Kitson Alex P, Stroud Chad K, Stark Ken D
Laboratory of Nutritional and Nutraceutical Research, Department of Kinesiology, University of Waterloo, Waterloo, ON, N2L 3G1, Canada.
Lipids. 2010 Mar;45(3):209-24. doi: 10.1007/s11745-010-3391-6. Epub 2010 Feb 12.
Observational evidence suggests that in populations consuming low levels of n-3 highly unsaturated fatty acids, women have higher blood levels of docosahexaenoic acid (DHA; 22:3n-6) as compared with men. Increased conversion of alpha-linolenic acid (ALA; 18:3n-3) to DHA by females has been confirmed in fatty acid stable isotope studies. This difference in conversion appears to be associated with estrogen and some evidence indicates that the expression of enzymes involved in synthesis of DHA from ALA, including desaturases and elongases, is elevated in females. An estrogen-associated effect may be mediated by peroxisome proliferator activated receptor-alpha (PPARalpha), as activation of this nuclear receptor increases the expression of these enzymes. However, because estrogens are weak ligands for PPARalpha, estrogen-mediated increases in PPARalpha activity likely occur through an indirect mechanism involving membrane-bound estrogen receptors and estrogen-sensitive G-proteins. The protein kinases activated by these receptors phosphorylate and increase the activity of PPARalpha, as well as phospholipase A(2) and cyclooxygenase 2 that increase the intracellular concentration of PPARalpha ligands. This review will outline current knowledge regarding elevated DHA production in females, as well as highlight interactions between estrogen signaling and PPARalpha activity that may mediate this effect.
观察性证据表明,在摄入低水平n-3高度不饱和脂肪酸的人群中,与男性相比,女性血液中的二十二碳六烯酸(DHA;22:6n-3)水平更高。脂肪酸稳定同位素研究已证实,女性将α-亚麻酸(ALA;18:3n-3)转化为DHA的能力增强。这种转化差异似乎与雌激素有关,一些证据表明,参与从ALA合成DHA的酶(包括去饱和酶和延长酶)在女性中的表达升高。雌激素相关效应可能由过氧化物酶体增殖物激活受体α(PPARα)介导,因为该核受体的激活会增加这些酶的表达。然而,由于雌激素是PPARα的弱配体,雌激素介导的PPARα活性增加可能通过涉及膜结合雌激素受体和雌激素敏感G蛋白的间接机制发生。这些受体激活的蛋白激酶使PPARα磷酸化并增加其活性,以及增加PPARα配体细胞内浓度的磷脂酶A2和环氧化酶2。本综述将概述目前关于女性DHA产量升高的知识,并强调雌激素信号与PPARα活性之间可能介导这种效应的相互作用。