Synergistic cytotoxicity of acidity and 3,4-dideoxyglucosone-3-ene under the existence of lactate in peritoneal dialysis fluid

被引:12
作者
Tomo, T [1 ]
Okabe, E [1 ]
Yamamoto, T [1 ]
Namoto, S [1 ]
Iwashita, T [1 ]
Matsuyama, K [1 ]
Kadota, J [1 ]
Nasu, M [1 ]
机构
[1] Oita Univ, Fac Med, Dept Infect Dis, Dept Internal Med 2, Oita 8795593, Japan
关键词
human peritoneal mesothelial cells; lactate; peritoneal dialysis fluid; 3,4-dideoxyglucosone-3-ene(3,4-DGE); synergistic cytotoxicity;
D O I
10.1111/j.1774-9987.2005.00228.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Of the non-physiological compounds in glucoserich peritoneal dialysis fluid, we investigated the synergistic cytotoxicity of acidity and 3,4-Dideoxyglucosone-3ene(3,4-DGE) under the existence of lactate using human peritoneal mesothelial cells (HPMC). The effect of pH on cell viability at various levels of pH (5.5, 6.7, 7.15), with or without lactate was examined by adding 1N-HCl to phosphate buffer solution. We also examined the cytotoxic effects of 3,4-DGE and pH (5.5, 6.7 or 7.15). Additionally, we compared the cytotoxic effects of 3,4-DGE and pH (5.5, 6.7 or 7.15) under existence of lactate (40meq/L) or absence of lactate. The cells were exposed to these solutions for 2 or 4 h. Cell viability was determined by MTT (3-[4, 5 -dim ethylthiazol-2-yl] -2, 5-diphenylterazolium bromide) assay. 3,4-DGE or acidic solution alone had no significant effects on MTT viability under the absence of lactate. However, acidic solutions containing 3,4-DGE significantly decreased MTT viability under the existence of lactate. The MTT viability of HPMC was not decreased by 3,4-DGE or acidity alone under the absence of lactate. However, the combination of acidity and 3,4-DGE markedly decreased MTT viability under the existence of lactate, strongly suggesting the synergistic cytotoxicity of 3,4-DGE and acidity under the existence of lactate.
引用
收藏
页码:182 / 187
页数:6
相关论文
共 25 条
  • [1] DEGRADATION OF CARBOHYDRATES .3. UNSATURATED HEXOSONES
    ANET, EFL
    [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1962, 15 (03) : 503 - &
  • [2] ENERGY-METABOLISM OF HUMAN-NEUTROPHILS DURING PHAGOCYTOSIS
    BORREGAARD, N
    HERLIN, T
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (03) : 550 - 557
  • [3] In vitro simulation of the effect of peritoneal dialysis solution on mesothelial cells
    Breborowicz, A
    Rodela, H
    Karon, J
    Martis, L
    Oreopoulos, DG
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1997, 29 (03) : 404 - 409
  • [4] CARMICHAEL J, 1987, CANCER RES, V47, P936
  • [5] Two-stage isolation procedure for obtaining homogenous populations of microvascular endothelial and mesothelial cells from human omentum
    ChungWelch, N
    Patton, WF
    Shepro, D
    Cambria, RP
    [J]. MICROVASCULAR RESEARCH, 1997, 54 (02) : 121 - 134
  • [6] De Vriese AS, 2001, PERITON DIALYSIS INT, V21, pS9
  • [7] Di Paolo N, 1993, Perit Dial Int, V13 Suppl 2, pS109
  • [8] FUMINORI K, 1994, J AGR FOOD CHEM, V42, P2068
  • [9] Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis
    Horiuchi, T
    Miyamoto, K
    Miyamoto, S
    Fujita, M
    Sano, N
    Minamiyama, K
    Fujimura, Y
    Nagasawa, K
    Otsuka, C
    Ohta, Y
    [J]. KIDNEY INTERNATIONAL, 2003, 64 (06) : 2280 - 2290
  • [10] Lage C, 2000, PERITON DIALYSIS INT, V20, pS28