Differential regulation of phosphatidylinositol 3-kinase/Akt, mitogen-activated protein kinase, and AMP-activated protein kinase pathways during menadione-induced oxidative stress in the kidney of young and old rats

被引:37
作者
Jin, QR
Jhun, BS
Lee, SH
Lee, J
Pi, YH
Cho, YH
Baik, HH
Kang, I [1 ]
机构
[1] Kyung Hee Univ, Sch Med, Med Res Ctr, Seoul 130701, South Korea
[2] Yan Bian Univ, Coll Med, Dept Anat, Yanji 133000, Jilin, Peoples R China
[3] Dongseo Univ, Dept Biotechnol, Pusan 616010, South Korea
[4] Kyung Hee Univ, Sch Med, Dept Biochem & Mol Biol, Seoul 130701, South Korea
关键词
aging; reactive oxygen species; apoptosis; rat kidney; menadione; PI; 3-kinase; MAPK; PTEN; AMPK; p53;
D O I
10.1016/j.bbrc.2004.01.093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated regulation of various signal transduction pathways during oxidative stresses in the kidney of young and aged rats. Menadione-induced regulation of molecules in PI 3-kinase, MAPK, and AMPK pathways was determined in the young (2 months) and old (24 months) groups. PI 3-kinase activity and Akt phosphorylation were significantly reduced in the old compared with the young. PTEN tumor suppressor was also lower in its expression and phosphorylation levels in the old. Response of the molecules in PI 3-kinase pathway to menadione was minimized. In contrast, over 5-fold induction of ERK1/2 phosphorylation by menadione was observed in both groups. On the other hand, basal activities as well as menadione-induced activities of JNK1 and AMPK were higher in the old than in the young. While p27(Kip1), p53, and p21(Waf1) were slightly increased by menadione in both groups, the basal induction level in the old was considerably higher. In conclusion, the results suggest that the age-related down-regulation of PI 3-kinase/Akt pathway and up-regulation of JNK1, AMPK, and p53 pathways may be responsible for the increased susceptibility to oxidative stress. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:555 / 561
页数:7
相关论文
共 33 条
[1]   Tumor suppressors and oncogenes in cellular senescence [J].
Bringold, F ;
Serrano, M .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (03) :317-329
[2]   Bypass of senescence after disruption of p21(CIP1/WAF1) gene in normal diploid human fibroblasts [J].
Brown, JP ;
Wei, WY ;
Sedivy, JM .
SCIENCE, 1997, 277 (5327) :831-834
[3]   Jun NH2-terminal kinase phosphorylation of p53 on Thr-81 is important for p53 stabilization and transcriptional activities in response to stress [J].
Buschmann, T ;
Potapova, O ;
Bar-Shira, A ;
Ivanov, VN ;
Fuchs, SY ;
Henderson, S ;
Fried, VA ;
Minamoto, T ;
Alarcon-Vargas, D ;
Pincus, MR ;
Gaarde, WA ;
Holbrook, NJ ;
Shiloh, Y ;
Ronai, Z .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (08) :2743-2754
[4]   Cardiac and renal toxicity of menadione in rat [J].
Chiou, TJ ;
Zhang, J ;
Ferrans, VJ ;
Tzeng, WF .
TOXICOLOGY, 1997, 124 (03) :193-202
[5]   Inhibition of the phosphoinositide 3-kinase pathway induces a senescence-like arrest mediated by p27Kip1 [J].
Collado, M ;
Medema, RH ;
García-Cao, I ;
Dubuisson, MLN ;
Barradas, M ;
Glassford, J ;
Rivas, C ;
Burgering, BMT ;
Serrano, M ;
Lam, EWF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (29) :21960-21968
[6]   Effect of age on vanadium nephrotoxicity in rats [J].
de la Torre, A ;
Granero, S ;
Mayayo, E ;
Corbella, J ;
Domingo, JL .
TOXICOLOGY LETTERS, 1999, 105 (01) :75-82
[7]   The tumor-suppressor activity of PTEN is regulated by its carboxyl-terminal region [J].
Georgescu, MM ;
Kirsch, KH ;
Akagi, T ;
Shishido, T ;
Hanafusa, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (18) :10182-10187
[8]   Does oxidative damage to DNA increase with age? [J].
Hamilton, ML ;
Van Remmen, H ;
Drake, JA ;
Yang, H ;
Guo, ZM ;
Kewitt, K ;
Walter, CA ;
Richardson, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10469-10474
[9]   Hyperglycemia-induced apoptosis in human umbilical vein endothelial cells - Inhibition by the AMP-activated protein kinase activation [J].
Ido, Y ;
Carling, D ;
Ruderman, N .
DIABETES, 2002, 51 (01) :159-167
[10]  
Ikeyama S, 2001, FASEB J, V15, P114, DOI 10.1096/fj.01-0409fje