Center for Bioengineering Drugs and the Technologies, Institute of Translational Medicine, Nanchang University, 1299 Xuefu Road, Honggu District, Nanchang, 330031, Jiangxi, People's Republic of China.
Yiwen HanNational Engineering Research Center for Bioengineering Drugs and the Technologies, Institute of Translational Medicine, Nanchang University, 1299 Xuefu Road, Honggu District, Nanchang, 330031, Jiangxi, People's Republic of China.
Jing WeiNational Engineering Research Center for Bioengineering Drugs and the Technologies, Institute of Translational Medicine, Nanchang University, 1299 Xuefu Road, Honggu District, Nanchang, 330031, Jiangxi, People's Republic of China.
Tingtao ChenDepartment of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China. chentingtao1984@163.com.ORCID http://orcid.org/0000-0002-0506-8536
Nanchang University · CN

Funding

Excellent Youth Foundation of Jiangxi Scientific Committee 20171BCB23028National Natural Science Foundation of China 81660203
6 · The paper itself

Abstract

Alzheimer's disease (AD) and Parkinson's disease (PD) are neurodegenerative diseases (NDD) characterized by progressive degeneration of the central nervous system, and few medications are available to halt the progression of AD and PD. In the present study, an engineered strain MG136-pMG36e-GLP-1 was used to evaluate its neuroprotective effect on AD and PD mice, via the probiotics effects of Lactococcus lactis MG1363 and the constantly produced Glucagon-like peptide-1 (GLP-1) by the engineered strain. Our results indicated that oral administration of MG136-pMG36e-GLP-1 significantly reduced lipopolysaccharide (LPS)-induced memory impairment and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced motor dysfunction through the toll-like receptor4 (TLR4)/nuclear factor-kappa B (NFκB) and protein kinase B (AKT)/Glycogen synthase kinase-3β (GSK3β) signaling pathway. High-throughput sequencing results showed that MG1363-pMG36e-GLP-1 reduced the abundance of the pathogens Enterococcus, Proteus, and increased the abundance of the probiotics Akkermansia muciniphila. These results suggest that the engineered strain may be a new intervention for treating AD and PD by reducing the occurrence of neuroinflammation.

Indexed as

Alzheimer’s disease (AD)Engineered bacteriaGlucagon-like peptide-1 (GLP-1)High-throughput sequencingMG1363-pMG36e-GLP-1NeuroinflammationParkinson’s disease (PD)

Identifiers

PMID32333225
PMCPMC7182653
OpenAlexW3018058123

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.