Evidence map›Paper›PMID 39619328›Full record

ReviewFrontiers in endocrinology2024

The potential mechanism of action of gut flora and bile acids through the TGR5/TRPV1 signaling pathway in diabetic peripheral neuropathic pain.

Peng Chen, Xian Jiang, Jia Fu, Cehua Ou, Yao Li, Jing Jia, Changli Liao

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

9 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Gut microbiota-mediated pain sensitization: mechanisms and therapeutic implications.Frontiers in pain research (Lausanne, Switzerland) · 2025
    Review
  8. Review
  9. 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

7 authors.

Peng Chen *Department of Pediatrics, Southwest Medical University, Luzhou, Sichuan, China.
Xian Jiang *Department of Anesthesiology, Luzhou People's Hospital, Luzhou, Sichuan, China.
Jia FuDepartment of Pain Management, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan, China.
Cehua OuDepartment of Pain Management, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan, China.
Yao LiDepartment of Science and Technology, Southwest Medical University, Luzhou, Sichuan, China.
Jing JiaDepartment of Anesthesiology, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan, China.
Changli LiaoDepartment of Science and Technology, Southwest Medical University, Luzhou, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic peripheral neuropathic pain (DPNP) is a major complication of diabetes that markedly affects the quality of life and health status of patients. Recent studies have investigated the potential regulatory influence of gut flora and bile acids on DPNP via the TGR5/TRPV1 signaling pathway. Dysbiosis of the gut flora not only directly affects bile acid metabolism but also significantly correlates with diabetes-associated neuropathy through interactions with the bile acid receptor TGR5 and the ion channel TRPV1. This review describes how alterations in the gut flora and bile acid metabolism contribute to the pathogenesis of DPNP through the TGR5/TRPV1 signaling pathway, revealing potential applications for this pathway in DPNP management. Furthermore, experimental and clinical studies have demonstrated the modulation of gut flora and bile acid metabolism as well as targeting the TGR5/TRPV1 signaling pathway as an innovative therapeutic approach. Further studies are warranted to elucidate the underlying mechanism and develop treatment modalities based on gut flora regulation and signaling pathway interventions, thus providing novel insights and approaches for DPNP therapy.

Indexed as

Bile Acids and SaltsDiabetic NeuropathiesGastrointestinal MicrobiomeReceptors, G-Protein-CoupledSignal TransductionTRPV Cation ChannelsAnimalsHumansBile Acids and SaltsGPBAR1 protein, humanReceptors, G-Protein-CoupledTRPV1 protein, humanTRPV Cation Channelsbile acidsdiabetic peripheral neuropathic paingut floraTGR5TRPV1

Identifiers

PMID39619328
PMCPMC11604420

What OpenQuestion holds

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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.