Clark Louise F, Thivierge M C, Kidd Claire A, McGeoch Susan C, Abraham Prakash, Pearson Donald W M, Horgan Graham W, Holtrop Grietje, Thies Frank, Lobley Gerald E
1The Rowett Institute of Nutrition and Health,University of Aberdeen,Aberdeen AB21 9SB,UK.
2Aberdeen Diabetes Centre,Aberdeen Royal Infirmary,Aberdeen AB25 2ZP,UK.
Br J Nutr. 2016 Jan 14;115(1):75-86. doi: 10.1017/S0007114515004274. Epub 2015 Nov 5.
The effects of fish oil (FO) supplementation on glycaemic control are unclear, and positive effects may occur only when the phospholipid content of tissue membranes exceeds 14% as n-3 PUFA. Subjects (n 36, thirty-three completed) were paired based on metabolic parameters and allocated into a parallel double-blind randomised trial with one of each pair offered daily either 6 g of FO (3·9 g n-3 PUFA) or 6 g of maize oil (MO) for 9 months. Hyperinsulinaemic-euglycaemic-euaminoacidaemic (HIEGEAA) clamps (with [6,6 2H2 glucose]) were performed at the start and end of the intervention. Endogenous glucose production (EGP) and whole-body protein turnover (WBPT) were each measured after an overnight fast. The primary outcome involved the effect of oil type on insulin sensitivity related to glycaemic control. The secondary outcome involved the effect of oil type on WBPT. Subjects on FO (n 16) had increased erythrocyte n-3 PUFA concentrations >14%, whereas subjects on MO (n 17) had unaltered n-3 PUFA concentrations at 9%. Type of oil had no effect on fasting EGP, insulin sensitivity or total glucose disposal during the HIEGEAA clamp. In contrast, under insulin-stimulated conditions, total protein disposal (P=0·007) and endogenous WBPT (P=0·001) were both increased with FO. In an associated pilot study (n 4, three completed), although n-3 PUFA in erythrocyte membranes increased to >14% with the FO supplement, the enrichment in muscle membranes remained lower (8%; P<0·001). In conclusion, long-term supplementation with FO, at amounts near the safety limits set by regulatory authorities in Europe and the USA, did not alter glycaemic control but did have an impact on WBPT.
补充鱼油(FO)对血糖控制的影响尚不清楚,且可能只有当组织膜中的磷脂含量超过14%(以n-3多不饱和脂肪酸计)时才会产生积极效果。根据代谢参数将受试者(n = 36,33人完成试验)配对,并分配到一项平行双盲随机试验中,每对中的一人每天服用6 g FO(3.9 g n-3多不饱和脂肪酸),另一人每天服用6 g玉米油(MO),持续9个月。在干预开始和结束时进行高胰岛素-正常血糖-正常氨基酸(HIEGEAA)钳夹试验(使用[6,6-2H2葡萄糖])。过夜禁食后分别测量内源性葡萄糖生成(EGP)和全身蛋白质周转(WBPT)。主要结局涉及油的类型对与血糖控制相关的胰岛素敏感性的影响。次要结局涉及油的类型对WBPT的影响。服用FO的受试者(n = 16)红细胞n-3多不饱和脂肪酸浓度增加至>14%,而服用MO的受试者(n = 17)的n-3多不饱和脂肪酸浓度保持在9%不变。油的类型对HIEGEAA钳夹试验期间的空腹EGP、胰岛素敏感性或总葡萄糖处置没有影响。相反,在胰岛素刺激条件下,服用FO后总蛋白质处置(P = 0.007)和内源性WBPT(P = 0.001)均增加。在一项相关的试点研究(n = 4,3人完成试验)中,尽管补充FO后红细胞膜中的n-3多不饱和脂肪酸增加至>14%,但肌肉膜中的富集仍较低(8%;P<0.001)。总之,长期补充接近欧洲和美国监管机构设定的安全限量的FO,不会改变血糖控制,但会对WBPT产生影响。