Alden P B, Svingen B A, Johnson S B, Konstantinides F N, Holman R T, Cerra F B
Surgery. 1986 Oct;100(4):671-8.
Polyunsaturated fatty acid (PUFA) profiles are abnormal in a variety of clinical conditions that are commonly seen in the surgical intensive care unit. PUFA profiles in the serum phospholipids were studied by capillary gas chromatography in 22 critically ill, hypermetabolic surgical intensive care unit patients. All patients received continuous total parenteral nutrition (TPN) by central vein with trace elements and vitamins. Eleven patients received daily supplementation with 50 gm of safflower oil-based lipid emulsion (TPN + L group). No lipid was administered in the other 11 patients (TPN). Both groups showed deficiencies in 18:2 omega 6 linoleic acid from the time of onset of TPN. In TPN the deficiency was progressive; in the TPN + L group, lipid administration prevented this progression but did not restore 18:2 omega 6 levels to normal. In the TPN group levels of 18:1 omega 9 and its metabolite 20:3 omega 9 (the triene of deficiency) increased over time, consistent with a mild essential fatty acid deficiency. These changes in omega 9 acids were not seen with lipid supplementation. Despite low levels of 18:2 omega 6 in both groups, the levels of omega 6 metabolites were normal or increased. Levels of 20:4 omega 6 (arachidonate) remained normal or slightly decreased in the TPN group but were decreased in the TPN + L group. Levels of arachidonate metabolites, in particular 22:5 omega 6, were increased in the lipid-supplemented group. We concluded that stressed patients receiving TPN develop mild essential fatty acid deficiency that is only partially correctable by lipid supplementation and that administration of supplemental lipid to these patients stimulates arachidonic acid conversion to 22:5 omega 6.
多不饱和脂肪酸(PUFA)谱在外科重症监护病房常见的多种临床病症中存在异常。我们通过毛细管气相色谱法研究了22例危重症、高代谢的外科重症监护病房患者血清磷脂中的PUFA谱。所有患者均通过中心静脉接受含微量元素和维生素的持续全胃肠外营养(TPN)。11例患者每日补充50克红花油基脂质乳剂(TPN + L组)。另外11例患者未给予脂质(TPN组)。两组从TPN开始时就显示出18:2 ω6亚油酸缺乏。在TPN组中,这种缺乏呈进行性;在TPN + L组中,给予脂质可阻止这种进展,但未使18:2 ω6水平恢复正常。在TPN组中,18:1 ω9及其代谢产物20:3 ω9(缺乏的三烯)水平随时间升高,这与轻度必需脂肪酸缺乏一致。补充脂质后未出现ω9酸的这些变化。尽管两组中18:2 ω6水平较低,但ω6代谢产物水平正常或升高。20:4 ω6(花生四烯酸)水平在TPN组中保持正常或略有下降,但在TPN + L组中下降。补充脂质组中花生四烯酸代谢产物水平,尤其是22:5 ω6升高。我们得出结论,接受TPN的应激患者会出现轻度必需脂肪酸缺乏,脂质补充只能部分纠正这种缺乏,并且给这些患者补充脂质会刺激花生四烯酸转化为22:5 ω6。