The relationship between the anti-inflammatory effects of curcumin and cellular glutathione content in myelomonocytic cells

被引:65
作者
Strasser, EM [1 ]
Wessner, B [1 ]
Manhart, N [1 ]
Roth, E [1 ]
机构
[1] Med Univ Vienna, Res Labs, Dept Surg, A-1090 Vienna, Austria
关键词
curcumin; antioxidative; prooxidative; anti-inflammatory; glutathione; reactive oxygen species;
D O I
10.1016/j.bcp.2005.05.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oxidative stress plays an important role during inflammatory diseases and recent therapies have focused on antioxidant administration to diminish oxidative stress and to arrest inflammatory processes. In this study, we investigated the impact of the GSH modulating effects of curcumin, a naturally derived polyphenol, on inflammatory processes in myelomonocytic U937 cells. One hour after administration of 10 mu mol/1 curcumin reactive oxygen species (ROS) production was significantly increased in undifferentiated U937 cells (+43%). Twenty-four hour after addition of curcumin, a significantly decreased ROS concentration was found (-32%), whereas GSH (+110%) and GSSG (+88%) content increased. A higher concentration of curcumin (25 mu mol/1) caused an even stronger increase of GSH (+145%) and GSSG (+101%), but significantly decreased percentage of living cells to 84%. The increased GSH content of differentiated U937 cells after pre-incubation with curcumin was associated with lowered ROS production, nuclear factor kappa B (NF kappa B) activation (-34%) and tumor necrosis factor alpha (TNF-alpha) secretion (-51%) after LPS exposure. Curcumin inhibited TNF-alpha formation was also seen after GSH depletion by buthionine sulfoximine (BSO). This study shows that the antioxidative effects of curcumin are preceded by an oxidative stimulus, which is time and dose-dependent. Excessive concentrations of curcumin may even harm cells, as cell viability was decreased, in spite of elevated GSH contents. There was no clear relationship between intracellular GSH concentrations and the anti-inflammatory effects of curcumin. (c):) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:552 / 559
页数:8
相关论文
共 36 条
  • [1] CHEMOPREVENTIVE EFFECT OF TURMERIC AGAINST STOMACH AND SKIN TUMORS INDUCED BY CHEMICAL CARCINOGENS IN SWISS MICE[J]. AZUINE, MA;BHIDE, SV. NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1992(01)
  • [2] Curcumin-induced inhibition of cellular reactive oxygen species generation: Novel therapeutic implications[J]. Balasubramanyam, M;Koteswari, AA;Kumar, RS;Monickaraj, SF;Maheswari, JU;Mohan, V. JOURNAL OF BIOSCIENCES, 2003(06)
  • [3] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [4] INHIBITION OF TUMOR-NECROSIS-FACTOR BY CURCUMIN, A PHYTOCHEMICAL[J]. CHAN, MMY. BIOCHEMICAL PHARMACOLOGY, 1995(11)
  • [5] Curcumin inhibits UV irradiation-induced oxidative stress and apoptotic biochemical changes in human epidermoid carcinoma A431 cells[J]. Chan, WH;Wu, CC;Yu, JS. JOURNAL OF CELLULAR BIOCHEMISTRY, 2003(02)
  • [6] Cheng AL, 2001, ANTICANCER RES, V21, P2895
  • [7] Curcumin alters EpRE and AP-1 binding complexes and elevates glutamate-cysteine ligase gene expression[J]. Dickinson, DA;Iles, KE;Zhang, HQ;Blank, V;Forman, HJ. FASEB JOURNAL, 2003(01)
  • [8] Induction of apoptosis by curcumin:: mediation by glutathione S-transferase P1-1 inhibition[J]. Duvoix, A;Morceau, F;Delhalle, S;Schmitz, M;Schnekenburger, M;Galteau, MM;Dicato, M;Diederich, M. BIOCHEMICAL PHARMACOLOGY, 2003(08)
  • [9] Exner R, 2000, WIEN KLIN WOCHENSCHR, V112, P610
  • [10] FLESCHER E, 1994, J IMMUNOL, V153, P4880