Innis S M, Yuen D E
Department of Paediatrics, University of British Columbia, Vancouver, Canada.
Lipids. 1988 Jun;23(6):546-50. doi: 10.1007/BF02535595.
The effect of total parenteral nutrition (TPN) with lipid emulsion to supply either 27.5% or 2% total calories on in vitro desaturation-elongation of 18:2(n-6) by liver microsomes was studied in the rat. The emulsion lipid contained ca. 50% 18:2(n-6) plus 8% 18:3(n-3) or 77% 18:2(n-6) plus 0.5% 18:3(n-3). The reaction rate was influenced by the in vitro substrate concentration and inhibited above 50 mumol 18:2(n-6)/mg microsomal protein. At maximum rates of desaturation-elongation, the formation of triene and tetraene (n-6) fatty acids was reduced in rats given either of the two emulsions. The rate of (n-6) pentaene formation was increased in rats given the emulsion with low 18:3(n-3) but not in rats given the emulsion with 8% 18:3(n-3). Analyses of the microsomal lipid indicated increased free cholesterol in all rats that received TPN. Esterified cholesterol was increased only in rats given 27.5% TPN calories as lipid. Microsomal total phospholipids and phospholipid class distributions were not altered by TPN. The data are consistent with reports of reduced levels of long-chain desaturation-elongation metabolites of 18:2(n-6) in tissue phospholipids following infusion of parenteral lipid. The data suggest that the mechanism may include alterations in other metabolic pathways such as cholesterol, in addition to desaturase enzyme activities, and may be influenced by both the quantity and fatty acid composition of the lipid infused.
在大鼠中研究了用提供27.5%或2%总热量的含脂质乳剂的全胃肠外营养(TPN)对肝微粒体将18:2(n-6)进行体外去饱和-延长反应的影响。乳剂脂质约含50%的18:2(n-6)加8%的18:3(n-3)或77%的18:2(n-6)加0.5%的18:3(n-3)。反应速率受体外底物浓度影响,当高于50 μmol 18:2(n-6)/mg微粒体蛋白时受到抑制。在去饱和-延长反应的最大速率时,给予两种乳剂之一的大鼠中三烯和四烯(n-6)脂肪酸的形成减少。给予低18:3(n-3)乳剂的大鼠中(n-6)五烯的形成速率增加,而给予含8% 18:3(n-3)乳剂的大鼠中未增加。微粒体脂质分析表明,所有接受TPN的大鼠中游离胆固醇增加。仅在给予27.5% TPN热量作为脂质的大鼠中酯化胆固醇增加。TPN未改变微粒体总磷脂及其磷脂类分布。这些数据与输注肠外脂质后组织磷脂中18:2(n-6)的长链去饱和-延长代谢产物水平降低的报道一致。数据表明,其机制可能包括除去饱和酶活性外其他代谢途径如胆固醇的改变,并且可能受输注脂质的量和脂肪酸组成两者的影响。