CHANGE IN FLUIDITY OF BRAIN ENDOPLASMIC-RETICULUM MEMBRANES BY OXYGEN-FREE RADICALS - A PROTECTIVE EFFECT OF STOBADINE, ALPHA-TOCOPHEROL ACETATE, AND BUTYLATED HYDROXYTOLUENE

被引:39
作者
KAPLAN, P
RACAY, P
LEHOTSKY, J
MEZESOVA, V
机构
[1] Jessenius Medical Faculty, Department of Biochemistry, Comenius University, Martin, SK-036 01
关键词
ENDOPLASMIC RETICULUM; FREE RADICALS; LIPID PEROXIDATION; MEMBRANE FLUIDITY; STOBADINE; BRAIN;
D O I
10.1007/BF00969693
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
Effect of various oxygen free radical generating systems and an oxidant H2O2 on brain endoplasmic reticulum (ER) membrane fluidity was examined using fluorescent membrane probe 1,6-diphenyl-1,3,5-hexatriene, DPH. The relative potency of free radical generating systems to decrease membrane fluidity increased in this order: FeCl3-EDTA, FeSO4-EDTA, FeSO4-EDTA/hydrogen peroxide. Potency to decrease membrane fluidity correlated well with these systems' potencies to induce lipid peroxidation, as detected by conjugated diene formation. Treatment of ER membranes with H2O2 had no effect on fluidity or conjugated diene formation. Using the two most potent free radical generating systems, FeSO4-EDTA and FeSO4-EDTA/hydrogen peroxide, a protective effect of the novel antihypoxic and antiarrhytmic drug stobadine was tested. Stobadine and two well-known antioxidants, alpha-tocopherol acetate and butylated hydroxytoluene, demonstrated the ability to prevent free radical induced alterations in ER membrane fluidity. These results provide new evidence of stobadine's protective effect on membranes attacked by oxygen free radicals.
引用
收藏
页码:815 / 820
页数:6
相关论文
共 44 条
[1]   EFFECTS OF FREE-RADICALS ON THE FLUIDITY OF MYOCARDIAL MEMBRANES [J].
BAGCHI, M ;
PRASAD, MR ;
ENGELMAN, RM ;
DAS, DK .
FREE RADICAL RESEARCH COMMUNICATIONS, 1989, 7 (3-6) :375-380
[2]   HYDROGEN-PEROXIDE ALTERS THE PHYSICAL STATE AND FUNCTION OF THE PLASMA-MEMBRANE OF PULMONARY-ARTERY ENDOTHELIAL-CELLS [J].
BLOCK, ER .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 146 (03) :362-369
[3]  
BRAUGHLER JM, 1986, J BIOL CHEM, V261, P282
[4]   EFFECTS OF IRON-INDUCED LIPID-PEROXIDATION AND OF ACIDOSIS ON CHOLINE UPTAKE BY SYNAPTOSOMES [J].
CANCELA, JM ;
BRALET, J ;
BELEY, A .
NEUROCHEMICAL RESEARCH, 1994, 19 (07) :833-837
[5]   EFFECT OF HYDROXYL RADICAL ON NA+-K+-ATPASE ACTIVITY OF THE BRAIN MICROSOMAL-MEMBRANES [J].
CHEN, JW ;
ZHANG, LP ;
LIAN, XF ;
FEN, H .
CELL BIOLOGY INTERNATIONAL REPORTS, 1992, 16 (09) :927-936
[6]   LIPID-PEROXIDATION INCREASES THE MOLECULAR ORDER OF MICROSOMAL-MEMBRANES [J].
CURTIS, MT ;
GILFOR, D ;
FARBER, JL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1984, 235 (02) :644-649
[7]   LIPID-PEROXIDATION IN SARCOPLASMIC-RETICULUM MEMBRANES - EFFECT ON FUNCTIONAL AND BIOPHYSICAL PROPERTIES [J].
DINIS, TCP ;
ALMEIDA, LM ;
MADEIRA, VMC .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 301 (02) :256-264
[8]  
EDELMAN AM, 1985, J NEUROSCI, V5, P2609
[9]   MICROSOMAL LIPID-PEROXIDATION CAUSES AN INCREASE IN THE ORDER OF THE MEMBRANE LIPID DOMAIN [J].
EICHENBERGER, K ;
BOHNI, P ;
WINTERHALTER, KH ;
KAWATO, S ;
RICHTER, C .
FEBS LETTERS, 1982, 142 (01) :59-62
[10]   IRON ASCORBATE-INDUCED LIPID-PEROXIDATION CHANGES MEMBRANE FLUIDITY AND MUSCARINIC CHOLINERGIC RECEPTOR-BINDING IN RAT FRONTAL-CORTEX [J].
GHOSH, C ;
DICK, RM ;
ALI, SF .
NEUROCHEMISTRY INTERNATIONAL, 1993, 23 (05) :479-484