PEROXISOME PROLIFERATION AND OXIDATIVE STRESS MEDIATED BY ACTIVATED OXYGEN SPECIES IN PLANT PEROXISOMES

被引:85
作者
PALMA, JM [1 ]
GARRIDO, M [1 ]
RODRIGUEZGARCIA, MI [1 ]
DELRIO, LA [1 ]
机构
[1] CSIC, ESTAC EXPTL ZAIDIN, UNIDAD BIOQUIM VEGETAL, APDO 419, E-18080 GRANADA, SPAIN
关键词
D O I
10.1016/0003-9861(91)90389-Z
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
The existence of a relationship between clofibrate-induced peroxisome proliferation and oxidative stress mediated by activated oxygen species was studied in intact peroxisomes purified from Pisum sativum L. plants. Incubation of leaves with 1 mm clofibrate produced a remarkable increase in the peroxisomal activity of acyl-CoA oxidase and, to a lesser extent, of xanthine oxidase, whereas there was a nearly complete loss of catalase activity and a decrease in Mn-superoxide dismutase. Ultrastructural studies of intact leaves showed that clofibrate induced a five- and twofold proliferation of the peroxisomal and mitochondrial populations, respectively, in comparison with those in control leaves. Prolonged incubation with clofibrate produced considerable alterations in the ultrastructure of cells. In peroxisomal membranes, the NADH-induced generation of O2 - radicals, as well as the lipid peroxidation of membranes, increased as a result of treatment of plants with clofibrate. In intact peroxisomes treated with this hypolipidemic drug, the H2O2 concentration was higher than in peroxisomes from control plants. These results demonstrate that clofibrate stimulates the production of activated oxygen species (O2 - and H2O2) inside peroxisomes, as well as the lipid peroxidation of peroxisomal membranes. This effect is concomitant with a decrease of catalase and Mn-SOD activities, the main peroxisomal enzymatic defenses against H2O2 and O2 -, and indicates that in the toxicity of clofibrate, at the level of peroxisomes, an oxidative stress mechanism mediated by activated oxygen species is involved. © 1991.
引用
收藏
页码:68 / 74
页数:7
相关论文
共 46 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]  
ANGERMULLER S, 1987, EUR J CELL BIOL, V45, P137
[3]  
BEIER K, 1988, EUR J CELL BIOL, V46, P383
[4]  
BOVERIS A, 1984, METHOD ENZYMOL, V105, P429
[5]   CELLULAR PRODUCTION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CHANCE, B ;
OSHINO, N .
BIOCHEMICAL JOURNAL, 1972, 128 (03) :617-&
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]  
Buege J A, 1978, Methods Enzymol, V52, P302
[8]  
CIBELLI A, 1988, CELL MOL BIOL, V34, P191
[9]   DECREASE OF SUPEROXIDE-DISMUTASE AND GLUTATHIONE-PEROXIDASE IN LIVER OF RATS TREATED WITH HYPOLIPIDEMIC DRUGS [J].
CIRIOLO, MR ;
MAVELLI, I ;
ROTILIO, G ;
BORZATTA, V ;
CRISTOFARI, M ;
STANZANI, L .
FEBS LETTERS, 1982, 144 (02) :264-268
[10]   CYTOCHEMICAL STUDY OF CATALASE AND PEROXIDASE IN THE MESOPHYLL OF LOLIUM-RIGIDUM PLANTS TREATED WITH ISOPROTURON [J].
DEFELIPE, MR ;
LUCAS, MM ;
POZUELO, JM .
JOURNAL OF PLANT PHYSIOLOGY, 1988, 132 (01) :67-73