Effect of MI-D, a new mesoionic compound, on energy-linked functions of rat liver mitochondria

被引:31
作者
Cadena, SMSC
Carnieri, EGS
Echevarria, A
de Oliveira, MBM
机构
[1] Univ Fed Parana, Dept Bioquim, BR-81531990 Curitiba, Parana, Brazil
[2] Univ Fed Rural Rio de Janeiro, Dept Quim, Rio De Janeiro, Brazil
关键词
mesoionic compound; mitochondrial uncoupling; ATPase;
D O I
10.1016/S0014-5793(98)01427-6
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
MI-D (4-phenyl-5-(4-nitro-cinnamoyl)-1,3,4-thiadiazolium-2-phenylamine chloride), a new mesoionic compound, depressed the phosphorylation efficiency of liver mitochondria as deduced from an accentuated decrease of the respiratory control coefficient and ADP/O ratio, Analysis of segments of the respiratory chain suggested that the MI-D inhibition site is further on than complex I and between complexes II and III. The transmembrane electrical potential (Delta psi) was collapsed dependent on MI-D concentration. ATPase activity mas dramatically increased by MI-D in intact mitochondria, but inhibited in carbonylcyanide p-trifluoromethoxyphenylhydrazone (FCCP)-uncoupled mitochondria. These results suggest that MI-D acts as an uncoupler agent, a property closely related to its structural characteristics. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:46 / 50
页数:5
相关论文
共 36 条
[1]   SAFRANINE AS A PROBE OF MITOCHONDRIAL-MEMBRANE POTENTIAL [J].
AKERMAN, KEO ;
WIKSTROM, MKF .
FEBS LETTERS, 1976, 68 (02) :191-197
[2]   EFFECTS OF PHOSPHATE AND ELECTRON-TRANSPORT ON CARBONYL CYANIDE META-CHLOROPHENYLHYDRAZONE-INDUCED ATPASE OF RAT-LIVER MITOCHONDRIA [J].
BERTINA, RM ;
SLATER, EC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 376 (03) :492-504
[3]  
CHANCE B, 1955, J BIOL CHEM, V217, P383
[4]  
Corell Tim, 1994, Polish Journal of Pharmacology, V46, P553
[5]  
Estabrook R.W., 1967, METHODS ENZYMOL, V10, P41, DOI DOI 10.1016/0076-6879(67)10010-4
[6]   SYNTHESIS OF SYDNONES AND SYDNONE IMINES [J].
GRECO, CV ;
CHENG, CC ;
NYBERG, WH .
JOURNAL OF MEDICINAL & PHARMACEUTICAL CHEMISTRY, 1962, 5 (04) :861-&
[7]  
GRYNBERG N, 1992, ANTICANCER RES, V12, P1025
[8]   Synthesis and in vivo antitumor activity of new heterocyclic derivatives of the 1,3,4-thiadiazolium-2-aminide class [J].
Grynberg, N ;
Santos, AC ;
Echevarria, A .
ANTI-CANCER DRUGS, 1997, 8 (01) :88-91
[9]   UNCOUPLING OF OXIDATIVE-PHOSPHORYLATION [J].
HANSTEIN, WG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 456 (02) :129-148
[10]   INTERACTION OF UNCOUPLERS WITH THE MITOCHONDRIAL-MEMBRANE - IDENTIFICATION OF THE HIGH AFFINITY BINDING-SITE [J].
KATRE, NV ;
WILSON, DF .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1978, 191 (02) :647-656