Evidence map›Paper›PMID 40065319›Full record

ArticleJournal of nanobiotechnology2025

Ginseng exosomes modulate M1/M2 polarisation by activating autophagy and target IKK/IкB/NF-кB to alleviate inflammatory bowel disease.

Song Yang, Liangliang Fan, Lijia Yin, Yueming Zhao, Wenjing Li, Ronghua Zhao, Xuxia Jia, Fusong Dong, Ze Zheng, Daqing Zhao and 1 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Advances in Research onInternational journal of molecular sciences · 2026
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  5. [EstradiolZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
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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

11 authors.

Song YangChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Liangliang FanChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Lijia YinChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Yueming ZhaoChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Wenjing LiChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Ronghua ZhaoChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Xuxia JiaChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Fusong DongChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Ze ZhengChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Daqing ZhaoChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China.
Jiawen WangChangchun University of Chinese Medicine, 1035 Boshuo Road, Changchun, 130117, Jilin Province, China. wangjiawen1229@163.com.

Funding

Jilin Provincial Postdoctoral Science Foundation 0103011103
6 · The paper itself

Abstract

backgroundExosomes are involved in intercellular communication and regulation of the inflammatory microenvironment. In a previous study, we demonstrated that fresh ginseng exosomes (GEs) alleviated inflammatory bowel disease. However, the precise mechanism by which GEs activate the immune system and subsequently inhibit the formation of intestinal inflammatory microenvironment remains unknown.

methodsHerein, we investigated the effects of GEs on autophagy, macrophage polarisation, intestinal inflammation, and the epithelial barrier by means of transcriptome sequencing, network pharmacology, transmission electron microscopy, immunoblotting, flow cytometry and small molecule inhibitors.

resultsGEs significantly activated autophagy and M2-like macrophage polarisation, which could be blocked by the autophagy inhibitor 3-methyladenine. In the co-culture system of macrophages and intestinal epithelial cells, macrophages treated with GEs secreted more interleukin-10 (IL-10) and significantly reduced Nitric oxide (NO) levels in intestinal epithelial cells in vitro. Furthermore, GEs acted directly on intestinal epithelial cells through the IKK/IкB/NF-кB signalling pathway to reduce inflammation and restore the intestinal barrier. Orally administered GEs could restore disrupted colonic barriers, alleviate inflammatory bowel responses, and regulate the polarisation of intestinal macrophages in vivo.

conclusionIn summary, GEs may be a potential treatment for inflammatory bowel disease, and targeting autophagy and macrophage polarisation may help alleviate intestinal inflammation.

Indexed as

AutophagyExosomesInflammatory Bowel DiseasesPanaxAnimalsEpithelial CellsHumansI-kappa B KinaseInterleukin-10MacrophagesMaleMiceMice, Inbred C57BLNF-kappa BRAW 264.7 CellsSignal TransductionI-kappa B KinaseInterleukin-10NF-kappa BAutophagyGinseng exosomesIntestinal barrierM1/M2 polarisation

Identifiers

PMID40065319
PMCPMC11895377

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.