Evidence map›Paper›PMID 33298623›Full record

ArticleAging2020

Liraglutide improved the cognitive function of diabetic mice via the receptor of advanced glycation end products down-regulation.

Haoqiang Zhang, Yafen Chu, Hongwei Zheng, Jing Wang, Bing Song, Yao Sun

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In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

15 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

6 authors at 4 institutions in 1 country.

Haoqiang ZhangDepartment of Endocrinology, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Yafen ChuDepartment of Endocrinology, Ningbo Medical Center Lihuili Hospital, Ningbo, China.
Hongwei ZhengDepartment of Endocrinology, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Jing WangDepartment of Endocrinology, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Bing SongDepartment of Endocrinology, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Yao SunDepartment of Pharmacy, Taikang Xianlin Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Jinzhou Medical University · CNNanjing Drum Tower Hospital · CNNingbo Medical Center Lihuili Hospital · CNZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims Advanced glycation end products (AGEs) and receptor of advanced glycation end products (RAGE), are associated with cognition decline. We aim to investigate the effect of liraglutide on cognitive function in diabetic mice. Results Diabetic mice showed decreased cognitive function. Moreover, lower glucagon like peptide-1 (GLP-1) levels in plasma were detected in db/db mice. Additionally, up-regulated RAGE and down-regulated glucagon like peptide-1 (GLP-1R) levels were observed in db/db mice. However, decreased GLP-1R and increased RAGE were reversed by liraglutide. We also found decreased cellular activity in cells with AGEs. Moreover, AGEs up-regulated RAGE in PC12 and HT22 cells. However, liraglutide improved the cell activity damaged by AGEs. Although we did not discover the direct-interaction between RAGE and GLP-1R, elevated RAGE levels induced by AGEs were restored by liraglutide. Conclusion We demonstrated that the cognitive function of diabetic mice was improved by liraglutide via the down-regulation of RAGE. Methods db/db mice and db/m mice were used in this study. Liraglutide was used to remedy diabetic mice. Neurons and RAGE in hippocampus were shown by immunofluorescence. And then, PC12 cells or HT22 cells with AGEs were treated with liraglutide. GLP-1R and RAGE were measured by western blotting.

Indexed as

AnimalsCell SurvivalCognitionCognitive DysfunctionDiabetes MellitusGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorGlycation End Products, AdvancedHippocampusHypoglycemic AgentsLiraglutideMiceMice, ObeseNeuronsPC12 CellsRatsAger protein, mouseGlp1r protein, mouseGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorGlycation End Products, AdvancedHypoglycemic AgentsLiraglutideReceptor for Advanced Glycation End Productscognitive functiondiabetes mellitusliraglutidereceptor of advanced glycation end products

Identifiers

PMID33298623
PMCPMC7835012
OpenAlexW3108481511

What Socratic holds

Textfull text, public
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 Socratic graph.