Evidence map›Paper›PMID 40866820›Full record

ArticleBMC gastroenterology2025

Resveratrol mitigates aspirin-induced intestinal injury in rats in a high-altitude hypoxic environment associated with reducing the expression levels of angiotensin II.

Paziliya Abulaiti, Wen Hui Shi, Huan Liu, Ailifeire Tuerxuntayi, Kailibinuer Nuermaimaiti, Zhuo Shuyi Liu, Yingying Xing, Najimangu Rehemutula, Kudelaiti Abdukelimu, Weidong Liu and 2 more

Abstract read
In one paragraph

Article in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Paziliya AbulaitiDepartment of Gastroenterology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
Wen Hui ShiGeneral Hospital of Xinjiang Military Region of PLA, Urumqi, China.
Huan LiuDepartment of Gastroenterology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
Ailifeire TuerxuntayiXinjiang Medical University, Urumqi, China.
Kailibinuer NuermaimaitiXinjiang Medical University, Urumqi, China.
Zhuo Shuyi LiuXinjiang Medical University, Urumqi, China.
Yingying XingShihezi University, Shihezi, China.
Najimangu RehemutulaXinjiang Medical University, Urumqi, China.
Kudelaiti AbdukelimuXinjiang Medical University, Urumqi, China.
Weidong LiuDepartment of Gastroenterology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
Jiang Wei LiuGeneral Hospital of Xinjiang Military Region of PLA, Urumqi, China.
Feng GaoDepartment of Gastroenterology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China. xjgf@sina.com.

Funding

Feng gao 82260116
6 · The paper itself

Abstract

backgroundThis study aimed to investigate whether the polyphenolic compound resveratrol can protect against intestinal injury induced by aspirin in hypoxic rats associated with the inhibition of angiotensin II (Ang-II), as well as mitigating intestinal mucosal oxidative stress and inflammation.

methodThe plain control group rats received daily gavage in a conventional atmosphere, while the high-altitude blank control group rats underwent the same procedure but was housed in a chamber simulating the hypoxic environment in a high-altitude.while the remaining groups rats were also housed in this hypoxic chamber and received daily aspirin gavage to establish an Aspirin-induced intestinal injury model. The resveratrol intervention group was administered resveratrol at varying doses 2 h post-aspirin gavage. Small intestinal mucosal gross morphology and histopathological damage were observed and scored across all groups. ELISA quantified MPO and SOD activity and IL-1β, IL-10, TNF-α levels in intestinal tissues, while immunohistochemistry assessed Ang-II and Intercellular adhesion molecule-1 (ICAM-1) expression.

resultThe high-altitude blank control group rats not only showed substantial intestinal injuries but also exhibited elevated expression of Ang-II and ICAM-1 in the small intestinal tissues of rats, which positively correlated with the degree of histological injury to the mucosa. Furthermore, there was increased expression of pro-inflammatory factors IL-1β and TNF-α, decreased expression of the anti-inflammatory factor IL-10, and elevated levels of the oxidative stress indicator myeloperoxidase (MPO) activity, while the levels of superoxide dismutase (SOD) were decreased in the small intestinal tissues of rats. The administration of aspirin in the hypoxic environment exacerbated intestinal inflammation and damage to the intestinal mucosa. After treatment with Resveratrol intervention, the expression of Ang-II and ICAM-1 was reduced, while oxidative stress and inflammatory responses in the intestinal mucosa were also decreased. The results of HE staining directly demonstrated the damage to the intestines and the repair of the intestinal mucosa after Resveratrol intervention. The effect of medium-dose resveratrol appeared to be particularly pronounced.

conclusionResveratrol can effectively mitigate intestinal injury induced by aspirin at high altitude in hypoxic environments. The mechanism may involve downregulating the expression of Ang-II and ICAM-1, alleviating oxidative stress and the inflammatory response of the intestinal mucosa, and preserving intestinal barrier function.

Indexed as

Angiotensin IIAntioxidantsAspirinHypoxiaIntestinal DiseasesIntestinal MucosaIntestine, SmallResveratrolAltitudeAnimalsDisease Models, AnimalIntercellular Adhesion Molecule-1MaleOxidative StressPeroxidaseRatsAngiotensin IIAntioxidantsAspirinIntercellular Adhesion Molecule-1PeroxidaseResveratrolSuperoxide DismutaseTumor Necrosis Factor-alphaAngiotensin IIAspirinHypoxic environmentIntercellular adhesion molecule-1Resveratrol

Identifiers

PMID40866820
PMCPMC12392596

What OpenQuestion 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 OpenQuestion graph.