Effects of methionine on endogenous antioxidants in the heart

被引:26
作者
Seneviratne, CK
Li, TM
Khaper, N
Singal, PK
机构
[1] St Boniface Gen Hosp, Res Ctr, Inst Cardiovasc Sci, Winnipeg, MB R2H 2A6, Canada
[2] Univ Manitoba, Fac Med, Dept Physiol, Winnipeg, MB R2H 2A6, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1999年 / 277卷 / 06期
关键词
lipid peroxidation; gene expression;
D O I
10.1152/ajpheart.1999.277.6.H2124
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The deficiency of methionine, an essential amino acid, is associated with cardiovascular lesions. Because different types of cardiac pathologies are caused by a decrease in antioxidants, we examined the effects of methionine on myocardial antioxidant enzymes in hemodynamically assessed rats that were treated with methionine (10 mg/ml) in drinking water for 12, 24, and 48 h. Glutathione peroxidase (GSHPx) activity was significantly increased to 150.5 +/- 12.2 and 191.7 +/- 13.7% of the control value at 12 and 24 h, respectively, followed by a decline to 120 +/- 24.6% at 48 h. The mRNA levels of GSHPx at these time points were 151.2 +/- 12.0, 218.7 +/- 35.3, and 173.5 +/- 25.2%, respectively. Superoxide dismutase (SOD) activity was 144.3 +/- 3.7, 114.3 +/- 10.1, and 143.1 +/- 11.2% at 12, 24, and 48 h, respectively. Catalase (Cat) activity was 272.4 +/- 5.4, 237.8 +/- 16.6, and 224.1 +/- 17.3% of the control value. The expression of Cat and SOD mRNA was unchanged at 12, 24, and 48 h. The lipid peroxidation was decreased by 24.4 +/- 11.2, 54.9 +/- 0.1, and 6.4 +/- 2.1% at 12, 24, and 48 h, respectively. Methionine had no effect on the ventricular or aortic pressures, heart rate, and myocardial glutathione levels at any of the time points. The study shows that methionine has a significant effect on the myocardial antioxidant enzyme activities, and only changes in GSHPx enzyme activity correlated with the mRNA changes. These antioxidant changes may have a role in the beneficial effects of methionine in pathological rather than physiological conditions.
引用
收藏
页码:H2124 / H2128
页数:5
相关论文
共 40 条
[1]  
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[2]  
Aust SD., 1985, Handbook of methods for oxygen radical research, V1, P203
[4]   THE CLINICAL POTENTIAL OF ADEMETIONINE (S-ADENOSYLMETHIONINE) IN NEUROLOGICAL DISORDERS [J].
BOTTIGLIERI, T ;
HYLAND, K ;
REYNOLDS, EH .
DRUGS, 1994, 48 (02) :137-152
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]  
CLAIRBORNE A, 1985, HDB METHODS OXYGEN R, P253
[7]   THE REGULATION OF GLUTATHIONE-PEROXIDASE GENE-EXPRESSION BY OXYGEN-TENSION IN CULTURED HUMAN CARDIOMYOCYTES [J].
COWAN, DB ;
WEISEL, RD ;
WILLIAMS, WG ;
MICKLE, DAG .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1992, 24 (04) :423-433
[8]   ENZYMATIC DEFENSES OF THE MOUSE HEART AGAINST REACTIVE OXYGEN METABOLITES - ALTERATIONS PRODUCED BY DOXORUBICIN [J].
DOROSHOW, JH ;
LOCKER, GY ;
MYERS, CE .
JOURNAL OF CLINICAL INVESTIGATION, 1980, 65 (01) :128-135
[9]   PREGNANCY-RELATED MODIFICATIONS OF RAT MYOMETRIAL GS PROTEINS - ADP-RIBOSYLATION, IMMUNOREACTIVITY AND GENE-EXPRESSION STUDIES [J].
ELWARDYMEREZAK, J ;
MALTIER, JP ;
COHEN-TANNOUDJI, J ;
LECRIVAIN, JL ;
VIVAT, V ;
LEGRAND, C .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1994, 13 (01) :23-37
[10]  
GLADININ MT, 1980, J NUTR, V110, P1197