Evidence mapPaperPMID 42365576Full record

ArticleMolecular biomedicine2026

5-methoxytryptamine improves hepatic inflammation and insulin resistance in a macrophage C-X-C motif chemokine ligand 14 dependent manner.

Xiaoyu Liao, Yuxi Xiao, Bingyao Liu, Yuan Dong, Hang Yang, Linlin Zhang, Dong Li, Peiye Sun, Yixiang Feng, Ying Yang and 4 more

Abstract read
In one paragraph

Article in Molecular biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xiaoyu Liao *Department of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China. liaoxiaoyu2010@163.com.
Yuxi Xiao *Department of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Bingyao Liu *Department of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Yuan Dong *Department of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Hang Yang *Department of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Linlin ZhangDepartment of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Dong LiDepartment of Endocrinology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China.
Peiye SunDepartment of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Yixiang FengDepartment of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Ying YangDepartment of Clinical Laboratory Medicine, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Liqun ZhangDepartment of Clinical Laboratory Medicine, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Qingwu YangDepartment of Neurology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Qiang TongDepartment of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
Hongting ZhengDepartment of Endocrinology, Metabolic and Chronic Disease Science Innovation Center, Translational Research of Diabetes Key Laboratory of Chongqing, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China. fnf7703@hotmail.com.ORCID http://orcid.org/0000-0002-6930-0103

Funding

Chongqing Medical Talent Project No. YXGD202578Chongqing Xinqiao Hospital, Second Affiliated Hospital of Army Medical University No. 2022YQB057Natural Science Foundation of Chongqing No. CSTB2025NSCQ-GPX0655Science and Technology Research Program of Chongqing Municipal Education Commission No. KJQN202512813the National Natural Science Foundation of China No. 82230025the National Natural Science Foundation of China No. 82370815the National Natural Science Foundation of China No. U24A20673
6 · The paper itself

Abstract

Accumulating evidence indicates that tryptophan metabolism plays important roles in insulin resistance, and glucolipid metabolism. Our preliminary study revealed a significant decrease in the serum levels of the tryptophan metabolite 5-methoxytryptamine (5MT), in both high-fat diet (HFD)-fed and db/db mice. Notably, these levels were restored following treatment with the hypoglycemic agent, the dipeptidyl peptidase-4 inhibitor (DPP-4i) sitagliptin, suggesting a potential relationship between 5MT and metabolic homeostasis. In the current study, we demonstrated that 5MT treatment ameliorated insulin resistance and hepatic steatosis in HFD and db/db mice. Specific inhibition of the aryl hydrocarbon receptor (AHR) attenuated the beneficial effects of 5MT on insulin resistance in HFD mice. Transcriptome sequencing and subsequent validation revealed that 5MT significantly upregulated the expression of C-X-C motif chemokine ligand 14 (Cxcl14) in hepatic macrophages. Myeloid-specific knockout of Cxcl14 demonstrated that 5MT inhibited hepatic inflammatory response to improve insulin resistance in a macrophage CXCL14-dependent manner. Furthermore, molecular mechanism exploration revealed that 5MT promoted the AHR-mediated transcriptional activation of Cxcl14, which inhibited glycolysis in macrophages, subsequently suppressing their proinflammatory classical activation (M1 phenotype). Collectively, these data reveal a novel beneficial role of 5MT in insulin resistance and metabolic homeostasis, providing a rationale for new therapeutic strategies targeting insulin resistance-associated metabolic disorders, such as obesity and diabetes.

Indexed as

Chemokines, CXCInflammationInsulin ResistanceLiverMacrophagesAnimalsDiet, High-FatFatty LiverMaleMiceMice, Inbred C57BLReceptors, Aryl HydrocarbonChemokines, CXCReceptors, Aryl Hydrocarbon5-methoxytryptamineCXCL14InflammationInsulin resistanceMacrophages

Identifiers

PMID42365576
PMCPMC13310876

What Socratic 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 Socratic graph.