Laboratory of Experimental Surgery, Université Libre de Bruxelles, Brussels, Belgium.
Am J Clin Nutr. 2010 Apr;91(4):875-82. doi: 10.3945/ajcn.2009.27951. Epub 2010 Feb 10.
Dietary deficiency in n-3 (omega-3) polyunsaturated fatty acids (PUFAs) prevails in Western populations and potentially results in adverse health outcomes. To circumvent the slow n-3 PUFA incorporation in phospholipids of key cells after oral supplementation, a new preparation for intravenous bolus injection was developed with 20 g triacylglycerols/100 mL of a mixture of 80% medium-chain triacylglycerols (MCTs) and 20% fish oil (FO) (wt:wt), and 0.4 g alpha-tocopherol/100 mL of the same mixture.
Our objective was to document the enrichment of n-3 PUFAs in leukocyte and platelet phospholipids after a bolus intravenous injection of MCT:FO in men.
Twelve healthy male subjects received injections over a 5-min period of 50 mL of either MCT:FO or a control MCT:long-chain triacylglycerol (MCT:LCT) emulsion containing 20 g triacylglycerols/100 mL with equal amounts (wt:wt) of MCT and soybean triacylglycerols (LCT) and containing 0.02 g alpha-tocopherol/100 mL; after an 8-wk interval, the subjects received injections of the other preparation.
Clinical and biological variables that assessed tolerance and safety remained unchanged. Plasma elimination was faster for MCT:FO than for MCT:LCT (half-life: 24.5 +/- 3.5 min compared with 32.9 +/- 3.0 min; P < 0.025). This was associated with a greater increase in the plasma nonesterified fatty acid concentration. The content of n-3 PUFAs, specifically eicosapentaenoic acid (20:5n-3), increased in leukocyte and platelet phospholipids within 60 min and > or =24 h after MCT:FO injection.
Bolus intravenous injection of a novel MCT:FO emulsion allows rapid enrichment of cells with n-3 PUFAs.
在西方人群中,n-3(ω-3)多不饱和脂肪酸(PUFAs)的饮食缺乏可能导致不良的健康后果。为了避免口服补充后关键细胞内磷脂中 n-3 PUFA 的缓慢掺入,开发了一种新的静脉推注制剂,由 20 g 三酰基甘油/100 mL 80%中链三酰基甘油(MCT)和 20%鱼油(FO)(wt:wt)的混合物以及 0.4 g α-生育酚/100 mL 相同混合物组成。
我们的目的是记录男性静脉推注 MCT:FO 后白细胞和血小板磷脂中 n-3 PUFAs 的富集情况。
12 名健康男性受试者在 5 分钟内接受 50 mL 以下两种制剂之一的注射:MCT:FO 或对照 MCT:长链三酰基甘油(MCT:LCT)乳剂,每 100 mL 含 20 g 三酰基甘油,MCT 和大豆三酰基甘油(LCT)的比例相同(wt:wt),并含有 0.02 g α-生育酚/100 mL;8 周间隔后,受试者接受另一种制剂的注射。
评估耐受性和安全性的临床和生物学变量保持不变。MCT:FO 的血浆消除速度快于 MCT:LCT(半衰期:24.5±3.5 分钟比 32.9±3.0 分钟;P<0.025)。这与血浆非酯化脂肪酸浓度的更大增加有关。n-3 PUFAs,特别是二十碳五烯酸(20:5n-3),在 MCT:FO 注射后 60 分钟内和≥24 小时内增加白细胞和血小板磷脂中的含量。
新型 MCT:FO 乳剂的静脉推注可快速使细胞富含 n-3 PUFAs。