Increased survival after cecal ligation and puncture in mice consuming diets enriched with sesame seed oil

Citation
Sr. Chavali et al., Increased survival after cecal ligation and puncture in mice consuming diets enriched with sesame seed oil, CRIT CARE M, 29(1), 2001, pp. 140-143
Citations number
35
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
29
Issue
1
Year of publication
2001
Pages
140 - 143
Database
ISI
SICI code
0090-3493(200101)29:1<140:ISACLA>2.0.ZU;2-#
Abstract
Objectives: Lignans that present in the nonfat portion of sesame seed oil ( SSO) can inhibit Delta -5 desaturase activity, resulting in an increase in the accumulation of dihomo-gamma -linolenic acid and, subsequently, decreas e the production of proinflammatory dienoic eicosanoids with a concomitant increase in the secretion of less inflammatory monoenoic eicosanoids. Design: Female Balb/c mice were fed diets supplemented with 5wt% SSO or a p hysical mixture of oils (control) whose fatty acid composition resembled th at of SSO for 3 wks. Measurements and Main Results: During a 4-day observation period after ceca l ligation and puncture, only 20% of the controls and as many as 65% in the SSO group survived. Furthermore, the levels of cytokines and dienoic eicos anoids produced in response to an intraperitoneal injection of a nonlethal dose (50 mug/mouse) of endotoxin were measured in both groups. The interleu kin (IL)-10 levels were markedly higher in mice fed SSO diets compared with the controls. However, the plasma concentrations of prostaglandin E-1 (+) (2), tumor necrosis factor-alpha, IL-6, and IL-12 did not differ significan tly between the two groups of mice. Conclusions: Because the fatty acid composition is almost similar between t he two diets, sesamin, sesamol and other lignans in SSO appear to be respon sible for an increase in survival after cecal ligation and puncture and als o for an increase in the IL-10 levels in response to a nonlethal dose of en dotoxin in mice.