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      Targeting cannabinoid signaling for peritoneal dialysis-induced oxidative stress and fibrosis

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          Abstract

          Long-term exposure to bioincompatible peritoneal dialysis (PD) solutions frequently results in peritoneal fibrosis and ultrafiltration failure, which limits the life-long use of and leads to the cessation of PD therapy. Therefore, it is important to elucidate the pathogenesis of peritoneal fibrosis in order to design therapeutic strategies to prevent its occurrence. Peritoneal fibrosis is associated with a chronic inflammatory status as well as an elevated oxidative stress (OS) status. Beyond uremia per se, OS also results from chronic exposure to high glucose load, glucose degradation products, advanced glycation end products, and hypertonic stress. Therapy targeting the cannabinoid (CB) signaling pathway has been reported in several chronic inflammatory diseases with elevated OS. We recently reported that the intra-peritoneal administration of CB receptor ligands, including CB 1 receptor antagonists and CB 2 receptor agonists, ameliorated dialysis-related peritoneal fibrosis. As targeting the CB signaling pathway has been reported to be beneficial in attenuating the processes of several chronic inflammatory diseases, we reviewed the interaction among the cannabinoid system, inflammation, and OS, through which clinicians ultimately aim to prolong the peritoneal survival of PD patients.

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          Most cited references102

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          The elephant in uremia: oxidant stress as a unifying concept of cardiovascular disease in uremia.

          Cardiovascular disease is the leading cause of mortality in uremic patients. In large cross-sectional studies of dialysis patients, traditional cardiovascular risk factors such as hypertension and hypercholesterolemia have been found to have low predictive power, while markers of inflammation and malnutrition are highly correlated with cardiovascular mortality. However, the pathophysiology of the disease process that links uremia, inflammation, and malnutrition with increased cardiovascular complications is not well understood. We hereby propose the hypothesis that increased oxidative stress and its sequalae is a major contributor to increased atherosclerosis and cardiovascular morbidity and mortality found in uremia. This hypothesis is based on studies that conclusively demonstrate an increased oxidative burden in uremic patients, before and particularly after renal replacement therapies, as evidenced by higher concentrations of multiple biomarkers of oxidative stress. This hypothesis also provides a framework to explain the link that activated phagocytes provide between oxidative stress and inflammation (from infectious and non-infections causes) and the synergistic role that malnutrition (as reflected by low concentrations of albumin and/or antioxidants) contributes to the increased burden of cardiovascular disease in uremia. We further propose that retained uremic solutes such as beta-2 microglobulin, advanced glycosylated end products (AGE), cysteine, and homocysteine, which are substrates for oxidative injury, further contribute to the pro-atherogenic milieu of uremia. Dialytic therapy, which acts to reduce the concentration of oxidized substrates, improves the redox balance. However, processes related to dialytic therapy, such as the prolonged use of catheters for vascular access and the use of bioincompatible dialysis membranes, can contribute to a pro-inflammatory and pro-oxidative state and thus to a pro-atherogenic state. Anti-oxidative therapeutic strategies for patients with uremia are in their very early stages; nonetheless, early studies demonstrate the potential for significant efficacy in reducing cardiovascular complications.
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            Peritoneal dialysis and epithelial-to-mesenchymal transition of mesothelial cells.

            During continuous ambulatory peritoneal dialysis, the peritoneum is exposed to bioincompatible dialysis fluids that cause denudation of mesothelial cells and, ultimately, tissue fibrosis and failure of ultrafiltration. However, the mechanism of this process has yet to be elucidated. Mesothelial cells isolated from effluents in dialysis fluid from patients undergoing continuous ambulatory peritoneal dialysis were phenotypically characterized by flow cytometry, confocal immunofluorescence, Western blotting, and reverse-transcriptase polymerase chain reaction. These cells were compared with mesothelial cells from omentum and treated with various stimuli in vitro to mimic the transdifferentiation observed during continuous ambulatory peritoneal dialysis. Results were confirmed in vivo by immunohistochemical analysis performed on peritoneal-biopsy specimens. Soon after dialysis is initiated, peritoneal mesothelial cells undergo a transition from an epithelial phenotype to a mesenchymal phenotype with a progressive loss of epithelial morphology and a decrease in the expression of cytokeratins and E-cadherin through an induction of the transcriptional repressor snail. Mesothelial cells also acquire a migratory phenotype with the up-regulation of expression of alpha2 integrin. In vitro analyses point to wound repair and profibrotic and inflammatory cytokines as factors that initiate mesothelial transdifferentiation. Immunohistochemical studies of peritoneal-biopsy specimens from patients undergoing continuous ambulatory peritoneal dialysis demonstrate the expression of the mesothelial markers intercellular adhesion molecule 1 and cytokeratins in fibroblast-like cells entrapped in the stroma, suggesting that these cells stemmed from local conversion of mesothelial cells. Our results suggest that mesothelial cells have an active role in the structural and functional alteration of the peritoneum during peritoneal dialysis. The findings suggest potential targets for the design of new dialysis solutions and markers for the monitoring of patients. Copyright 2003 Massachusetts Medical Society
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              Cannabinoid pharmacology: the first 66 years.

