Limited exercise capacity in heterozygous manganese superoxide dismutase gene-knockout mice - Roles of superoxide anion and nitric oxide

被引:48
作者
Kinugawa, S [1 ]
Wang, ZP [1 ]
Kaminski, PM [1 ]
Wolin, MS [1 ]
Edwards, JG [1 ]
Kaley, G [1 ]
Hintze, TH [1 ]
机构
[1] New York Med Coll, Dept Physiol, Valhalla, NY 10595 USA
关键词
nitric oxide; endothelium-derived factors; exercise; free radicals; metabolism;
D O I
10.1161/01.CIR.0000159261.11520.63
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - We have reported that there is a limitation of exercise capacity in mice with defects in the expression of endothelial nitric oxide ( NO) synthase, which is associated with a greater increase in whole-body oxygen consumption ((V) over dot O-2). We hypothesized that in states in which superoxide anion (O-2(-)) is increased, especially in the mitochondria, whole-body (V) over dot O-2 will be increased because of the inactivation of NO, and consequently, exercise capacity will be reduced. Methods and Results - Heterozygous manganese superoxide anion dismutase ( SOD2) gene - knockout mice ( SOD2(+/-)), in which SOD2 activity is reduced by 30% to 80%, and wild-type control mice (SOD2(+/+)) were treadmill-tested to measure indices defining exercise capacity. Tempol was given to each mouse for 7 days by an intraperitoneal injection to scavenge O-2(-) before a second treadmill testing. (V) over dot O-2 and carbon dioxide production ((V) over dot CO2) at rest were increased in SOD2(+/-). The work ( vertical distance run x body weight) to exhaustion was decreased in SOD2(+/-). When the maximum (V) over dot O-2 and (V) over dot CO2 were corrected to per work unit, they were increased in SOD2(+/-). Tempol normalized basal (V) over dot O-2 and (V) over dot CO2 and improved the work to exhaustion and corrected (V) over dot O-2 and (V) over dot CO2 in SOD2(+/-). (V) over dot O-2 of skeletal muscle was measured in vitro. Bradykinin-induced reduction in (V) over dot O-2 in vitro was attenuated in SOD2(+/-), and was acutely restored by Tempol. There was a decrease in SOD2 protein level and a concomitant increase in lucigenin-detectable O-2(-) production in skeletal muscle from SOD2(+/-). Conclusions - These results suggest that exercise capacity is reduced in conditions in which superoxide anion is increased, and this is associated with a greater increase in whole-body oxygen consumption in SOD2(+/-) compared with SOD2(+/+).
引用
收藏
页码:1480 / 1486
页数:7
相关论文
共 40 条
[1]   NAD(P)H oxidase-generated superoxide anion accounts for reduced control of myocardial O2 consumption by NO in old Fischer 344 rats [J].
Adler, A ;
Messina, E ;
Sherman, B ;
Wang, ZP ;
Huang, H ;
Linke, A ;
Hintze, TH .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (03) :H1015-H1022
[2]   Function and production of nitric oxide in the coronary circulation of the conscious dog during exercise [J].
Bernstein, RD ;
Ochoa, FY ;
Xu, XB ;
Forfia, P ;
Shen, WQ ;
Thompson, CI ;
Hintze, TH .
CIRCULATION RESEARCH, 1996, 79 (04) :840-848
[3]   REVERSIBLE INHIBITION OF CYTOCHROME-C-OXIDASE, THE TERMINAL ENZYME OF THE MITOCHONDRIAL RESPIRATORY-CHAIN, BY NITRIC-OXIDE - IMPLICATIONS FOR NEURODEGENERATIVE DISEASES [J].
CLEETER, MWJ ;
COOPER, JM ;
DARLEYUSMAR, VM ;
MONCADA, S ;
SCHAPIRA, AHV .
FEBS LETTERS, 1994, 345 (01) :50-54
[4]   FREE-RADICALS AND TISSUE-DAMAGE PRODUCED BY EXERCISE [J].
DAVIES, KJA ;
QUINTANILHA, AT ;
BROOKS, GA ;
PACKER, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 107 (04) :1198-1205
[5]  
De Sousa E, 2000, CIRCULATION, V102, P1847
[6]   MURINE CYTOTOXIC ACTIVATED MACROPHAGES INHIBIT ACONITASE IN TUMOR-CELLS - INHIBITION INVOLVES THE IRON-SULFUR PROSTHETIC GROUP AND IS REVERSIBLE [J].
DRAPIER, JC ;
HIBBS, JB .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (03) :790-797
[7]   VITAMIN-E-DEFICIENCY AND VITAMIN-C SUPPLEMENTS - EXERCISE AND MITOCHONDRIAL OXIDATION [J].
GOHIL, K ;
PACKER, L ;
DELUMEN, B ;
BROOKS, GA ;
TERBLANCHE, SE .
JOURNAL OF APPLIED PHYSIOLOGY, 1986, 60 (06) :1986-1991
[8]   SITES OF INHIBITION OF MITOCHONDRIAL ELECTRON-TRANSPORT IN MACROPHAGE-INJURED NEOPLASTIC-CELLS [J].
GRANGER, DL ;
LEHNINGER, AL .
JOURNAL OF CELL BIOLOGY, 1982, 95 (02) :527-535
[9]   SUPEROXIDE ANION IS INVOLVED IN THE BREAKDOWN OF ENDOTHELIUM-DERIVED VASCULAR RELAXING FACTOR [J].
GRYGLEWSKI, RJ ;
PALMER, RMJ ;
MONCADA, S .
NATURE, 1986, 320 (6061) :454-456
[10]   EFFECTS OF NO SYNTHASE INHIBITION ON THE MUSCULAR BLOOD-FLOW RESPONSE TO TREADMILL EXERCISE IN RATS [J].
HIRAI, T ;
VISNESKI, MD ;
KEARNS, KJ ;
ZELIS, R ;
MUSCH, TI .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (03) :1288-1293