Alteration of mitochondrial function in a model of chronic ischemia in vivo in rat heart

被引:67
作者
Boudina, S
Laclau, MN
Tariosse, L
Daret, D
Gouverneur, G
Bonoron-Adèle, S
Saks, VA
Dos Santos, P
机构
[1] INSERM, U441, F-33600 Pessac, France
[2] Inst Federatif Rech 4, F-33600 Pessac, France
[3] Univ Grenoble 1, Lab Bioenerget, Grenoble 9, France
[4] NICPB, Lab Bioenerget, EE-12618 Tallinn, Estonia
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2002年 / 282卷 / 03期
关键词
contractile function; energy metabolism; mitochondria;
D O I
10.1152/ajpheart.00471.2001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to investigate mitochondrial alterations in an animal model of chronic myocardial ischemia in rats obtained by surgical constriction of the left coronary artery. Resting coronary blood flow was measured using the fluorescent microsphere technique. Contractile function, defined by rate-pressure product, and myocardial oxygen consumption were measured in a Langendorff preparation. The mitochondrial function was evaluated on permeabilized skinned fibers. Three weeks after surgery, ischemic hearts showed a significant decrease in coronary blood flow compared with sham. Hemodynamic measurements showed a significant systolic and diastolic dysfunction. Alterations in mitochondrial function in ischemic hearts were mainly characterized by a significant decrease in the maximal velocity and apparent half-saturation constant for ADP, loss of the stimulatory effect of creatine, and a stimulatory effect of exogenous cytochrome c. These functional alterations were supported by structural alterations characterized by mitochondrial clustering and swelling associated with membrane rupture. We conclude that the alterations in systolic function after chronic ischemia are supported by severe modifications of mitochondrial structure and function.
引用
收藏
页码:H821 / H831
页数:11
相关论文
共 40 条
[11]   Development of the fluorescent microsphere technique for quantifying regional blood flow in small mammals [J].
Deveci, D ;
Egginton, S .
EXPERIMENTAL PHYSIOLOGY, 1999, 84 (04) :615-630
[12]   COMPLETE INHIBITION OF CREATINE-KINASE IN ISOLATED PERFUSED RAT HEARTS [J].
FOSSEL, ET ;
HOEFELER, H .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (01) :E124-E130
[13]   WALL STRESS AND PATTERNS OF HYPERTROPHY IN HUMAN LEFT-VENTRICLE [J].
GROSSMAN, W ;
JONES, D ;
MCLAURIN, LP .
JOURNAL OF CLINICAL INVESTIGATION, 1975, 56 (01) :56-64
[14]   THE RANDOM COLLISION MODEL AND A CRITICAL-ASSESSMENT OF DIFFUSION AND COLLISION IN MITOCHONDRIAL ELECTRON-TRANSPORT [J].
HACKENBROCK, CR ;
CHAZOTTE, B ;
GUPTE, SS .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1986, 18 (05) :331-368
[15]   Apoptosis - Basic mechanisms and implications for cardiovascular disease [J].
Haunstetter, A ;
Izumo, S .
CIRCULATION RESEARCH, 1998, 82 (11) :1111-1129
[16]  
INGWALL JS, 1993, CIRCULATION, V87, P58
[17]   Early alteration of the control of mitochondrial function in myocardial ischemia [J].
Kay, L ;
Saks, VA ;
Rossi, A .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (12) :3399-3411
[18]   Detection of early ischemic damage by analysis of mitochondrial function in skinned fibers [J].
Kay, L ;
Rossi, A ;
Saks, V .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1997, 174 (1-2) :79-85
[19]   Alteration in the control of mitochondrial respiration by outer mitochondrial membrane and creatine during heart preservation [J].
Kay, L ;
Daneshrad, Z ;
Saks, VA ;
Rossi, A .
CARDIOVASCULAR RESEARCH, 1997, 34 (03) :547-556
[20]  
KLINGENBERG M, 1965, S REGULATION METABOL, P180