Activation of mitogen activated protein kinase (MAPK) during D-galactosamine intoxication in the rat liver

被引:14
作者
Nishioka, H [1 ]
Kishioka, T [1 ]
Iida, C [1 ]
Fujii, K [1 ]
Ichi, I [1 ]
Kojo, S [1 ]
机构
[1] Nara Womens Univ, Dept Food Sci & Nutr, Nara 6308506, Japan
关键词
ERK; galactosamine; JNK; MAPK; oxidative stress; p38; vitamin C;
D O I
10.1016/j.bmcl.2006.02.057
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A significant increase in plasma glutamate-oxaloacetate transaminase and glutamate-pyruvate transaminase was observed 6 It after intraperitoneal administration Of D-galactosamine (D-Galn). Three hours after administration Of D-Galn, the vitamin C concentration in the liver decreased significantly compared to that in a control group and thereafter the hepatic vitamin C concentration remained at a significantly lower level. Phosphorylated JNK (C-Jun NH2-terminal kinase) and phosphorylated ERK (extracellular signal-regulated kinase) started increasing 3 h after D-Galn treatment and remained at a high level for 6-12 It after the treatment, while phosphorylated p38 MAPK increased significantly 6 It after D-Galn administration. These results indicated that oxidative stress and the activation of JNK. and ERK took place almost simultaneously, followed by the activation of p38 MAPK. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3019 / 3022
页数:4
相关论文
共 28 条
[1]   Oxidant-induced hepatocyte injury from menadione is regulated by ERK and AP-1 signaling [J].
Czaja, MJ ;
Liu, HL ;
Wang, YJ .
HEPATOLOGY, 2003, 37 (06) :1405-1413
[2]   Fibroblast growth factor-2 suppression of tumor necrosis factor alpha-mediated apoptosis requires Ras and the activation of mitogen-activated protein kinase [J].
Gardner, AM ;
Johnson, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :14560-14566
[3]   Liver protection from apoptosis requires both blockage of initiator caspase activities and inhibition of ASK1/JNK pathway via glutathione S-transferase regulation [J].
Gilot, D ;
Loyer, P ;
Corlu, A ;
Glaise, D ;
Lagadic-Gossmann, D ;
Atfi, A ;
Morel, F ;
Ichijo, H ;
Guguen-Guillouzo, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) :49220-49229
[4]   Mixed lineage kinase 3 (MLK3)-activated p38 MAP kinase mediates transforming growth factor-β-induced apoptosis in hepatoma cells [J].
Kim, KY ;
Kim, BC ;
Xu, ZL ;
Kim, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (28) :29478-29484
[5]   Hypoosmotic stress activates p38, ERK 1 and 2, and SAPK/JNK in rat hepatocytes [J].
Kim, RD ;
Darling, CE ;
Cerwenka, H ;
Chari, RS .
JOURNAL OF SURGICAL RESEARCH, 2000, 90 (01) :58-66
[6]   SPECIFIC DETERMINATION OF ASCORBIC-ACID WITH CHEMICAL DERIVATIZATION AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
KISHIDA, E ;
NISHIMOTO, Y ;
KOJO, S .
ANALYTICAL CHEMISTRY, 1992, 64 (13) :1505-1507
[7]   P38 mitogen-activated protein kinase inhibition attenuates ischemia-reperfusion injury of the rat liver [J].
Kobayashi, M ;
Takeyoshi, I ;
Yoshinari, D ;
Matsumoto, K ;
Morishita, Y .
SURGERY, 2002, 131 (03) :344-349
[8]   Vitamin C: Basic metabolism and its function as an index of oxidative stress [J].
Kojo, S .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (08) :1041-1064
[9]   Signaling by the germinal center kinase family of protein kinases [J].
Kyriakis, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5259-5262
[10]   Sounding the alarm: Protein kinase cascades activated by stress and inflammation [J].
Kyriakis, JM ;
Avruch, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (40) :24313-24316