The hepatoprotective effect of putrescine against cadmium-induced acute liver injury

被引:35
作者
Tzirogiannis, KN
Panoutsopoulos, GI
Demonakou, MD
Papadimas, GK
Kondyli, VG
Kourentzi, KT
Hereti, RI
Mykoniatis, MG
机构
[1] Univ Athens, Sch Med, Dept Expt Pharmacol, GR-11527 Athens, Greece
[2] Sismangolion GD Hosp, Histopathol Lab, Athens 15127, Greece
关键词
apoptosis; cadmium; hepatotoxicity; necrosis; peliosis; putrescine;
D O I
10.1007/s00204-004-0549-0
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The hepatoprotective effect of putrescine against cadmium liver injury was investigated. Male Wistar rats were injected with a dose of cadmium (6.5 mg CdCl2/kg bodyweight, intraperitoneally). Normal saline (group 1) or putrescine (300 mumol/kg bodyweight; group 11) were injected 2, 5 and 8 h later. A number of animals of both groups were killed 0, 12, 16, 24, 48 or 60 h after cadmium intoxication. Liver tissue was histologically assessed for necrosis, apoptosis, peliosis, mitoses, and inflammatory infiltration. Apoptosis was also quantified by the TUNEL assay for hepatocytes and nonparenchymal liver cells. The discrimination between hepatic cell subpopulations was achieved histochemically. The mitotic index in hematoxylin-cosinstained sections and by the immunochemical detection of Ki67 nuclear antigen, 3 H-thymidine incorporation into hepatic DNA, and hepatic thymidine kinase activity were all used as indices of liver regeneration. Both hepatocyte apoptosis and liver necrosis evolved in a biphasic temporal pattern. Nonparenchymal cell apoptosis and peliosis hepatis evolved in a monophasic pattern and were correlated closely. Putrescine administration totally reversed liver necrosis and hepatocyte apoptosis. The time profile of nonparenchymal apoptosis was altered and peliosis hepatis was also totally attenuated. In conclusion, putrescine protected hepatocytes and modulated the mechanism of cadmium-induced acute hepatotoxicity.
引用
收藏
页码:321 / 329
页数:9
相关论文
共 40 条
[1]   STABILIZATION OF ERYTHROCYTE-MEMBRANES BY POLYAMINES [J].
BALLAS, SK ;
MOHANDAS, N ;
MARTON, LJ ;
SHOHET, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (07) :1942-1946
[2]   SPERMINE PREVENTS ENDONUCLEASE ACTIVATION AND APOPTOSIS IN THYMOCYTES [J].
BRUNE, B ;
HARTZELL, P ;
NICOTERA, P ;
ORRENIUS, S .
EXPERIMENTAL CELL RESEARCH, 1991, 195 (02) :323-329
[3]   Enzyme activity alteration by cadmium administration to rats: The possibility of iron involvement in lipid peroxidation [J].
Casalino, E ;
Sblano, C ;
Landriscina, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 346 (02) :171-179
[4]   Toxic metals stimulate inflammatory cytokines in hepatocytes through oxidative stress mechanisms [J].
Dong, WM ;
Simeonova, PP ;
Gallucci, R ;
Matheson, J ;
Flood, L ;
Wang, SY ;
Hubbs, A ;
Luster, MI .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 151 (02) :359-366
[5]   TIME COURSE OF CADMIUM-INDUCED ULTRASTRUCTURAL-CHANGES IN RAT-LIVER [J].
DUDLEY, RE ;
SVOBODA, DJ ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1984, 76 (01) :150-160
[6]   ACUTE EXPOSURE TO CADMIUM CAUSES SEVERE LIVER-INJURY IN RATS [J].
DUDLEY, RE ;
SVOBODA, DJ ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1982, 65 (02) :302-313
[7]   Oxidative damage to mitochondrial DNA and glutathione oxidation in apoptosis:: studies in vivo and in vitro [J].
Esteve, JM ;
Mompo, J ;
De La Asuncion, JG ;
Sastre, J ;
Asensi, M ;
Boix, J ;
Viña, JR ;
Viña, J ;
Pallardó, FV .
FASEB JOURNAL, 1999, 13 (09) :1055-1064
[8]  
Fowler BA, 1991, CADMIUM HLTH TOXICOL, P159
[9]   Cadmium-induced apoptosis in mouse liver [J].
Habeebu, SSM ;
Liu, J ;
Klaassen, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 149 (02) :203-209
[10]   ROLE OF POLYAMINES IN THE CONTROL OF CELL-PROLIFERATION AND DIFFERENTIATION [J].
HEBY, O .
DIFFERENTIATION, 1981, 19 (01) :1-20