Turner Justine M, Josephson Jessica, Field Catherine J, Wizzard Pamela R, Ball Ronald O, Pencharz Paul B, Wales Paul W
Department of Pediatrics, University of Alberta, Edmonton, Canada Department of Agricultural Food and Nutritional Science, University of Alberta, Edmonton, Canada
Department of Pediatrics, University of Alberta, Edmonton, Canada.
JPEN J Parenter Enteral Nutr. 2016 Sep;40(7):973-81. doi: 10.1177/0148607115579711. Epub 2015 Apr 2.
The optimal parenteral lipid emulsion for neonates should reduce the risk of intestinal failure-associated liver disease and inflammation, while supporting growth and development. This could be best achieved by balanced content of ω-6 and ω-3 polyunsaturated fatty acids (PUFAs). Using a neonatal piglet model of parenteral nutrition (PN), we compared a 100% soy oil-based emulsion (ω-6:ω-3 PUFA: 7:1) with a mixed lipid emulsion comprising 30% soy oil, 30% medium-chain triglycerides, 25% olive oil, and 15% fish oil (ω-6:ω-3 PUFA: approximately 2.5:1) with regard to liver disease, inflammation, and fatty acid content in plasma and brain.
Neonatal piglets, 3-6 days old, underwent jugular catheter insertion for isonitrogenous, isocaloric PN delivery over 14 days. The IL group (n = 8) was treated with Intralipid; the ML group (n = 10) was treated with the mixed lipid (SMOFlipid). Bile flow, liver chemistry, C-reactive protein (CRP), and PUFA content in plasma phospholipids and brain were compared.
Compared with the IL group, ML-treated piglets had increased bile flow (P = .008) and lower total bilirubin (P = .001) and CRP (P = .023) concentrations. The ω-6 long-chain PUFA content was lower in plasma and brain for the ML group. The key ω-3 long-chain PUFA for neonatal development, docosahexaenoic acid (DHA), was not different between groups.
The mixed lipid, having less ω-6 PUFA and more ω-3 PUFA, was able to prevent liver disease and reduce systemic inflammation in PN-fed neonatal piglets. However, this lipid did not increase plasma or brain DHA status, which would be desirable for neonatal developmental outcomes.
适用于新生儿的最佳肠外营养脂质乳剂应降低肠道衰竭相关性肝病和炎症的风险,同时支持生长发育。这可以通过平衡ω-6和ω-3多不饱和脂肪酸(PUFA)的含量来最好地实现。我们使用新生儿仔猪肠外营养(PN)模型,比较了100%大豆油基乳剂(ω-6:ω-3 PUFA为7:1)与包含30%大豆油、30%中链甘油三酯、25%橄榄油和15%鱼油的混合脂质乳剂(ω-6:ω-3 PUFA约为2.5:1)在肝病、炎症以及血浆和脑脂肪酸含量方面的差异。
3至6日龄的新生仔猪接受颈静脉置管,进行为期14天的等氮、等热量PN输注。IL组(n = 8)接受英脱利匹特治疗;ML组(n = 10)接受混合脂质(SMOFlipid)治疗。比较胆汁流量、肝功能、C反应蛋白(CRP)以及血浆磷脂和脑中的PUFA含量。
与IL组相比,接受ML治疗的仔猪胆汁流量增加(P = 0.008),总胆红素(P = 0.001)和CRP(P = 0.023)浓度降低。ML组血浆和脑中的ω-6长链PUFA含量较低。两组间对于新生儿发育关键的ω-3长链多不饱和脂肪酸二十二碳六烯酸(DHA)没有差异。
ω-6 PUFA含量较低且ω-3 PUFA含量较高的混合脂质能够预防PN喂养的新生仔猪发生肝病并减轻全身炎症。然而,这种脂质并未提高血浆或脑中的DHA水平,而这对于新生儿发育结果是有益的。