Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

CiteULike is a free service for managing and discovering scholarly references - click here to get started.

Sign In to gain access to subscriptions and/or personal tools.
Journal of Parenteral and Enteral Nutrition
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Sax, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sax, H.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Medline Plus Health Information
*Dietary Fats
*E. Coli Infections
*Staphylococcal Infections
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Composition of Fat in Enteral Diets Can Influence Outcome in Experimental Peritonitis M. D. PECK, C. K. OGLE, J. W. ALEXANDER Annals of Surgery 214:74-82, 1991

Harry Sax, MD

University of Rochester Rochester, NY

The potential immunosuppressive effects of lipids high in the n-6 polyunsaturated fatty acids (PUFA) have led many clinicians to recommend limiting fat intake in stressed patients. Similarly, experimental and clinical evidence has been presented that supports the use of lipid formulations enriched in the marine-based n-3 PUFA in these patients.1,2

This paper describes an experimental study designed to address the effect of dietary fat composition on outcome in an animal model of chronic intra-abdominal sepsis. Guinea pigs underwent gastrostomies and were later implanted with osmotic pumps inoculated with a mixture of Escherichia coli and Staphylococcus aureus. A steady infusion of this synergistic combination of bacteria into the peritoneal cavity resulted in an animal model of chronic intra-abdominal sepsis. Animals were randomized to one of three dietary groups according to the level of fat intake: 3.5%, 14%, and 56% of total calories. Within each of these groups, fat composition was either high in n-6 PUFA (100% Microlipid), high in n-3 PUFA (100% maximum eicosapentaenoic acid [MaxEPA]) or a 50:50 mixture of the two.

Animal survival was not significantly altered by the amount of fat in the diet (Kruskal-Wallis analysis of variance, p > .1). However, the dietary fat composition had a significant overall effect (p < .05) on the length of survival. Median survival in the 50:50 group was 12.5 days, significantly longer than that in the 100% MaxEPA group (9 days), p = .011), but not significantly longer than that in the 100% Microlipid group (10 days, p = .082).

In another experiment animals were fed a 14% total fat calorie diet. A total of five subgroups were created, with fat ratios (Microlipid/MaxEPA) of 100/0, 25/75, 50/50, 75/25, and 0/100. Survival was greatest in the group of animals given equal amounts of fat types: 18%, 25%, 84%, 42%, and 36% (p = .023, 50:50 group vs all other groups).

No major differences in immunologic parameters among the various groups were noted, except for an increase in lipopolysaccharide-stimulated prostaglandin E2 production by splenic macrophages in the 100% Microlipid group (p = .03).

Journal of Parenteral and Enteral Nutrition, Vol. 16, No. 1, 87 (1992)
DOI: 10.1177/014860719201600187


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?