The mitochondrial membrane permeability transition induced by inorganic phosphate or inorganic arsenate. A comparative study

被引:17
作者
Bravo, C [1 ]
Chavez, E [1 ]
Rodriguez, JS [1 ]
MorenoSanchez, R [1 ]
机构
[1] INST NACL CARDIOL,DEPT BIOQUIM,MEXICO CITY 14080,DF,MEXICO
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY | 1997年 / 117卷 / 01期
关键词
mitochondria; membrane permeability transition; membrane potential; adenine nucleotide translocase; calcium; inorganic phosphate; inorganic arsenate; ADP; cyclosporin A; carboxyatractolyside;
D O I
10.1016/S0305-0491(96)00257-X
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 membrane permeability transition (MPT) induced by Ca2+ and Pi or Asi was studied in rat kidney mitochondria. Membrane potential, Ca2+ transport and swelling were used to monitor the MPT. Asi promoted a faster and more extensive collapse of membrane potential, Ca2+ release and swelling than Pi. The MPT induced by Pi was fully blocked by Mg2+ + ADP, spermine + ADP, Mg2+ + cyclosporin A (CSA), and ADP + CSA. In contrast, the MPT induced by Asi was only prevented, although not completely, by CSA + Mg2+ Or ADP + CSA. Asi, but not Pi, was able to cause collapse of membrane potential in the presence of Sr2+. Carboxyatractyloside (CAT) produced collapse of membrane potential at a lower concentration in the presence of Asi + Ca2+ + ADP than with Pi + Ca2+ + ADP. The addition of Pi + Ca2+ to [C-14]-ADP loaded mitochondria brought about a greater ADP release than Asi + Ca2+. The ADP release was CAT sensitive with Pi, but it was only partially blocked by Asi. The diminution of external pH did not inhibit the MPT induced by Pi or Asi. The results of this study suggest that the adenine nucleotide translocase does not have an essential role in the MPT induced by Asi + Ca2+. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:93 / 99
页数:7
相关论文
共 42 条
[1]   SAFRANINE AS A PROBE OF MITOCHONDRIAL-MEMBRANE POTENTIAL [J].
AKERMAN, KEO ;
WIKSTROM, MKF .
FEBS LETTERS, 1976, 68 (02) :191-197
[2]   AN ADP-SENSITIVE CYCLOSPORINE-A-BINDING PROTEIN IN RAT-LIVER MITOCHONDRIA [J].
ANDREEVA, L ;
CROMPTON, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 221 (01) :261-268
[3]   EVIDENCE FOR THE INVOLVEMENT OF A MEMBRANE-ASSOCIATED CYCLOSPORINE-A-BINDING PROTEIN IN THE CA2+-ACTIVATED INNER MEMBRANE PORE OF HEART-MITOCHONDRIA [J].
ANDREEVA, L ;
TANVEER, A ;
CROMPTON, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 230 (03) :1125-1132
[4]  
ANDREYEV AY, 1994, BIOCHEM MOL BIOL INT, V34, P367
[5]  
BROEKEMEIER KM, 1985, J BIOL CHEM, V260, P105
[6]  
BROEKEMEIER KM, 1989, J BIOL CHEM, V264, P7826
[7]  
CHAVEZ E, 1988, J BIOL CHEM, V263, P3582
[8]   INTRAMITOCHONDRIAL K+ AS ACTIVATOR OF CARBOXYATRACTYLOSIDE-INDUCED CA-2+ RELEASE [J].
CHAVEZ, E ;
MORENOSANCHEZ, R ;
ZAZUETA, C ;
REYESVIVAS, H ;
ARTEAGA, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1070 (02) :461-466
[9]   EVIDENCE FOR THE INVOLVEMENT OF DITHIOL GROUPS IN MITOCHONDRIAL CALCIUM-TRANSPORT - STUDIES WITH CADMIUM [J].
CHAVEZ, E ;
BRIONES, R ;
MICHEL, B ;
BRAVO, C ;
JAY, D .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 242 (02) :493-497
[10]   CHARACTERIZATION BY HG-2+ OF 2 DIFFERENT PATHWAYS FOR MITOCHONDRIAL CA-2+ RELEASE [J].
CHAVEZ, E ;
ZAZUETA, C ;
DIAZ, E ;
HOLQUIN, JA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 986 (01) :27-32