多囊卵巢综合征妇女补充omega-3多不饱和脂肪酸期间血浆代谢物和葡萄糖稳态的变化

Sidika E. Karakas , Bertrand Perroud , Tobias Kind , Mine Palazoglu , Oliver Fiehn
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引用次数: 42

摘要

鱼油(FO)和亚麻籽油(FLX)都是n-3多不饱和脂肪酸(PUFA)。鱼油含有长链脂肪酸,而鱼油含有必需的n-3 PUFA。我们证明了FO改变了多囊卵巢综合征(PCOS)女性的胰岛素分泌和抵抗,而FLX没有。令人惊讶的是,鱼油的效果与富含n-6 pufa的大豆油(SBO)相似。由于支链(BCAA)和芳香氨基酸(AA)的增加影响胰岛素分泌和抵抗,我们研究了FO、FLX和/或SBO是否影响血浆代谢物,尤其是AA。在这项为期6周的随机、3平行、双盲研究中,54名女性接受了3.5 g/天的FO、FLX或SBO治疗。在51名完成者(每组17名)中,在开始和结束时测量空腹血浆代谢物。与FLX相比,FO和SBO增加了胰岛素反应和抵抗以及几种BCAA和芳香AA。途径分析表明,鱼油的生化影响最大,影响AA的降解和生物合成、胺、多胺的降解以及丙氨酸、甘氨酸、左旋肉碱的生物合成和TCA循环,而FLX仅对丙氨酸的生物合成和l-半胱氨酸的降解影响最小。结论鱼油和SBO对血浆AA的影响与FLX相似,但有显著差异。膳食多聚脂肪酸的主要目标尚不清楚。膳食多聚脂肪酸可能直接影响胰岛素分泌和胰岛素抵抗,间接改变血浆AA。或者,作为一个新的概念,膳食PUFA可能直接影响AA代谢,胰岛素分泌和抵抗的变化可能是次要的。
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Changes in plasma metabolites and glucose homeostasis during omega-3 polyunsaturated fatty acid supplementation in women with polycystic ovary syndrome

Background

Both fish (FO) and flaxseed oils (FLX) are n-3 polyunsaturated fatty acids (PUFA). Fish oil contains long chain while FLX contains essential n-3 PUFA. We demonstrated that FO altered insulin secretion and resistance in polycystic ovary syndrome (PCOS) women but FLX did not. Surprisingly, the effects of FO were similar to those of the n-6 PUFA-rich soybean oil (SBO). Since increased branched chain (BCAA) and aromatic amino acids (AA) affect insulin secretion and resistance, we investigated whether FO, FLX and /or SBO affect plasma metabolites, especially AA.

Methods and findings

In this six-week, randomized, 3-parallel arm, double-blinded study, 54 women received 3.5 g/day FO, FLX or SBO. In 51 completers (17 from each arm), fasting plasma metabolites were measured at the beginning and at the end.

As compared to FLX, FO and SBO increased insulin response and resistance as well as several BCAA and aromatic AA. Pathway analysis indicated that FO exerted the largest biochemical impact, affecting AA degradation and biosynthesis, amine, polyamine degradation and alanine, glycine, l-carnitine biosynthesis and TCA cycle, while FLX had minimal impact affecting only alanine biosynthesis and l-cysteine degradation.

Conclusion

Effects of FO and SBO on plasma AA were similar and differed significantly from those of the FLX. The primary target of dietary PUFA is not known. Dietary PUFA may influence insulin secretion and resistance directly and alter plasma AA indirectly. Alternatively, as a novel concept, dietary PUFA may directly affect AA metabolism and the changes in insulin secretion and resistance may be secondary.

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