Evidence map›Paper›PMID 26495304›Full record

ArticleBioMed research international2015

Vitamin D can ameliorate chlorhexidine gluconate-induced peritoneal fibrosis and functional deterioration through the inhibition of epithelial-to-mesenchymal transition of mesothelial cells.

Yi-Che Lee, Shih-Yuan Hung, Hung-Hsiang Liou, Tsun-Mei Lin, Chu-Hung Tsai, Sheng-Hsiang Lin, Yau-Sheng Tsai, Min-Yu Chang, Hsi-Hao Wang, Li-Chun Ho and 10 more

Abstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. A Study ofBioMed research international · 2017
    Trial
  2. Article
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  8. Detrimental pro-senescence effects of vitamin D on lung fibrosis.Molecular medicine (Cambridge, Mass.) · 2018
    Article
  9. 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

20 authors.

Yi-Che LeeDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan ; Institute of Clinical Medicine, National Cheng Kung University, Tainan, Taiwan.
Shih-Yuan HungDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan ; School of Medicine for International Students, I-Shou University, Kaohsiung, Taiwan.
Hung-Hsiang LiouDivision of Nephrology, Department of Medicine, Hsin-Jen Hospital, New Taipei City, Taiwan.
Tsun-Mei LinDepartment of Laboratory Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Chu-Hung TsaiInstitute of Clinical Medicine, National Cheng Kung University, Tainan, Taiwan.
Sheng-Hsiang LinInstitute of Clinical Medicine, National Cheng Kung University, Tainan, Taiwan.
Yau-Sheng TsaiInstitute of Clinical Medicine, National Cheng Kung University, Tainan, Taiwan.
Min-Yu ChangDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Hsi-Hao WangDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Li-Chun HoDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan ; Institute of Clinical Medicine, National Cheng Kung University, Tainan, Taiwan.
Yi-Ting ChenDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Ching-Fang WuDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Ho-Ching ChenDivision of Nephrology, Department of Internal Medicine, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Hsin-Pao ChenDivision of Colorectal Surgery, Department of Surgery, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Kuang-Wen LiuDivision of Colorectal Surgery, Department of Surgery, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Chih-I ChenDivision of Colorectal Surgery, Department of Surgery, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Kuan Min SheDivision of Colorectal Surgery, Department of Surgery, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Hao-Kuang WangDepartment of Neurosurgery, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Chi-Wei LinDepartment of Medical Education, I-Shou University, Kaohsiung, Taiwan.
Yuan-Yow ChiouInstitute of Clinical Medicine, National Cheng Kung University, Tainan, Taiwan ; Department of Pediatrics, National Cheng Kung University Hospital, Tainan, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeritoneal dialysis (PD) can induce fibrosis and functional alterations in PD patients' peritoneal membranes, due to long-term unphysiological dialysate exposure, partially occurring via triggering of epithelial-to-mesenchymal transition (EMT) in peritoneal mesothelial cells (MCs). Vitamin D can ameliorate these negative effects; however, the mechanism remains unexplored. Therefore, we investigated its possible links to MCs EMT inhibition.

methodsPeritoneal fibrosis was established in Sprague-Dawley rats by chlorhexidine gluconate (CG) intraperitoneal injection for 21 days, with and without 1α,25(OH)2D3 treatment. Morphological and functional evaluation and western blot analysis of EMT marker were performed upon peritoneum tissue. In vitro study was also performed in a primary human peritoneal MC culture system; MCs were incubated with transforming growth factor-β1 (TGF-β1) in the absence or presence of 1α,25(OH)2D3. EMT marker expression, migration activities, and cytoskeleton redistribution of MCs were determined.

results1α,25(OH)2D3 ameliorated CG-induced morphological and functional deterioration in animal model, along with CG-induced upregulation of α-SMA and downregulation of E-cadherin expression. Meanwhile, 1α,25(OH)2D3 also ameliorated TGF-β1-induced decrease in E-cadherin expression, increase in Snai1 and α-SMA expression, intracellular F-actin redistribution, and migration activity in vitro.

conclusion1α,25(OH)2D3 can ameliorate CG-induced peritoneal fibrosis and attenuate functional deterioration through inhibiting MC EMT.

Indexed as

AnimalsCells, CulturedChlorhexidineDose-Response Relationship, DrugEpithelial-Mesenchymal TransitionEpitheliumHumansMalePeritoneal FibrosisRatsRats, Sprague-DawleyTreatment OutcomeVitamin DChlorhexidinechlorhexidine gluconateVitamin D

Identifiers

PMID26495304
PMCPMC4606086

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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 OpenQuestion graph.