Evidence map›Paper›PMID 36926728›Full record

ArticleNeural regeneration research2023

Inhibiting 5-hydroxytryptamine receptor 3 alleviates pathological changes of a mouse model of Alzheimer's disease.

Li-Fen Liu, Yu-Tong Liu, Dan-Dan Wu, Jie Cheng, Na-Na Li, Ya-Ni Zheng, Liang Huang, Qiong-Lan Yuan

Open access · goldAbstract read
In one paragraph

Article in Neural regeneration research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Serotonergic Regulation in Alzheimer's Disease.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Article
  9. Phytoconstituents Targeting the Serotonin 5-HTACS pharmacology & translational science · 2024
    Review
  10. Neural regeneration research · 2024
    Article
  11. Article
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 3 institutions in 2 countries.

Li-Fen LiuDepartment of Neurology, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Yu-Tong LiuDepartment of Radiology, University of Nebraska Medical Center, Omaha, NE, USA.
Dan-Dan WuDepartment of Neurology, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Jie ChengDepartment of Neurology, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Na-Na LiDepartment of Neurology, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Ya-Ni ZhengDepartment of Neurology, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Liang HuangDepartment of Neurology, Shanghai Tongji Hospital; Department of Human Anatomy, Histology & Embryology, Tongji University School of Medicine, Shanghai, China.
Qiong-Lan YuanDepartment of Neurology, Shanghai Tongji Hospital; Department of Human Anatomy, Histology & Embryology, Tongji University School of Medicine, Shanghai, China.
Tongji University · CNTongji Hospital · CNUniversity of Nebraska Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular amyloid beta (Aβ) plaques are main pathological feature of Alzheimer's disease. However, the specific type of neurons that produce Aβ peptides in the initial stage of Alzheimer's disease are unknown. In this study, we found that 5-hydroxytryptamin receptor 3A subunit (HTR3A) was highly expressed in the brain tissue of transgenic amyloid precursor protein and presenilin-1 mice (an Alzheimer's disease model) and patients with Alzheimer's disease. To investigate whether HTR3A-positive interneurons are associated with the production of Aβ plaques, we performed double immunostaining and found that HTR3A-positive interneurons were clustered around Aβ plaques in the mouse model. Some amyloid precursor protein-positive or β-site amyloid precursor protein cleaving enzyme-1-positive neurites near Aβ plaques were co-localized with HTR3A interneurons. These results suggest that HTR3A -positive interneurons may partially contribute to the generation of Aβ peptides. We treated 5.0-5.5-month-old model mice with tropisetron, a HTR3 antagonist, for 8 consecutive weeks. We found that the cognitive deficit of mice was partially reversed, Aβ plaques and neuroinflammation were remarkably reduced, the expression of HTR3 was remarkably decreased and the calcineurin/nuclear factor of activated T-cell 4 signaling pathway was inhibited in treated model mice. These findings suggest that HTR3A interneurons partly contribute to generation of Aβ peptide at the initial stage of Alzheimer's disease and inhibiting HTR3 partly reverses the pathological changes of Alzheimer's disease.

Indexed as

5-hydroxytryptamin receptor 3Alzheimer’s diseaseamyloid beta plaquescalcineurincognitive deficitsHTR3 interneuronsiCa2+nuclear factor of activated T-cellstransgenic amyloid precursor protein and presenilin-1 micetropisetron

Identifiers

PMID36926728
PMCPMC10233771
OpenAlexW4321124041

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.