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给肥胖的瘦素受体缺陷型JCR:LA-cp大鼠喂食长链n-3多不饱和脂肪酸可改变免疫功能和脂筏脂肪酸组成。

Feeding long-chain n-3 polyunsaturated fatty acids to obese leptin receptor-deficient JCR:LA- cp rats modifies immune function and lipid-raft fatty acid composition.

作者信息

Ruth Megan R, Proctor Spencer D, Field Catherine J

机构信息

Nutrition & Metabolism Research Group, University of Alberta, Edmonton, AB T6G 2P5, Canada.

出版信息

Br J Nutr. 2009 May;101(9):1341-50. doi: 10.1017/S0007114508076277. Epub 2008 Dec 15.

Abstract

Dietary EPA and DHA modulate immunity and thereby may improve the aberrant immune function in obese states. To determine the effects of feeding fish oil (FO) containing EPA and DHA on splenocyte phospholipid (PL) and lipid-raft fatty acid composition, phenotypes and cytokine production, 14-week-old obese, leptin receptor-deficient JCR:LA-cp rats (cp/cp; n 10) were randomised to one of three nutritionally adequate diets for 3 weeks: control (Ctl, 0 % EPA+DHA); low FO (LFO, 0.8 % (w/w) EPA+DHA); high FO (HFO, 1.4 % (w/w) EPA+DHA). Lean JCR:LA-cp (+/ - or +/+) rats (n 5) were fed the Ctl diet. Obese Ctl rats had a higher proportion of n-3 PUFA in splenocyte PL than lean rats fed the same diet (P < 0.05). The lower n-6:n-3 PUFA ratio of splenocyte PL was consistent with the lower mitogen-stimulated interferon (IFN)-gamma and IL-1beta production by cells from obese rats (P < 0.05). Obese rats fed the FO diet had lower mitogen-stimulated Th1 (IFN-gamma) and Th2 (IL-4) cytokine responses, but IL-2 production (concanavalin A; ConA) did not differ (P < 0.05). The HFO diet was more effective in lowering IL-1beta and increasing IL-10 production (ConA, P < 0.05). This lower IL-1beta production was accompanied by a lower proportion of major histocompatability complex class II-positive cells and a higher incorporation of DHA into lipid rafts. This is the first study to demonstrate impaired responses to mitogen stimulation and altered fatty acid incorporation into the membrane PL of JCR:LA-cp rats. Feeding FO lowered the ex vivo inflammatory response, without altering IL-2 production from ConA-stimulated splenocytes which may occur independent of leptin signalling.

摘要

膳食中的二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)可调节免疫,从而可能改善肥胖状态下异常的免疫功能。为了确定喂食含EPA和DHA的鱼油(FO)对脾细胞磷脂(PL)、脂筏脂肪酸组成、表型及细胞因子产生的影响,将14周龄肥胖、瘦素受体缺陷的JCR:LA-cp大鼠(cp/cp;n = 10)随机分为三种营养充足的饮食组之一,持续3周:对照组(Ctl,0% EPA + DHA);低鱼油组(LFO,0.8%(w/w)EPA + DHA);高鱼油组(HFO,1.4%(w/w)EPA + DHA)。将瘦的JCR:LA-cp(+/ - 或 +/+)大鼠(n = 5)喂食Ctl饮食。肥胖的Ctl大鼠脾细胞PL中n-3多不饱和脂肪酸(PUFA)的比例高于喂食相同饮食的瘦大鼠(P < 0.05)。脾细胞PL中较低的n-6:n-3 PUFA比值与肥胖大鼠细胞经丝裂原刺激产生的干扰素(IFN)-γ和白细胞介素(IL)-1β较低一致(P < 0.05)。喂食FO饮食的肥胖大鼠经丝裂原刺激的Th1(IFN-γ)和Th2(IL-4)细胞因子反应较低,但IL-2产生(刀豆蛋白A;ConA)无差异(P < 0.05)。HFO饮食在降低IL-1β和增加IL-10产生方面更有效(ConA,P < 0.05)。这种较低的IL-1β产生伴随着主要组织相容性复合体II类阳性细胞比例降低以及DHA掺入脂筏增加。这是第一项证明JCR:LA-cp大鼠对丝裂原刺激反应受损以及脂肪酸掺入膜PL改变的研究。喂食FO可降低体外炎症反应,而不改变ConA刺激的脾细胞产生IL-2,这可能独立于瘦素信号发生。

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