Abnormalities in the mitochondrial permeability transition in diabetic rats

被引:24
作者
Kristal, BS [1 ]
Matsuda, M [1 ]
Yu, BP [1 ]
机构
[1] UNIV TEXAS,HLTH SCI CTR,DEPT MED,DIV DIABET,SAN ANTONIO,TX 78284
关键词
D O I
10.1006/bbrc.1996.0776
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
Evidence of mitochondrial dysfunction in diabetes led us to examine whether diabetes altered the nature of the mitochondrial permeability transition. Our data reveal three diabetes-associated abnormalities in PT function: consistently delayed induction with calcium-phosphate, a variable delay with calcium-t-butyl-hydroperoxide (t-BuOOH), and an enhanced magnitude of response. The consistently delayed induction in calcium and phosphate is correlated with serum glucose levels, and is consistent with known changes in calcium uniporter function in diabetics. These data expand our knowledge of diabetes-associated abnormalities in mitochondrial function, represent the first evidence that the PT is altered by chronic disease, and provide potential partial mechanistic explanations for the previously observed resistance of diabetic tissues to ischemia-reperfusion injury and the altered Ca2+ homeostasis in diabetics. (C) 1996 Academic Press, Inc.
引用
收藏
页码:519 / 523
页数:5
相关论文
共 30 条
[1]   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
[2]   PERMEABILITY OF INNER MITOCHONDRIAL-MEMBRANE AND OXIDATIVE STRESS [J].
CARBONERA, D ;
AZZONE, GF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 943 (02) :245-255
[3]   PERMEABILIZATION OF THE INNER MITOCHONDRIAL-MEMBRANE BY CA2+ IONS IS STIMULATED BY T-BUTYL HYDROPEROXIDE AND MEDIATED BY REACTIVE OXYGEN SPECIES GENERATED BY MITOCHONDRIA [J].
CASTILHO, RF ;
KOWALTOWSKI, AJ ;
MEINICKE, AR ;
BECHARA, EJH ;
VERCESI, AE .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (03) :479-486
[4]   RECRUITMENT OF MITOCHONDRIAL CYCLOPHILIN TO THE MITOCHONDRIAL INNER MEMBRANE UNDER CONDITIONS OF OXIDATIVE STRESS THAT ENHANCE THE OPENING OF A CALCIUM-SENSITIVE NONSPECIFIC CHANNEL [J].
CONNERN, CP ;
HALESTRAP, AP .
BIOCHEMICAL JOURNAL, 1994, 302 :321-324
[5]   EVIDENCE FOR THE PRESENCE OF A REVERSIBLE CA-2+-DEPENDENT PORE ACTIVATED BY OXIDATIVE STRESS IN HEART-MITOCHONDRIA [J].
CROMPTON, M ;
COSTI, A ;
HAYAT, L .
BIOCHEMICAL JOURNAL, 1987, 245 (03) :915-918
[6]  
DHALLA NS, 1993, CAN J CARDIOL, V9, P873
[7]   ON THE INVOLVEMENT OF A CYCLOSPORINE-A SENSITIVE MITOCHONDRIAL PORE IN MYOCARDIAL REPERFUSION INJURY [J].
DUCHEN, MR ;
MCGUINNESS, O ;
BROWN, LA ;
CROMPTON, M .
CARDIOVASCULAR RESEARCH, 1993, 27 (10) :1790-1794
[8]   EFFECTS OF ISCHEMIA ON RAT MYOCARDIAL-FUNCTION AND METABOLISM IN DIABETES [J].
FEUVRAY, D ;
IDELLWENGER, JA ;
NEELY, JR .
CIRCULATION RESEARCH, 1979, 44 (03) :322-329
[9]   FURTHER EVIDENCE THAT CYCLOSPORINE-A PROTECTS MITOCHONDRIA FROM CALCIUM OVERLOAD BY INHIBITING A MATRIX PEPTIDYL-PROLYL CIS-TRANS ISOMERASE - IMPLICATIONS FOR THE IMMUNOSUPPRESSIVE AND TOXIC EFFECTS OF CYCLOSPORINE [J].
GRIFFITHS, EJ ;
HALESTRAP, AP .
BIOCHEMICAL JOURNAL, 1991, 274 :611-614
[10]  
GRINBLAT L, 1988, BIOCHEM INT, V17, P329