Decreased production of interleukin-6 and prostaglandin E2 associated with inhibition of Δ-5 desaturation of ω6 fatty acids in mice fed safflower oil diets supplemented with sesamol

被引:24
作者
Chavali, SR [1 ]
Forse, RA [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Surg,Harvard Inst Med, Boston, MA 02118 USA
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 1999年 / 61卷 / 06期
关键词
D O I
10.1054/plef.1999.0112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The differences in the immune responses in mice fed sesame oil diets and those fed sesamin may be attributed to the presence of other lignans in the non-fat portion of the oil. The fatty acid composition (mean +/- SD mel. %) of liver membrane phospholipids and the levels of endotoxin-induced prostaglandin (PG) E-2, interleukin (IL)-6, IL-10, IL-12 and tumor necrosis factor (TNF)-alpha were determined in mice fed diets supplemented with 5% safflower oil (SO) in the absence or presence of 1% sesamol. The levels of dihomo-gamma-linolenic acid (20:3w6) were markedly higher (P < 0.025) in the livers from mice fed sesamol supplemented SO diets (1.6 +/- 0.1) compared to the controls (1.4 +/- 0.1). These data suggest that sesamol or its metabolite could inhibit the in vivo Delta-5 desaturation of w6 fatty acids. Further, in animals fed sesamol supplemented SO diets, the levels of PGE, (228 +/- 41 pg/ml) were markedly lower (P < 0.01) compared to those fed SO diet alone (1355 +/- 188 pg/ml). Concomitantly, the concentrations of IL-6 were also lower (P < 0.01) in mice fed sesamol diet (63 +/- 11 ng/ml) compared to the controls (143 +/- 22 ng/ml). A marked reduction in the levels of PGE, in animals fed sesamol diets suggests that sesamol or its metabolite could inhibit the activity of cycloxygenase enzyme. (C) 1999 Harcourt Publishers Ltd.
引用
收藏
页码:347 / 352
页数:6
相关论文
共 31 条
[1]   Selective inhibition of cyclooxygenase (COX)-2 reverses inflammation and expression of COX-2 and interleukin 6 in rat adjuvant arthritis [J].
Anderson, GD ;
Hauser, SD ;
McGarity, KL ;
Bremer, ME ;
Isakson, PC ;
Gregory, SA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (11) :2672-2679
[2]  
BELLA SD, 1997, PROST LEUK ESSENT FA, V56, P177
[3]   DIETARY SOURCE OF OMEGA-3-FATTY-ACIDS AFFECTS ENDOTOXIN-INDUCED PERITONEAL MACROPHAGE TUMOR-NECROSIS-FACTOR AND EICOSANOID SYNTHESIS [J].
CARRICK, JB ;
SCHNELLMANN, RG ;
MOORE, JN .
SHOCK, 1994, 2 (06) :421-426
[4]   Decreased production of interleukin-1-beta, prostaglandin-E-2, and thromboxane-B-2, and elevated levels of interleukin-6 and -10 are associated with increased survival during endotoxic shock in mice consuming diets enriched with sesame seed oil supplemented with Quil-A saponin [J].
Chavali, SR ;
Zhong, WW ;
Utsunomiya, T ;
Forse, RA .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1997, 114 (02) :153-160
[5]   Increased production of TNF-α and decreased levels of dienoic eicosanoids, IL-6 and IL-10 in mice fed menhaden oil and juniper oil diets in response to an intraperitoneal lethal dose of LPS [J].
Chavali, SR ;
Weeks, CE ;
Zhong, WW ;
Forse, RA .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1998, 59 (02) :89-93
[6]   Dietary α-linolenic acid increases TNF-α, and decreases IL-6, IL-10 in response to LPS:: effects of sesamin on the Δ-5 desaturation of ω6 and ω3 fatty acids in mice [J].
Chavali, SR ;
Zhong, WW ;
Forse, RA .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1998, 58 (03) :185-191
[7]   CYTOKINE SERUM LEVEL DURING SEVERE SEPSIS IN HUMAN IL-6 AS A MARKER OF SEVERITY [J].
DAMAS, P ;
LEDOUX, D ;
NYS, M ;
VRINDTS, Y ;
DEGROOTE, D ;
FRANCHIMONT, P ;
LAMY, M .
ANNALS OF SURGERY, 1992, 215 (04) :356-362
[8]   DIETARY GAMMA-LINOLENIC ACID LOWERS BLOOD-PRESSURE AND ALTERS AORTIC REACTIVITY AND CHOLESTEROL-METABOLISM IN HYPERTENSION [J].
ENGLER, MM .
JOURNAL OF HYPERTENSION, 1992, 10 (10) :1197-1204
[9]   DECREASED INTERLEUKIN-1-BETA LEVELS IN PLASMA FROM RHEUMATOID-ARTHRITIS PATIENTS AFTER DIETARY SUPPLEMENTATION WITH N-3 POLYUNSATURATED FATTY-ACIDS [J].
ESPERSEN, GT ;
NGRUNNET, N ;
LERVANG, HH ;
NIELSEN, GL ;
THOMSEN, BS ;
FAARVANG, KL ;
DYERBERG, J ;
ERNST, E .
CLINICAL RHEUMATOLOGY, 1992, 11 (03) :393-395
[10]  
FOLCH J, 1957, J BIOL CHEM, V226, P497