蛋氨酸对心脏内源性抗氧化剂的影响。

C K Seneviratne, T Li, N Khaper, P K Singal
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引用次数: 25

摘要

蛋氨酸(一种必需氨基酸)的缺乏与心血管疾病有关。由于不同类型的心脏疾病是由抗氧化剂的减少引起的,我们研究了蛋氨酸对血液动力学评估大鼠心肌抗氧化酶的影响,蛋氨酸(10 mg/ml)在饮用水中处理12、24和48小时。谷胱甘肽过氧化物酶(GSHPx)活性在12和24小时分别显著增加到对照值的150.5 +/- 12.2和191.7 +/- 13.7%。48 h GSHPx mRNA水平分别为151.2 +/- 12.0、218.7 +/- 35.3和173.5 +/- 25.2%。超氧化物歧化酶(SOD)活性分别为144.3 +/- 3.7、114.3 +/- 10.1和143.1 +/- 11。分别在12、24和48小时添加2%。过氧化氢酶(Cat)活性分别为对照的272.4 +/- 5.4、237.8 +/- 16.6和224.1 +/- 17.3%。在12、24和48 h时,Cat和SOD mRNA的表达没有变化,脂质过氧化降低了24.4 +/- 11.2,54。在12、24和48 h分别为9 +/- 0.1和6.4 +/- 2.1%。蛋氨酸在任何时间点对心室或主动脉压、心率和心肌谷胱甘肽水平均无影响。研究表明,蛋氨酸对心肌抗氧化酶活性有显著影响,且只有GSHPx酶活性的变化与mRNA的变化相关。这些抗氧化的变化可能在病理而非生理条件下蛋氨酸的有益作用中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of methionine on endogenous antioxidants in the heart.

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.

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