Toxic response indicators of microcystin-LR in F344 rats following a single-dose treatment

被引:29
作者
Billam, Madhavi [1 ]
Mukhi, Sandeep [1 ]
Tang, Lili [1 ]
Gao, Weimin [1 ]
Wang, Jia-Sheng [1 ]
机构
[1] Texas Tech Univ, Dept Environm Toxicol, Inst Environm & Human Hlth, Lubbock, TX 79409 USA
关键词
microcystin-LR; acute toxicity; F344; rats; PP2A; toxic response indicators;
D O I
10.1016/j.toxicon.2008.01.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Microcystin-LR (MCLR) is the most common hepatotoxic cyanotoxin produced primarily by Microcystis aeruginosa. In this study, young F344 rats were intraperitoneally injected with a single dose (25, 50, 100, and 150 mu g/kg) of MCLR to explore possible toxic effect and toxic response indicators. Acute toxic symptoms, including body weight loss and death, were monitored for 7 days. Mortality reached 100% (9/9) in rats treated with a single MCLR dose of 150 mu g/kg. Histopathological examination showed spot necrosis in the liver of animals treated at low doses, while massive hemorrhage and widespread necrotic foci occurred at higher doses, indicating extensive liver damage. Protein phosphatase 2A (PP2A) expression showed a dose-dependent decrease in the liver. Immunohistochemical localization indicated that nuclear PP2A was affected first, followed by cytoplasmic PP2A. In addition, there was a significant increase in sphingolipid levels at higher doses, indicating the involvement of a ceramide-mediated apoptotic pathway. Expression of apoptosis and cell cycle regulatory proteins like Bax, Bcl2, and Bad showed a dose-dependent decrease. This study demonstrated that treatment with a single dose of MCLR caused liver damage, increased sphingolipid levels, and decreased PP2A expression, which ultimately down-regulated the expression of Bcl2 family proteins. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1068 / 1080
页数:13
相关论文
共 60 条
[1]   PHOSPHORYLATION DETERMINES THE BINDING OF MICROTUBULE-ASSOCIATED PROTEIN-2 (MAP2) TO MICROTUBULES IN LIVING CELLS [J].
BRUGG, B ;
MATUS, A .
JOURNAL OF CELL BIOLOGY, 1991, 114 (04) :735-743
[2]   DIFFERENTIAL PHOSPHORYLATION OF CK8 AND CK18 BY 12-O-TETRADECANOYL-PHORBOL-13-ACETATE IN PRIMARY CULTURES OF MOUSE HEPATOCYTES [J].
CADRIN, M ;
MCFARLANEANDERSON, N ;
AASHEIM, LH ;
KAWAHARA, H ;
FRANKS, DJ ;
MARCEAU, N ;
FRENCH, SW .
CELLULAR SIGNALLING, 1992, 4 (06) :715-722
[3]   Validation of fumonisin biornarkers in F344 rats [J].
Cai, Qingsong ;
Tang, Lili ;
Wang, Jia-Sheng .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 225 (01) :28-39
[4]  
Carmichael W., 1981, WATER ENV ALGAL TOXI
[5]   CYANOBACTERIA SECONDARY METABOLITES - THE CYANOTOXINS [J].
CARMICHAEL, WW .
JOURNAL OF APPLIED BACTERIOLOGY, 1992, 72 (06) :445-459
[6]   Induction of apoptosis in mouse liver by microcystin-LR - A combined transcriptomic, proteomic, and simulation strategy [J].
Chen, T ;
Wang, QS ;
Cui, J ;
Yang, W ;
Shi, Q ;
Hua, ZC ;
Ji, JG ;
Shen, PP .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (07) :958-974
[7]   INTERMEDIATE FILAMENT REORGANIZATION DURING MITOSIS IS MEDIATED BY P34CDC2 PHOSPHORYLATION OF VIMENTIN [J].
CHOU, YH ;
BISCHOFF, JR ;
BEACH, D ;
GOLDMAN, RD .
CELL, 1990, 62 (06) :1063-1071
[8]   Sphingolipids and the immune system [J].
Cinque, B ;
Di Marzio, L ;
Centi, C ;
Di Rocco, C ;
Riccardi, C ;
Cifone, MG .
PHARMACOLOGICAL RESEARCH, 2003, 47 (05) :421-437
[9]   Hepatic gene expression changes in mice associated with prolonged sublethal microcystin exposure [J].
Clark, Shawn P. ;
Davis, Myrtle A. ;
Ryan, Timothy P. ;
Searfoss, George H. ;
Hooser, Stephen B. .
TOXICOLOGIC PATHOLOGY, 2007, 35 (04) :594-605
[10]   Calpain activation after mitochondrial permeability transition in microcystin-induced cell death in rat hepatocytes [J].
Ding, WX ;
Shen, HM ;
Ong, CN .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 291 (02) :321-331