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Modulation of (Na,K)-ATPase activity by membrane fatty acid composition: Therapeutic implications in human hypertension

机译:膜脂肪酸成分对(Na,K)-ATPase活性的调节:对人类高血压的治疗意义

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Oxidative stress (OS) plays a key role in the pathophysiology of essential hypertension and is associated with changes in the cell membrane fatty acid composition and fluidity. As (Na,K)-ATPase is modulated by the surrounding lipid microenvironment, lipid peroxidation could alter the interactions of this enzyme with the membrane components. Thus, modifications in the membrane fatty acid profile will translate into effects on (Na,K)-ATPase activity. Accordingly, a decrease in this enzyme activity has been reported in hypertensive patients. The aim of this study was to evaluate the relationship between membrane fluidity and fatty acid composition and (Na,K)-ATPase activity in erythrocytes of essential hypertensive patients supplemented with antioxidant vitamins C and E. A double-blind, randomized, placebo-controlled study was conducted in 120 men with essential hypertension assigned to receive vitamin C (1 g/day) + E (400 IU/day) or placebo for 8 weeks. Measurements included OS related parameters: GSH/GSSG ratio, F2-isoprostanes and antioxidant capacity of plasma, (Na,K)-ATPase activity and erythrocytes membrane fatty acid composition (PUFA, polyunsaturated fatty acids; SAFA, saturated fatty acids). Associations were assessed by Pearson correlation and the differences by Student t-test (p < 0.05). Supplemented hypertensive patients showed higher activity of (Na,K)-ATPase and proportion of PUFA, and lower blood pressure, OS markers and proportion of SAFA, versus placebo. The activity of (Na,K)-ATPase correlated negatively with the proportion of SAFA, but positively with that of PUFA in both groups. Supplementation with vitamins C + E resulted in decreased OS and increased fluidity and PUFA proportion in the membrane, both of which positively modulate (Na,K)-ATPase activity, accounting for the blood pressure reduction.
机译:氧化应激(OS)在原发性高血压的病理生理中起关键作用,并与细胞膜脂肪酸组成和流动性的变化有关。由于(Na,K)-ATPase受周围脂质微环境调节,脂质过氧化作用可改变该酶与膜成分的相互作用。因此,膜脂肪酸谱的修饰将转化为对(Na,K)-ATPase活性的影响。因此,据报道在高血压患者中该酶活性降低。这项研究的目的是评估补充抗氧化剂维生素C和E的原发性高血压患者的膜流动性和脂肪酸组成与红细胞中(Na,K)-ATPase活性之间的关系。双盲,随机,安慰剂对照该研究在120名患有原发性高血压的男性中进行,他们接受了8周的维生素C(1克/天)+ E(400 IU /天)或安慰剂的治疗。测量包括与OS相关的参数:GSH / GSSG比,血浆中的F2-异前列腺素和抗氧化能力,(Na,K)-ATPase活性和红细胞膜脂肪酸组成(PUFA,多不饱和脂肪酸; SAFA,饱和脂肪酸)。通过皮尔森相关性评估关联,通过学生t检验评估差异(p <0.05)。与安慰剂相比,补充性高血压患者表现出较高的(Na,K)-ATPase活性和PUFA比例,并且血压,OS标记物和SAFA比例较低。两组中(Na,K)-ATPase的活性与SAFA的含量呈负相关,与PUFA的含量呈正相关。补充维生素C + E会导致OS降低以及膜中的流动性和PUFA比例增加,这两者均能正向调节(Na,K)-ATPase活性,从而降低了血压。

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