Literature DB >> 9041217

In vitro simulation of the effect of peritoneal dialysis solution on mesothelial cells.

A Breborowicz1, H Rodela, J Karoń, L Martis, D G Oreopoulos.   

Abstract

All previous in vitro biocompatibility tests of peritoneal dialysis fluids have shown that these have inhibitory effects on the function of peritoneal mesothelium. This report presents results from in vitro experiments performed to study the effect of dialysis fluids (Dianeal 1.36 and Dianeal 3.86; Baxter, Round Lake, IL) on the function of mesothelial cells under conditions that simulate the in vivo state of these solutions in the peritoneal cavity. Thus, cells were initially exposed only to the unused fluids that were thereafter gradually diluted (over 4 hours) with pooled effluent dialysate from continuous ambulatory peritoneal dialysis patients. During the following 20 hours, cells were incubated in a mixture of unused fluid (10% vol/vol) and dialysate effluent (90% vol/vol). The mesothelial cells exposed to dialysis fluids under such conditions became activated cells compared with exposed to dialysate effluent (control) alone. Thus, synthesis by mesothelial cells of all tested substances was enhanced during exposure of the mesothelium to the dialysis fluids: interleukin-6: Dianeal 1.36, +257%; Dianeal 3.86, +181% (both P < 0.05); hyaluronic acid: Dianeal 1.36, +72%; Dianeal 3.86, +63% (both P < 0.05); tissue plasminogen activator: Dianeal 3.86, +33% (P < 0.05); and plasminogen activator/inhibitor-1: Dianeal 1.36, +28%; Dianeal 3.86, +38% (both P < 0.05). Our results show that the peritoneal mesothelium becomes activated when it is exposed to acidic, hyperosmotic dialysis fluids diluted with the dialysate effluent, in a manner that imitates the in vivo changes in these solutions during their intraperitoneal dwell.

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Year:  1997        PMID: 9041217     DOI: 10.1016/s0272-6386(97)90202-x

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  4 in total

1.  Enhancement of port site metastasis by hyaluronic acid under CO2 pneumoperitoneum in a murine model.

Authors:  K Yamaguchi; Y Hirabayashi; A Shiromizu; N Shiraishi; Y Adachi; S Kitano
Journal:  Surg Endosc       Date:  2001-02-06       Impact factor: 4.584

2.  Impact of 3,4-dideoxyglucosone-3-ene (3,4-DGE) on cytotoxicity of acidic heat-sterilized peritoneal dialysis fluid.

Authors:  Tadashi Tomo; Eiji Okabe; Takashi Yamamoto; Shinji Namoto; Tomohiko Iwashita; Kazuhiro Matsuyama; Jun-ichi Kadota
Journal:  J Artif Organs       Date:  2007-03-23       Impact factor: 1.731

3.  Hyaluronic acid secretion during carbon dioxide pneumoperitoneum and its association with port-site metastasis in a murine model.

Authors:  K Yamaguchi; Y Hirabayashi; T Suematsu; N Shiraishi; Y Adachi; S Kitano
Journal:  Surg Endosc       Date:  2001-01       Impact factor: 4.584

4.  Protection of trocar sites from gallbladder cancer implantation by sodium hyaluronate carboxymethylcellulose-based bioresorbable membrane (Seprafilm) in a murine model [corrected].

Authors:  T Sasaki; H Shimura; T Tanaka; K Nakashima; K Matsuo; S Ikeda
Journal:  Surg Endosc       Date:  2003-12-29       Impact factor: 4.584

  4 in total

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