Seidel Ulrike, Eberhardt Katharina, Wiebel Michelle, Luersen Kai, Ipharraguerre Ignacio R, Haegele Franziska A, Winterhalter Peter, Bosy-Westphal Anja, Schebb Nils Helge, Rimbach Gerald
Institute of Human Nutrition and Food Science, University of Kiel, Kiel, Germany.
Institute of Food Chemistry, TU Braunschweig, Braunschweig, Germany.
Front Nutr. 2024 Apr 4;11:1359958. doi: 10.3389/fnut.2024.1359958. eCollection 2024.
Ahiflower oil from the seeds of is rich in α-linolenic acid (ALA) and stearidonic acid (SDA). ALA and SDA are potential precursor fatty acids for the endogenous synthesis of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which are n3-long chain polyunsaturated fatty acids (n3-LC-PUFAS), in humans. Since taurine, an amino sulfonic acid, is often associated with tissues rich in n3-LC-PUFAS (e.g., in fatty fish, human retina), taurine may play a role in EPA- and DHA-metabolism.
To examine the capacity of the plant-derived precursor fatty acids (ALA and SDA) and of the potential fatty acid metabolism modulator taurine to increase n3-LC-PUFAS and their respective oxylipins in human plasma and cultivated hepatocytes (HepG2 cells).
In a monocentric, randomized crossover study 29 healthy male volunteers received three sequential interventions, namely ahiflower oil (9 g/day), taurine (1.5 g/day) and ahiflower oil (9 g/day) + taurine (1.5 g/day) for 20 days. In addition, cultivated HepG2 cells were treated with isolated fatty acids ALA, SDA, EPA, DHA as well as taurine alone or together with SDA.
Oral ahiflower oil intake significantly improved plasma EPA levels (0.2 vs. 0.6% of total fatty acid methyl esters (FAMES)) in humans, whereas DHA levels were unaffected by treatments. EPA-levels in SDA-treated HepG2 cells were 65% higher (5.1 vs. 3.0% of total FAMES) than those in ALA-treated cells. Taurine did not affect fatty acid profiles in human plasma or in HepG2 cells . SDA-rich ahiflower oil and isolated SDA led to an increase in EPA-derived oxylipins in humans and in HepG2 cells, respectively.
The consumption of ahiflower oil improves the circulating levels of EPA and EPA-derived oxylipins in humans. In cultivated hepatocytes, EPA and EPA-derived oxylipins are more effectively increased by SDA than ALA.
来自 种子的阿西洛花油富含α-亚麻酸(ALA)和硬脂酸(SDA)。ALA和SDA是人体内二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)内源性合成的潜在前体脂肪酸,这两种酸都是n-3长链多不饱和脂肪酸(n3-LC-PUFAS)。由于牛磺酸(一种氨基磺酸)常与富含n3-LC-PUFAS的组织相关(如在富含脂肪的鱼类、人类视网膜中),牛磺酸可能在EPA和DHA的代谢中发挥作用。
研究植物来源的前体脂肪酸(ALA和SDA)以及潜在的脂肪酸代谢调节剂牛磺酸增加人体血浆和培养的肝细胞(HepG2细胞)中n3-LC-PUFAS及其各自氧化脂质的能力。
在一项单中心随机交叉研究中,29名健康男性志愿者接受了三项连续干预,即阿西洛花油(9克/天)、牛磺酸(1.5克/天)和阿西洛花油(9克/天)+牛磺酸(1.5克/天),为期20天。此外,用分离出的脂肪酸ALA、SDA、EPA、DHA以及单独的牛磺酸或与SDA一起处理培养的HepG2细胞。
口服阿西洛花油显著提高了人体血浆中的EPA水平(从总脂肪酸甲酯(FAMES)的0.2%提高到0.6%),而DHA水平不受治疗影响。用SDA处理的HepG2细胞中的EPA水平比用ALA处理的细胞高65%(分别占总FAMES的5.1%和3.0%)。牛磺酸不影响人体血浆或HepG2细胞中的脂肪酸谱。富含SDA的阿西洛花油和分离出的SDA分别导致人体和HepG2细胞中EPA衍生的氧化脂质增加。
食用阿西洛花油可提高人体中EPA和EPA衍生的氧化脂质的循环水平。在培养的肝细胞中,SDA比ALA更有效地增加EPA和EPA衍生的氧化脂质。