PYRUVATE NEUTRALIZES PERITONEAL DIALYSATE CYTOTOXICITY - MAINTAINED INTEGRITY AND PROLIFERATION OF CULTURED HUMAN MESOTHELIAL CELLS

被引:40
|
作者
BRUNKHORST, R
MAHIOUT, A
机构
[1] Division of Nephrology, Hannover Medical School, Hannover
[2] Division of Nephrology, Medical School Hannover, 30625 Hannover
关键词
D O I
10.1038/ki.1995.282
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Toxic effects of commercially available peritoneal dialysate (PD) fluid include damage to mesothelial cells (MC), causing a severely disturbed proliferation of cultured MC. We investigated the injury to the cell membrane (by release of lactate dehydrogenase, LDH), the proliferation (by cell counts and by H-3-thymidine incorporation), and optional the cytokine generation (by IL-1 receptor-antagonist production, IL-1 ra) of cultured human MC during the 48 hours after a 30 minute exposure to PD containing either 35 mmol/liter sodium lactate or sodium pyruvate. All solutions had a pH of 5.2 to 5.6 and were composed as standard PD. Glucose contents of 1.36 and 3.86 mmol/liter were tested. After exposure to the lactate-PD containing 1.36% glucose, LDH activity was increased by more than 30%, proliferation of MC was inhibited by more than 30%, and IL-1 ra production was reduced significantly when compared to pyruvate-PD and the control solution. After preincubation with 3.86% glucose containing PD, all negative effects became even more pronounced in the lactate group whereas the MC maintained their integrity, rate of proliferation and IL-1 ra release after pre-exposure to pyruvate containing PD. These results suggest that the acute toxic effects of commercially available PD on the integrity, proliferation and IL-1 ra production of MC can be avoided by the use of sodium pyruvate instead of sodium lactate.
引用
收藏
页码:177 / 181
页数:5
相关论文
共 50 条
  • [1] PYRUVATE AS NONTOXIC PERITONEAL DIALYSATE (PD) BUFFER - MAINTAINED MESOTHELIAL CELL (MC) INTEGRITY AND PROLIFERATION
    BRUNKHORST, R
    MAHIOUT, A
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1994, 5 (03): : 410 - 410
  • [2] PYRUVATE ANIONS NEUTRALIZE PERITONEAL DIALYSATE CYTOTOXICITY
    MAHIOUT, A
    BRUNKHORST, R
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 1995, 10 (03) : 391 - 394
  • [3] Synthesis of hyaluronic acid by human peritoneal mesothelial cells: Effect of cytokines and dialysate
    Breborowicz, A
    Korybalska, K
    Grzybowski, A
    WieczorowskaTobis, K
    Martis, L
    Oreopoulos, DG
    PERITONEAL DIALYSIS INTERNATIONAL, 1996, 16 (04): : 374 - 378
  • [4] Modulation of perlecan synthesis in human peritoneal mesothelial cells (HPMC) by peritoneal dialysate and heparin.
    Yung, S
    Chen, C
    Lai, KN
    Chan, TM
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 : 536A - 537A
  • [5] CYTOTOXICITY OF OXIDANTS AND ASBESTOS FIBERS IN CULTURED HUMAN MESOTHELIAL CELLS
    KINNULA, VL
    AALTO, K
    RAIVIO, KO
    WALLES, S
    LINNAINMAA, K
    FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (02) : 169 - 176
  • [6] Prostaglandin synthesis of cultured human peritoneal mesothelial cells.
    Kang, DH
    Choi, KB
    Yoon, KI
    KIDNEY INTERNATIONAL, 1999, 55 (04) : 1604 - 1604
  • [7] Effect of pH and glucose on cultured human peritoneal mesothelial cells
    Shao, JC
    Yorioka, N
    Nishida, Y
    Yamakido, M
    SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 1999, 33 (04): : 248 - 256
  • [8] Effect of haluronan-supplemented dialysate on in vitro function of human peritoneal mesothelial cells
    Breborowicz, A
    Pyda, M
    Moberly, J
    Martis, L
    Oreopoulos, D
    AMERICAN JOURNAL OF NEPHROLOGY, 2004, 24 (03) : 316 - 321
  • [9] Effect of glucose on intercellular junctions of cultured human peritoneal mesothelial cells
    Ito, T
    Yorioka, N
    Yamamoto, M
    Kataoka, K
    Yamakido, M
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2000, 11 (11): : 1969 - 1979
  • [10] CYTOTOXICITY AND ANAPHASE ABERRATIONS INDUCED BY MINERAL FIBERS IN CULTURED HUMAN MESOTHELIAL CELLS
    PELIN, K
    HUSGAFVELPURSIAINEN, K
    VALLAS, M
    VANHALA, E
    LINNAINMAA, K
    TOXICOLOGY IN VITRO, 1992, 6 (05) : 445 - 450