首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Effects of eicosapentaenoic acid on blood pressure, cell membrane fatty acids, and intracellular sodium concentration in essential hypertension.
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Effects of eicosapentaenoic acid on blood pressure, cell membrane fatty acids, and intracellular sodium concentration in essential hypertension.

机译:二十碳五烯酸对原发性高血压患者的血压,细胞膜脂肪酸和细胞内钠浓度的影响。

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摘要

This study was designed to clarify the effects of orally administered eicosapentaenoic acid (EPA) on blood pressure, intracellular sodium content, and cell membrane fatty acid composition in patients with essential hypertension. After a 4-week run-in period, a study group of 17 male patients was assigned to an 8-week treatment with EPA (2.7 g/day) or placebo in a randomized, double-blind fashion with a crossover at week 4. Systolic blood pressure (SBP) was lower after treatment with EPA than after treatment with placebo (152.9+/-17.3 vs. 162.6+/-20.6 mmHg; p<0.01), while diastolic blood pressure was not statistically different. Compared with the placebo treatment, EPA supplementation resulted in a decrease in intraerythrocyte sodium content (R-Na; 11.17+/-0.63 vs. 10.44+/-1.28 nmol/l cells; p<0.05) accompanied by an increase (p<0.001) in erythrocyte membrane EPA content. The increase in membrane EPA content was related to the decrease in SBP (r=-0.52, p<0.05) and the decrease in R-Na (r=-0.57, p<0.02) during EPA treatment. The decrease in R-Na correlated positively with the decrease in SBP (r=0.54, p<0.05), and correlated negatively with the change in Na+-K+ ATPase activity (r= -0.59, p<0.02). However, the change in Na+-K+ ATPase activity did not directly correlate with the change in membrane EPA content. In conclusion, oral EPA supplementation increased membrane EPA content and reduced SBP in patients with essential hypertension. Based on the association between the increase in membrane EPA content and the decrease in intracellular sodium concentration, EPA may lower blood pressure by altering the activities of the membrane sodium transport systems.
机译:本研究旨在阐明口服二十碳五烯酸(EPA)对原发性高血压患者血压,细胞内钠含量和细胞膜脂肪酸组成的影响。经过4周的磨合期后,一个研究小组的17名男性患者被分配到以EPA(2.7 g /天)或安慰剂进行为期8周的治疗,以随机,双盲的方式进行,并在第4周进行转换。 EPA治疗后的收缩压(SBP)低于安慰剂治疗后的收缩压(152.9 +/- 17.3 vs. 162.6 +/- 20.6 mmHg; p <0.01),而舒张压没有统计学差异。与安慰剂治疗相比,补充EPA导致红细胞内钠含量降低(R-Na; 11.17 +/- 0.63 vs. 10.44 +/- 1.28 nmol / l细胞; p <0.05),同时增加(p <0.001) )红细胞膜中EPA含量。膜EPA含量的增加与EPA处理期间SBP的降低(r = -0.52,p <0.05)和R-Na的降低(r = -0.57,p <0.02)有关。 R-Na的降低与SBP的降低呈正相关(r = 0.54,p <0.05),而与Na + -K + ATPase活性的变化呈负相关(r = -0.59,p <0.02)。但是,Na + -K + ATPase活性的变化与膜EPA含量的变化并不直接相关。总之,口服EPA补充剂可增加原发性高血压患者的膜EPA含量并降低SBP。基于膜EPA含量增加与细胞内钠浓度降低之间的关联,EPA可能会通过改变膜钠转运系统的活性来降低血压。

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