Evidence map›Paper›PMID 38075046›Full record

ReviewFrontiers in endocrinology2023

Bile acid signalling and its role in anxiety disorders.

Simin Chen, Qi Shao, Jiayi Chen, Xinyi Lv, Jing Ji, Yan Liu, Yuehan Song

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 17 citations in OpenAlex.

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  12. Emerging Roles of Bile Acids in Neuroinflammation.International journal of molecular sciences · 2025
    Review
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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

7 authors at 1 institution in 1 country.

Simin ChenCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Qi ShaoCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Jiayi ChenCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Xinyi LvCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Jing JiCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Yan LiuCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Yuehan SongCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anxiety disorder is a prevalent neuropsychiatric disorder that afflicts 7.3%~28.0% of the world's population. Bile acids are synthesized by hepatocytes and modulate metabolism via farnesoid X receptor (FXR), G protein-coupled receptor (TGR5), etc. These effects are not limited to the gastrointestinal tract but also extend to tissues and organs such as the brain, where they regulate emotional centers and nerves. A rise in serum bile acid levels can promote the interaction between central FXR and TGR5 across the blood-brain barrier or activate intestinal FXR and TGR5 to release fibroblast growth factor 19 (FGF19) and glucagon-like peptide-1 (GLP-1), respectively, which in turn, transmit signals to the brain via these indirect pathways. This review aimed to summarize advancements in the metabolism of bile acids and the physiological functions of their receptors in various tissues, with a specific focus on their regulatory roles in brain function. The contribution of bile acids to anxiety via sending signals to the brain via direct or indirect pathways was also discussed. Different bile acid ligands trigger distinct bile acid signaling cascades, producing diverse downstream effects, and these pathways may be involved in anxiety regulation. Future investigations from the perspective of bile acids are anticipated to lead to novel mechanistic insights and potential therapeutic targets for anxiety disorders.

Indexed as

Receptors, G-Protein-CoupledSignal TransductionAnxiety DisordersBile Acids and SaltsHumansIntestinesBile Acids and SaltsReceptors, G-Protein-Coupledanxiety disordersbile acid signalingFGF19FXRGLP-1TGR5

Identifiers

PMID38075046
PMCPMC10710157
OpenAlexW4388964266

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.