Evidence map›Paper›PMID 30816479›Full record

ArticleMolecular medicine reports2019

Curcumin and resveratrol suppress dextran sulfate sodium‑induced colitis in mice.

Lize Zhang, Hui Xue, Gang Zhao, Cuixia Qiao, Xiaomei Sun, Chengjian Pang, Dianliang Zhang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Pooled it
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  5. mCellular and molecular life sciences : CMLS · 2025
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  12. Smooth Muscle Silent Information Regulator 1 Contributes to Colitis in Mice.International journal of molecular sciences · 2025
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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 2 institutions in 1 country.

Lize ZhangDepartment of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Hui XueDepartment of Gynecology, Qingdao Hospital of Traditional Chinese Medicine, Qingdao, Shandong 266000, P.R. China.
Gang ZhaoDepartment of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Cuixia QiaoDepartment of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Xiaomei SunDepartment of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Chengjian PangDepartment of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Dianliang ZhangCenter of Colon and Rectum, Qingdao Municipal Hospital, Qingdao, Shandong 266011, P.R. China.
Affiliated Hospital of Qingdao University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Curcumin and resveratrol are two natural products, which have been described as potential anti‑inflammatory, anti‑tumor, and anti‑oxidant molecules. The aims of the present study were to investigate the protective effect of curcumin and resveratrol on dextran sulfate sodium (DSS)‑induced ulcerative colitis (UC) in mice, in addition to understanding the underlying molecular mechanisms. In order to accomplish this, BALB/c mice received drinking water containing 3.5% DSS. Curcumin (50 mg/kg/day) or resveratrol (80 mg/kg/day) were administered orally for 7 days. Survival rate, body weight, disease activity index score, colon length, pro‑inflammatory cytokines, and the expression autophagy‑associated proteins, and mechanistic target of rapamycin (mTOR) and sirtuin 1 (SIRT1) were measured. Curcumin or resveratrol treatment prolonged the survival of mice with UC, reduced body weight loss and attenuated the severity of the disease compared with the DSS‑treated mice. This effect was associated with a substantial clinical amelioration of the disruption of the colonic architecture and a significant reduction in pro‑inflammatory cytokine production. Furthermore, curcumin or resveratrol significantly downregulated the expression of autophagy‑related 12, Beclin‑1 and microtubule‑associated protein light chain 3 II, and upregulated the expression of phosphorylated mTOR and SIRT1 in the colon tissue, compared with those in the DSS‑treated group. These results suggest that curcumin and resveratrol exert protective effects on DSS‑induced UC, partially through suppressing the intestinal inflammatory cascade reaction, reducing autophagy and regulating SIRT1/mTOR signaling.

Indexed as

AnimalsAnti-Inflammatory AgentsBiopsyColitisCurcuminCytokinesDextran SulfateDisease Models, AnimalFluorescent Antibody TechniqueInflammation MediatorsIntestinal MucosaMaleMiceResveratrolSirtuin 1TOR Serine-Threonine KinasesAnti-Inflammatory AgentsCurcuminCytokinesDextran SulfateInflammation MediatorsResveratrolSirtuin 1TOR Serine-Threonine Kinases

Identifiers

PMID30816479
PMCPMC6423642
OpenAlexW2915995611

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.