Modulatory effect of cyclosporin A on tert-butyl hydroperoxide-induced oxidative damage in hepatocytes

被引:12
作者
Kmonícková, E
Drahota, Z
Kameníková, L
Cervinková, Z
Masek, K
Farghali, H
机构
[1] Charles Univ Prague, Inst Pharmacol, Fac Med 1, Prague 12800 2, Czech Republic
[2] Acad Sci Czech Republ, Inst Physiol, CR-14220 Prague 4, Czech Republic
[3] Acad Sci Czech Republ, Inst Pharmacol, Prague 14220, Czech Republic
[4] Charles Univ Prague, Fac Med, Dept Physiol, Hradec Kralove 50001, Czech Republic
关键词
D O I
10.1081/IPH-100102566
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
In the present work, we followed an in vitro protective action of cyclosporin A (CsA) against tert-butyl hydroperoxide (t-BHP)-induced oxidative damage in hepatocytes. Various parameters (cell viability, cytosolic calcium Level, rhodamine 123 accumulation as indicator of mitochondrial membrane potential and alanine-aminotransferase leakage from cells) were measured as an index of cytotoxicity. Tert-butyl hydroperoxide (1 mM) significantly increased cytosolic Ca2+ and affected mitochondrial membrane potential. Pretreatment with cyclosporin A (0.5 muM) reduced t-BHP-induced cytosolic Ca2+ increase and ALT (alanine-aminotransferase) leakage, but had no protective effect on t-BHP-induced changes of mitochondrial membrane potential. Our data thus suggest that the mechanism of cytoprotection of CsA on the cytosolic Ca2+ changes and ALT leakage induced by t-BHP, does not directly correlate with protection of t-BHP-induced changes of mitochondrial membrane potential.
引用
收藏
页码:43 / 54
页数:12
相关论文
共 31 条
[1]
PYRIDINE-NUCLEOTIDE OXIDATION, CA-2+ CYCLING AND MEMBRANE DAMAGE DURING TERT-BUTYL HYDROPEROXIDE METABOLISM BY RAT-LIVER MITOCHONDRIA [J].
BELLOMO, G ;
MARTINO, A ;
RICHELMI, P ;
MOORE, GA ;
JEWELL, SA ;
ORRENIUS, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 140 (01) :1-6
[2]
RECENT PROGRESS ON REGULATION OF THE MITOCHONDRIAL PERMEABILITY TRANSITION PORE - A CYCLOSPORINE-SENSITIVE PORE IN THE INNER MITOCHONDRIAL-MEMBRANE [J].
BERNARDI, P ;
BROEKEMEIER, KM ;
PFEIFFER, DR .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1994, 26 (05) :509-517
[3]
BLACKMORE PF, 1985, METHOD ENZYMOL, V109, P550
[4]
CYCLOSPORINE-A PROTECTS HEPATOCYTES SUBJECTED TO HIGH CA-2+ AND OXIDATIVE STRESS [J].
BROEKEMEIER, KM ;
CARPENTERDEYO, L ;
REED, DJ ;
PFEIFFER, DR .
FEBS LETTERS, 1992, 304 (2-3) :192-194
[5]
Inhibition of the mitochondrial permeability transition by cyclosporin a during long time frame experiments: Relationship between pore opening and the activity of mitochondrial phospholipases [J].
Broekemeier, KM ;
Pfeiffer, DR .
BIOCHEMISTRY, 1995, 34 (50) :16440-16449
[6]
Cyclosporin A induces a biphasic increase in KCl-induced calcium influx in GH3 pituitary cells [J].
Chou, YC ;
Fong, JC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (01) :169-173
[7]
RHODAMINE-123 AS A PROBE OF TRANSMEMBRANE POTENTIAL IN ISOLATED RAT-LIVER MITOCHONDRIA - SPECTRAL AND METABOLIC PROPERTIES [J].
EMAUS, RK ;
GRUNWALD, R ;
LEMASTERS, JJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 850 (03) :436-448
[8]
FARGHALI H, 1994, PHYSIOL RES, V43, P121
[9]
Immunopharmacologic agents in the amelioration of hepatic injuries [J].
Farghali, H ;
Masek, K .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1998, 20 (4-5) :125-139
[10]
MECHANISMS BY WHICH MITOCHONDRIA TRANSPORT CALCIUM [J].
GUNTER, TE ;
PFEIFFER, DR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (05) :C755-C786