LIVER PEROXISOMES IN NEWBORNS FROM CLOFIBRATE-TREATED RATS .2. A BIOCHEMICAL-STUDY OF THE RECOVERY PERIOD

被引:18
作者
SARTORI, C
STEFANINI, S
CIMINI, A
DIGIULIO, A
CERU, MP
机构
[1] UNIV ROME LA SAPIENZA, DEPT CELLULAR & DEV BIOL, PIAZZALE A MORO 5, I-00185 ROME, ITALY
[2] UNIV LAQUILA, DEPT SCI & BIOMED TECHNOL & BIOMETRY, I-67100 LAQUILA, ITALY
关键词
LIVER PEROXISOMES; CLOFIBRATE; NEWBORN RAT; CATALASE; ACYL-COA BETA-OXIDATION; RECOVERY;
D O I
10.1016/0248-4900(92)90043-Z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fatty-acyl-CoA beta-oxidation (FAO) and catalase activities, as well as membrane fluidity of liver peroxisomes of newborns from normal and clofibrate-treated rats were studied during the recovery period, ie, throughout the first week of postnatal life. In the test animals the enzyme activities, which are significantly higher than controls at birth return to normal levels showing a somewhat different time course with FAO rapidly decreasing to control values within three days but with catalase still higher than controls at day 6. The half-life and degradation rate (K(d)) of FAO are identical to those calculated by us for the whole organelles and to those reported by others for total catalase in normal or clofibrate-treated adult animals in the presence of catalase inhibitors. Soluble catalase shows turnover values which are similar though not identical to those of FAO, while total catalase has a very long half-life and a low K(d). Peroxisomal membrane fluidity, as determined by fluorescence anisotropy of 1-anilinonaphthalene-8-sulfonate (ANS) bound to purified peroxisomal fractions is higher in tests than in controls, recovering normal values within 6 days. Our results demonstrate that liver peroxisomes of rats prenatally exposed to clofibrate return to control conditions within about 1 week. The turnover parameters of enzymes and the membrane fluidity values are discussed in terms of disposal mechanism(s) for the excess of induced peroxisomes.
引用
收藏
页码:315 / 324
页数:10
相关论文
共 53 条
[1]   PARTIAL DISASSEMBLY OF PEROXISOMES [J].
ALEXSON, SEH ;
FUJIKI, Y ;
SHIO, H ;
LAZAROW, PB .
JOURNAL OF CELL BIOLOGY, 1985, 101 (01) :294-304
[2]   ISOLATION OF PEROXISOMES FROM RAT-LIVER USING SUCROSE AND PERCOLL GRADIENTS [J].
APPELKVIST, EL ;
BRUNK, U ;
DALLNER, G .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1981, 5 (04) :203-217
[3]  
BENDAYAN M, 1982, LAB INVEST, V47, P364
[4]   ENZYMATIC CHANGES IN RAT-LIVER ASSOCIATED WITH LOW AND HIGH-DOSES OF A PEROXISOME PROLIFERATOR [J].
BERGE, RK ;
HOSOY, LH ;
AARSLAND, A ;
BAKKE, OM ;
FARSTAD, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1984, 73 (01) :35-41
[5]   PEROXISOME BIOGENESIS REVISITED [J].
BORST, P .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1008 (01) :1-13
[6]  
CERU MP, 1989, 19TH M FEBS ROM
[7]  
CERU MP, 1989, INT J IMMUNOPATH PH, V2, P9
[8]  
CIBELLI A, 1988, CELL MOL BIOL, V34, P191
[9]   POSSIBLE MECHANISMS IN HEPATOCARCINOGENESIS BY THE PEROXISOME PROLIFERATOR DI(2-ETHYLHEXYL)PHTHALATE [J].
CONWAY, JG ;
CATTLEY, RC ;
POPP, JA ;
BUTTERWORTH, BE .
DRUG METABOLISM REVIEWS, 1989, 21 (01) :65-102
[10]   ALTERATIONS IN THE INTEGRITY OF PEROXISOMAL MEMBRANES IN LIVERS OF MICE TREATED WITH PEROXISOME PROLIFERATORS [J].
CRANE, DI ;
ZAMATTIA, J ;
MASTERS, CJ .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1990, 96 (02) :153-161