Evidence map›Paper›PMID 39334486›Full record

ArticleJournal of neuroinflammation2024

Tryptophan-rich diet and its effects on Htr7

Dinghao Xue, Xu Guo, Jingjing Liu, Yanxiang Li, Luyu Liu, Guosong Liao, Mingru Zhang, Jiangbei Cao, Yanhong Liu, Jingsheng Lou and 4 more

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
  4. Review
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  6. Article
  7. Review
  8. Article
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  11. Article
  12. 5-HTCNS neuroscience & therapeutics · 2025
    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

14 authors.

Dinghao Xue *Department of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Xu Guo *Department of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Jingjing Liu *Department of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Yanxiang LiDepartment of Anesthesiology, The 71st Group Army Hospital of CPLA Army, Xuzhou, 221004, China.
Luyu LiuDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Guosong LiaoDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Mingru ZhangDepartment of Anesthesiology, Beijing Tongren Hospital, Capital Medical University, Beijing, 100730, China.
Jiangbei CaoDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Yanhong LiuDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Jingsheng LouDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Hao LiDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Weidong MiDepartment of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China.
Long Wang *Department of Pain Medicine, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China. flynn.xu@163.com.
Qiang Fu *Department of Anesthesiology, The First Medical Center, Chinese PLA General Hospital, Beijing, 100853, China. dr_fuqiang@hotmail.com.

Funding

National Natural Science Foundation of China 82071178National Natural Science Foundation of China 82271322
6 · The paper itself

Abstract

backgroundNeuroinflammation is a vital pathogenic mechanism for neurodegenerative diseases such as Alzheimer's, schizophrenia, and age-related cognitive decline. Regulatory T cells (Tregs) exhibit potent anti-inflammatory properties and can modulate neurodegenerative diseases arising from central nervous system inflammatory responses. However, the role of Tregs in neuroinflammation-related cognitive dysfunction remains unclear. It is highly plausible that Htr7

methodsMice were given a tryptophan-rich diet (with a tryptophan content of 0.6%) or a normal diet (with a tryptophan content of 0.16%). The neuroinflammation-mediated cognitive dysfunction model was established by intracerebroventricular injection of lipopolysaccharide (LPS) in 8-week-old C57BL/6J mice. The activation and infiltration of Tregs were measured using flow cytometry. Primary Tregs were cocultured separately with primary CD8

resultsIn this study, the tryptophan-rich diet was found to reverse LPS-induced cognitive impairment and reduce the levels of 5-HT in peripheral blood. The tryptophan-rich diet led to increased levels of 5-HT in peripheral blood, which in turn promoted the proliferation and activation of Htr7

conclusionsOur research revealed the ability of Htr7

Indexed as

Cognitive DysfunctionLipopolysaccharidesMice, Inbred C57BLNeuroinflammatory DiseasesReceptors, SerotoninT-Lymphocytes, RegulatoryTryptophanAnimalsDietMaleMiceMice, KnockoutLipopolysaccharidesReceptors, Serotoninserotonin 7 receptorTryptophanCognitive dysfunctionLipopolysaccharideNeuroinflammationRegulatory T cellsSerotonin

Identifiers

PMID39334486
PMCPMC11437714

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Registered trials

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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.