地高辛、咖啡因或异丙肾上腺素预处理大鼠心肌细胞质中的蛋白质氨基酸。

Janusz Gabrys, Janusz Konecki, Maria Głowacka, Katarzyna Durczok, Przemysław Nowak, Grzegorz Bielaczyc, Ryszard Brus, Jashovam Shani
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引用次数: 1

摘要

采用气液色谱法测定了大鼠心房肌和心室肌细胞细胞质中19种蛋白质氨基酸和总游离氨基酸的含量。在大鼠暴露于具有不同作用机制的心脏活性药物地高辛、咖啡因和异丙肾上腺素后,对组织进行分析。我们证明,在对照(未治疗)大鼠心房和心室心肌细胞质中,精氨酸、谷氨酰胺和半胱氨酸的含量最高:35.1%和17.6%;14.8%和51.6%;占游离氨基酸总量的9.9%和0.25%。心房和心室心肌细胞质中其他氨基酸的含量在总游离氨基酸的0.1%至10.0%之间。地高辛、咖啡因和异丙肾上腺素显著降低心房心肌胞质中游离氨基酸的总量,分别为对照组的7.6%、9.0%和9.2%(100%),心室心肌胞质中游离氨基酸的总量分别为对照组的31.1%、43.2%和28.3%。与对照组相比,测试的三种药物改变了心房和心室心肌细胞质中精氨酸、半胱氨酸、色氨酸、天冬酰胺和酪氨酸的水平(以实验组中总游离氨基酸的百分比计算)。本文讨论了蛋白质氨基酸在心肌功能中的作用以及这些药物对哺乳动物心脏的作用机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteinous amino acids in hearts' muscle cytosol of rats pretreated with digoxin, caffeine or isoproterenol.

Levels of the 19 proteinous amino acids and total free amino acids were assayed by gas-liquid chromatography in cytosols of rat atrial and ventricular muscle cardiomyocytes. The tissues were assayed after the rats had been exposed to the cardioactive drugs digoxin, caffeine, and isoproterenol, each having different mechanisms of action. We demonstrated that, in the atrial and ventricular cardiac muscle cytosol of control (untreated) rats, arginine, glutamine, and cysteine existed in their highest levels: 35.1% and 17.6%; 14.8% and 51.6%; 9.9% and 0.25% of the total free amino acids, respectively. The levels of the other amino acids in the atrial and ventricular cardiac muscle cytosols ranged between 0.1% and 10.0% of the total free amino acids. Digoxin, caffeine, and isoproterenol significantly reduced the total amount of cytosolic free amino acids in the atrial heart muscle cytosol to 7.6%, 9.0%, and 9.2% of the control value (100%), and in the ventricular heart muscle cytosol to 31.1%, 43.2%, and 28.3% of the control. The three drugs tested changed the cytosols' levels of arginine, cysteine, tryptophane, asparagine, and tyrosine in atrial and ventricular heart muscle cytosol, as compared to the control groups (calculated as a percent of the total free amino acids in the experimental groups). The role of proteinous amino acids in the function of the heart muscle and in the mechanism of action of these drugs on the mammalian heart is discussed.

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