Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis

Peritoneal dialysis (PD) serves as a home-based kidney replacement therapy with increasing utilization across the globe. However, long-term use of high-glucose-based PD solution incites repeated peritoneal injury and inevitable peritoneal fibrosis, thus compromising treatment efficacy and resulting...

Full description

Saved in:
Bibliographic Details
Main Authors: Yu-Wei Chen, Mei-Yi Wu, Nai-Jen Huang, Mai-Szu Wu, Yung-Ho Hsu, Chia-Te Liao, Cheng-Hsien Chen
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Marine Drugs
Subjects:
Online Access:https://www.mdpi.com/1660-3397/22/12/529
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850036807630061568
author Yu-Wei Chen
Mei-Yi Wu
Nai-Jen Huang
Mai-Szu Wu
Yung-Ho Hsu
Chia-Te Liao
Cheng-Hsien Chen
author_facet Yu-Wei Chen
Mei-Yi Wu
Nai-Jen Huang
Mai-Szu Wu
Yung-Ho Hsu
Chia-Te Liao
Cheng-Hsien Chen
author_sort Yu-Wei Chen
collection DOAJ
description Peritoneal dialysis (PD) serves as a home-based kidney replacement therapy with increasing utilization across the globe. However, long-term use of high-glucose-based PD solution incites repeated peritoneal injury and inevitable peritoneal fibrosis, thus compromising treatment efficacy and resulting in ultrafiltration failure eventually. In the present study, we utilized human mesothelial MeT-5A cells for the in vitro experiments and a PD mouse model for in vivo validation to study the pathophysiological mechanisms underneath PD-associated peritoneal fibrosis. High-glucose PD solution (Dianeal 4.25%, Baxter) increased protein expression of mesothelial–mesenchymal transition (MMT) markers, such as N-cadherin and α-SMA in MeT-5A cells, whereas it decreased catalase expression and stimulated the production of reactive oxygen species (ROS). Furthermore, macrophage influx and increased serum pro-inflammatory cytokines, such as IL-1β, MCP-1, and TNF-α, were observed in the PD mouse model. Interestingly, we discovered that oligo-fucoidan, an oligosaccharide extract from brown seaweed, successfully prevented PD-associated peritoneal thickening and fibrosis through antioxidant effect, downregulation of MMT markers, and attenuation of peritoneal and systemic inflammation. Hence, oligo-fucoidan has the potential to be developed into a novel preventive strategy for PD-associated peritoneal fibrosis.
format Article
id doaj-art-e7d62dad39934ef28a6e030ceb728668
institution DOAJ
issn 1660-3397
language English
publishDate 2024-11-01
publisher MDPI AG
record_format Article
series Marine Drugs
spelling doaj-art-e7d62dad39934ef28a6e030ceb7286682025-08-20T02:57:02ZengMDPI AGMarine Drugs1660-33972024-11-01221252910.3390/md22120529Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated FibrosisYu-Wei Chen0Mei-Yi Wu1Nai-Jen Huang2Mai-Szu Wu3Yung-Ho Hsu4Chia-Te Liao5Cheng-Hsien Chen6Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 110, TaiwanDivision of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 235041, TaiwanDepartment of Internal Medicine, Division of Nephrology, Wan Fang Hospital, Taipei Medical University, Taipei 116, TaiwanGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 110, TaiwanGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 110, TaiwanDivision of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 235041, TaiwanGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 110, TaiwanPeritoneal dialysis (PD) serves as a home-based kidney replacement therapy with increasing utilization across the globe. However, long-term use of high-glucose-based PD solution incites repeated peritoneal injury and inevitable peritoneal fibrosis, thus compromising treatment efficacy and resulting in ultrafiltration failure eventually. In the present study, we utilized human mesothelial MeT-5A cells for the in vitro experiments and a PD mouse model for in vivo validation to study the pathophysiological mechanisms underneath PD-associated peritoneal fibrosis. High-glucose PD solution (Dianeal 4.25%, Baxter) increased protein expression of mesothelial–mesenchymal transition (MMT) markers, such as N-cadherin and α-SMA in MeT-5A cells, whereas it decreased catalase expression and stimulated the production of reactive oxygen species (ROS). Furthermore, macrophage influx and increased serum pro-inflammatory cytokines, such as IL-1β, MCP-1, and TNF-α, were observed in the PD mouse model. Interestingly, we discovered that oligo-fucoidan, an oligosaccharide extract from brown seaweed, successfully prevented PD-associated peritoneal thickening and fibrosis through antioxidant effect, downregulation of MMT markers, and attenuation of peritoneal and systemic inflammation. Hence, oligo-fucoidan has the potential to be developed into a novel preventive strategy for PD-associated peritoneal fibrosis.https://www.mdpi.com/1660-3397/22/12/529fibrosismesothelial–mesenchymal transitionMMToligo-fucoidanperitoneal dialysis
spellingShingle Yu-Wei Chen
Mei-Yi Wu
Nai-Jen Huang
Mai-Szu Wu
Yung-Ho Hsu
Chia-Te Liao
Cheng-Hsien Chen
Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis
Marine Drugs
fibrosis
mesothelial–mesenchymal transition
MMT
oligo-fucoidan
peritoneal dialysis
title Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis
title_full Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis
title_fullStr Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis
title_full_unstemmed Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis
title_short Therapeutic Potential of Oligo-Fucoidan in Mitigating Peritoneal Dialysis-Associated Fibrosis
title_sort therapeutic potential of oligo fucoidan in mitigating peritoneal dialysis associated fibrosis
topic fibrosis
mesothelial–mesenchymal transition
MMT
oligo-fucoidan
peritoneal dialysis
url https://www.mdpi.com/1660-3397/22/12/529
work_keys_str_mv AT yuweichen therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis
AT meiyiwu therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis
AT naijenhuang therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis
AT maiszuwu therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis
AT yunghohsu therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis
AT chiateliao therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis
AT chenghsienchen therapeuticpotentialofoligofucoidaninmitigatingperitonealdialysisassociatedfibrosis