              Research into the pharmacology of individual cannabinoids that began in the 1940s, several decades after the presence of a cannabinoid was first detected in cannabis, is concisely reviewed. Also described is how this pharmacological research led to the discovery of cannabinoid CB(1) and CB(2) receptors and of endogenous ligands for these receptors, to the development of CB(1)- and CB(2)-selective agonists and antagonists and to the realization that the endogenous cannabinoid system has significant roles in both health and disease, and that drugs which mimic, augment or block the actions of endogenously released cannabinoids must have important therapeutic applications. Some goals for future research are identified.
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                Author and article information

                Journal
                World J Nephrol
                WJN
                World Journal of Nephrology
                Baishideng Publishing Group Inc
                2220-6124
                6 May 2017
                6 May 2017
                : 6
                : 3
                : 111-118
                Affiliations
                Chih-Yu Yang, Der-Cherng Tarng, Division of Nephrology, Department of Medicine, Taipei Veterans General Hospital, Taipei 11217, Taiwan
                Chih-Yu Yang, Oscar Kuang-Sheng Lee, Der-Cherng Tarng, An-Hang Yang, School of Medicine, National Yang-Ming University, Taipei 11221, Taiwan
                Chih-Yu Yang, Oscar Kuang-Sheng Lee, Der-Cherng Tarng, An-Hang Yang, Institute of Clinical Medicine, National Yang-Ming University, Taipei 11221, Taiwan
                Yat-Pang Chau, Faculty of Medicine, Mackay Medical College, New Taipei City 25245, Taiwan
                Ann Chen, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan
                Oscar Kuang-Sheng Lee, Department of Orthopedic Surgery, Taipei City Hospital, Taipei 10629, Taiwan
                Oscar Kuang-Sheng Lee, Stem Cell Research Center, National Yang-Ming University, Taipei 11221, Taiwan
                Oscar Kuang-Sheng Lee, Department of Medical Research and Department of Orthopedic Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan
                An-Hang Yang, Department of Pathology, Taipei Veterans General Hospital, Taipei 11217, Taiwan
                Author notes

                Author contributions: All authors contributed to this paper.

                Supported by The Ministry Of Science and Technology, Taiwan, Nos. NSC 96-2628-B-075-003-MY3, MOST 104-2314-B-075-031, and MOST 105-2628-B-075-008-MY3 ; a grant from Taipei Veterans General Hospital, Taipei, Taiwan, No. V106D25-003-MY3-1; Taipei Veterans General Hospital, National Yang-Ming University Excellent Physician Scientists Cultivation Program, No. 103-V-B-024.

                Correspondence to: Dr. An-Hang Yang, Institute of Clinical Medicine, National Yang-Ming University, No. 201, Section 2, Shih-Pai Road, Taipei 11221, Taiwan. ahyang@ 123456vghtpe.gov.tw

                Telephone: +886-2-28757090 Fax: +886-2-28757056

                Article
                jWJN.v6.i3.pg111
                10.5527/wjn.v6.i3.111
                5424432
                28540200
                fba8042e-314c-4825-9c46-867742756b6e
                ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.

                This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.

                History
                : 4 November 2016
                : 28 January 2017
                : 18 February 2017
                Categories
                Review

                reactive oxygen species,peritoneal fibrosis,peritoneal dialysis,cannabinoid signaling,oxidative stress

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