Free radical scavenging action of the natural polyamine spermine in rat liver mitochondria

被引:83
作者
Sava, Irina G. [1 ]
Battaglia, Valentina [1 ]
Rossi, Carlo A. [1 ]
Salvi, Mauro [1 ]
Toninello, Antonio [1 ]
机构
[1] Univ Padua, Dipartimento Chim Biol, Ist Neurosci, Unita Studio Biomembrane,CNR, I-35121 Padua, Italy
关键词
mitochondria; spermine; hydroxyl radical; oxidative stress; mitochondrial permeability transition; free radicals;
D O I
10.1016/j.freeradbiomed.2006.07.008
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 isoflavonoid genistein, the cyclic triterpene glycyrrhetinic acid, and salicylate induce mitochondrial swelling and loss of membrane potential (Delta Psi) in rat liver mitochondria (RLM). These effects are Ca2+-dependent and are prevented by cyclosporin A and bongkrekik acid, classic inhibitors of mitochondrial permeability transition (MPT). This membrane permeabilization is also inhibited by N-ethylmaleimide, butylhydroxytoluene, and mannitol. The above-mentioned pro-oxidants also induce an increase in O-2 consumption and H2O2 generation and the oxidation of sulfhydryl groups, glutathione, and pyridine nucleotides. All these observations are indicative of the induction of MPT mediated by oxidative stress. At concentrations similar to those present in the cell, spermine can prevent swelling and Delta Psi collapse, that is, MPT induction. Spermine, by acting as a free radical scavenger, in the absence of Ca2+ inhibits H2O2 production and maintains glutathione and sulfhydryl groups at normal reduced level, so that the critical thiols responsible for pore opening are also consequently prevented from being oxidized. Spermine also protects RLM under conditions of accentuated thiol and glutathione oxidation, lipid peroxidation, and protein oxidation, suggesting that its action takes place by scavenging the hydroxyl radical. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1272 / 1281
页数:10
相关论文
共 40 条
[21]   Protein tyrosine phosphatases in signal transduction [J].
Neel, BG ;
Tonks, NK .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (02) :193-204
[22]   The role of creatine kinase in inhibition of mitochondrial permeability transition [J].
OGorman, E ;
Beutner, G ;
Dolder, M ;
Koretsky, AP ;
Brdiczka, D ;
Wallimann, T .
FEBS LETTERS, 1997, 414 (02) :253-257
[23]   GLUTATHIONE - TOXICOLOGICAL IMPLICATIONS [J].
REED, DJ .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1990, 30 :603-631
[24]  
REZNICK AZ, 1994, METHOD ENZYMOL, V233, P357
[25]   EFFECT OF SPERMINE ON MITOCHONDRIAL GLUTATHIONE RELEASE [J].
RIGOBELLO, MP ;
TONINELLO, A ;
SILIPRANDI, D ;
BINDOLI, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 194 (03) :1276-1281
[26]   Interaction of genistein with the mitochondrial electron transport chain results in opening of the membrane transition pore [J].
Salvi, M ;
Brunati, AM ;
Clari, G ;
Toninello, A .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2002, 1556 (2-3) :187-196
[27]   Effect of naturally occurring flavonoids on lipid peroxidation and membrane permeability transition in mitochondria [J].
Santos, AC ;
Uyemura, SA ;
Lopes, JLC ;
Bazon, JN ;
Mingatto, FE ;
Curti, C .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (09) :1455-1461
[28]   CALCIUM-DEPENDENT AND PHOSPHATE-DEPENDENT RELEASE AND LOADING OF GLUTATHIONE BY LIVER-MITOCHONDRIA [J].
SAVAGE, MK ;
JONES, DP ;
REED, DJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1991, 290 (01) :51-56
[29]  
SCHUBER F, 1989, BIOCHEM J, V260, P1
[30]  
Susin SA, 1998, BIOCHIM BIOPHYS ACTA, V194, P1276