Evidence map›Paper›PMID 33461175›Full record

ArticleAging2021

Intranasal treatment of lixisenatide attenuated emotional and olfactory symptoms via CREB-mediated adult neurogenesis in mouse depression model.

Guoyong Ren, Pan Xue, Bin Wu, Fei Yang, Xuemei Wu

Open access · greenAbstract read
In one paragraph

Article in Aging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Olfactory Dysfunction in Mental Illness.Current allergy and asthma reports · 2023
    Review
  10. Article
  11. Review
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

5 authors at 2 institutions in 1 country.

Guoyong RenDepartment of Neurology, General Hospital of TISCO, Sixth Hospital of Shanxi Medical University, Taiyuan, China.
Pan XueDepartment of Neurology, General Hospital of TISCO, Sixth Hospital of Shanxi Medical University, Taiyuan, China.
Bin WuDepartment of Neurology, General Hospital of TISCO, Sixth Hospital of Shanxi Medical University, Taiyuan, China.
Fei YangDepartment of Neurology, General Hospital of TISCO, Sixth Hospital of Shanxi Medical University, Taiyuan, China.
Xuemei WuDepartment of Neurology, General Hospital of TISCO, Sixth Hospital of Shanxi Medical University, Taiyuan, China.
Taiyuan Iron and Steel Group (China) · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Convergent lines of evidence indicate a striking correlation between olfactory deficits and depressive symptoms. However, the effectiveness of intranasal treatment of antidepressant or other neurotrophic agents remains poorly understanding. Here in this study, we created depression mouse model and explored the antidepressant effects of GLP-1 analog lixisenatide (LXT) with intranasal treatment. Consecutive intranasal treatment of LXT remarkably reduced the depressive and anxiety behaviors. Meanwhile, it also improved the olfactory memory and olfactory sensitivity. Immunofluorescent analysis demonstrated the LXT improved the adult neurogenesis in olfactory system and hippocampus. Inhibition of adult neurogenesis with TMZ caused the compromised effects of LXT in improving emotional and olfactory functions, suggesting the vital role of adult neurogenesis in LXT induced depression therapeutic effects. Treatment of LXT resulted in the increased phosphorylation of CREB protein in hippocampal tissue, indicating CREB plays important roles in antidepressant effects of LXT intranasal treatment. Inhibiting CREB with chemical approach decreased effects of LXT in reserving depression induced emotional and olfactory functions. In conclusion, our study suggests intranasal treatment of LXT could be a potential antidepressant to improve the olfactory functions as well as the emotional behaviors.

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsAdministration, IntranasalAnimalsBehavior, AnimalCyclic AMP Response Element-Binding ProteinDepressionDepressive DisorderDisease Models, AnimalElevated Plus Maze TestGlucagon-Like Peptide-2 ReceptorHindlimb SuspensionHippocampusMiceNeurogenesisOlfaction DisordersOlfactory BulbCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinGlucagon-Like Peptide-1 Receptor AgonistsGlucagon-Like Peptide-2 ReceptorlixisenatidePeptidesCREBdepressionlixisenatideneurogenesisolfactory function

Identifiers

PMID33461175
PMCPMC7906191
OpenAlexW3120407910

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.