Evidence map›Paper›PMID 41104239›Full record

ArticleIranian journal of pharmaceutical research : IJPR

Schisanhenol Alleviates Mycophenolic Acid-Induced Intestinal Epithelial Cell Barrier Damage by Activating the Nrf2/HO-1 Signaling Pathway.

Yiyun Deng, Jiawang Fan, Chunlan Yang, Yan Huang, Qingrong Xia, Jun Liang, Dujuan Xu, Yan Du, Yong Su

Abstract read
In one paragraph

Article in Iranian journal of pharmaceutical research : IJPR. 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

9 authors.

Yiyun DengDepartment of Pharmacy, Affiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Jiawang FanSchool of Pharmacy, Anhui Medical University, Hefei, China.
Chunlan YangDepartment of Pharmacy, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Yan HuangDepartment of Pharmacy, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Qingrong XiaDepartment of Pharmacy, Affiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Jun LiangDepartment of Pharmacy, Affiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Dujuan XuDepartment of Pharmacy, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Yan DuDepartment of Pharmacy, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Yong SuSchool of Pharmacy, Anhui Medical University, Hefei, China.ORCID https://orcid.org/0000-0002-2655-1412

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Reactive oxygen species (ROS)-mediated apoptosis of intestinal epithelial cells and tight junction (TJ) protein loss play critical roles in mycophenolic acid (MPA)-induced disruption of intestinal epithelial barrier function, yet no effective therapeutic strategies exist. Schisanhenol (Sal), a major component of the traditional Chinese medicine Wuzhi capsule, exhibits strong antioxidant activity. Objectives: The present study aimed to investigate the protective efficacy and mechanisms of Sal against MPA-induced damage to the intestinal mechanical barrier. Methods: Caco-2 cells were exposed to MPA (10 μM), Sal (5, 10, and 25 μM), or ML385 (2 μM) for 24 hours. Cell viability was measured via a Cell Counting Kit-8 (CCK-8) assay. The expression of apoptosis-related and TJ proteins was evaluated through Western blot analysis. Flow cytometry was used to quantify the percentage of apoptotic Caco-2 cells. Immunofluorescence assays were performed to assess the localization of TJ proteins. Intracellular ROS levels were measured using H2DCFDA staining. Oxidative and antioxidative biomarker levels were quantified using specific assay kits. Results: Sal significantly increased the viability of MPA-treated cells. It also upregulated Bcl-2 expression and reduced apoptosis. Furthermore, Sal increased the expression of the TJ proteins ZO-1 and occludin. Additionally, Sal upregulated the MPA-mediated decrease in Nrf2/HO-1 expression, reduced intracellular ROS accumulation, and increased the levels of antioxidants, including SOD, CAT, and GSH. However, ML385 partially abrogated the protective effects of Sal. Conclusions: Schisanhenol alleviates MPA-induced intestinal mechanical barrier damage via modulation of the Nrf2 signaling pathway, highlighting its antioxidant and antiapoptotic properties.

Indexed as

AntioxidantMycophenolic AcidReactive Oxygen SpeciesSchisanhenolTight Junctions

Identifiers

PMID41104239
PMCPMC12523734

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.