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膳食中的n-3多不饱和脂肪酸可预防小鼠动脉粥样硬化病变的发展。巨噬细胞分泌活动的调节。

Dietary n-3 polyunsaturated fatty acids prevent the development of atherosclerotic lesions in mice. Modulation of macrophage secretory activities.

作者信息

Renier G, Skamene E, DeSanctis J, Radzioch D

机构信息

Department of Experimental Medicine, McGill Centre for the Study of Host Resistance, Montreal General Hospital Research Institute, Quebec, Canada.

出版信息

Arterioscler Thromb. 1993 Oct;13(10):1515-24. doi: 10.1161/01.atv.13.10.1515.

Abstract

We examined the effects of dietary n-3 polyunsaturated and saturated fatty acids on the development of the atherogenic process in mice and on the macrophage ability to secrete several effector molecules that may be involved in the atherogenic process. The secretion of inflammatory proteins such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) and the production of lipoprotein lipase (LPL), nitrogen oxide (NO2), and prostaglandin E2 (PGE2) were evaluated in peritoneal macrophages isolated from atherosclerosis-susceptible C57BL/6J mice. The mice were assigned at random to three experimental groups: the first group was fed a semi-defined control diet (control diet); the second group was maintained on the control diet supplemented with 10% menhaden oil (menhaden diet); and the third group received the control diet supplemented with 10% palm oil plus 2% cholesterol (saturated fat diet). Macrophages derived from mice fed the menhaden diet showed a suppression of their basal TNF-alpha mRNA expression and production. They also presented a dramatically decreased ability to express TNF-alpha and IL-1 beta mRNAs in response to exposure to lipopolysaccharide (LPS) compared with the macrophages from the control group. LPL mRNA and protein expression were downregulated after 6 and 15 weeks of menhaden-diet feeding. Significantly higher NO2 production in response to interferon gamma was found, both after 6 and 15 weeks of diet feeding, in the menhaden group compared with the control group. In addition, prostaglandin production and macrophage tumoricidal activity in response to LPS were decreased in this group compared with the control group. Macrophages derived from the saturated fat group did not show any significant alterations in TNF-alpha, LPL, NO2, or PGE2 secretion compared with controls. Interestingly, we observed a progressive increase of the LPS-induced IL-1 beta gene expression and secretion among macrophages harvested from mice receiving the dietary supplement of saturated fatty acids. At 6 and 15 weeks histologic examination of the atherosclerotic lesions did not reveal any important lesions in the control and menhaden groups, whereas a gradual development of fatty streaks was observed in the menhaden experimental diets for 10 additional weeks resulted in a major development of lesions in the control group, whereas only slight lesions were observed in the menhaden group.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们研究了膳食中的n-3多不饱和脂肪酸和饱和脂肪酸对小鼠动脉粥样硬化形成过程的影响,以及对巨噬细胞分泌几种可能参与动脉粥样硬化形成过程的效应分子能力的影响。在从易患动脉粥样硬化的C57BL/6J小鼠分离出的腹腔巨噬细胞中,评估了炎症蛋白如肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)的分泌,以及脂蛋白脂肪酶(LPL)、一氧化氮(NO₂)和前列腺素E₂(PGE₂)的产生。将小鼠随机分为三个实验组:第一组喂食半限定对照饮食(对照饮食);第二组维持在添加10%鲱鱼油的对照饮食上(鲱鱼饮食);第三组接受添加10%棕榈油加2%胆固醇的对照饮食(饱和脂肪饮食)。喂食鲱鱼饮食的小鼠来源的巨噬细胞显示其基础TNF-α mRNA表达和产生受到抑制。与对照组的巨噬细胞相比,它们在暴露于脂多糖(LPS)时表达TNF-α和IL-1β mRNA的能力也显著降低。喂食鲱鱼饮食6周和15周后,LPL mRNA和蛋白表达下调。与对照组相比,在饮食喂养6周和15周后,鲱鱼组中对干扰素γ反应产生的NO₂显著更高。此外,与对照组相比,该组中对LPS反应的前列腺素产生和巨噬细胞杀肿瘤活性降低。与对照组相比,饱和脂肪组来源的巨噬细胞在TNF-α、LPL、NO₂或PGE₂分泌方面未显示任何显著变化。有趣的是,我们观察到在接受饱和脂肪酸膳食补充的小鼠收获的巨噬细胞中,LPS诱导的IL-1β基因表达和分泌逐渐增加。在6周和15周时,对动脉粥样硬化病变的组织学检查在对照组和鲱鱼组中未发现任何重要病变,而在鲱鱼组中观察到脂肪条纹逐渐发展。在另外10周的鲱鱼实验饮食后,对照组中病变大量发展,而鲱鱼组中仅观察到轻微病变。(摘要截短至400字)

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