Parenteral supplementation with a fish-oil emulsion prolongs survival and improves rat lymphocyte function during sepsis

Citation
S. Lanza-jacoby et al., Parenteral supplementation with a fish-oil emulsion prolongs survival and improves rat lymphocyte function during sepsis, NUTRITION, 17(2), 2001, pp. 112-116
Citations number
33
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
NUTRITION
ISSN journal
08999007 → ACNP
Volume
17
Issue
2
Year of publication
2001
Pages
112 - 116
Database
ISI
SICI code
0899-9007(200102)17:2<112:PSWAFE>2.0.ZU;2-A
Abstract
Nutritional intervention with omega -3 fatty acids during trauma and infect ion has been shown to improve the clinical outcome of patients and the surv ival rate in laboratory animals. This study evaluated the effects of parent eral administration of lipid emulsions containing fish oil (FO) or soybean oil (SBO) on survival and T-lymphocyte response during sepsis. Male Sprague -Dawley rats (250-275 g) were prepared for parenteral feeding 4 d before in ducing sepsis by cecal ligation and puncture (CLP). Standard resuscitation was provided with normal saline. Thirty minutes after completing CLP, sham control or CLP rats were infused continuously with saline or a parenteral d iet containing SBO or a 1:1 FO:SBO emulsion. The survival rate was signific antly improved in rats receiving the FO-supplemented diet, with 50% alive b y 120 h in comparison with the saline-infused, chow-fed rats (0% alive by 1 20 h) or the SBO-fed rats (12% alive at 120 h. The T-lymphocyte response wa s evaluated at 24 h after CLP. Sepsis led to a decline in lymphocyte prolif eration in rats infused with saline or the SBO emulsion, which was associat ed with a greater release of splenocyte interleukin-10, transforming growth factor-beta and prostaglandin E-2. Administering the 1:1 FO:SBO parenteral diet during sepsis improved the survival rate and prevented the sepsis-ind uced suppression of lymphocyte proliferation and interleukin-2 release. The FO effect on lymphocyte function was associated with decreased splenocyte release of transforming growth factor-beta and prostaglandin E-2. (C) Elsev ier Science Inc. 2001.