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高脂肪饮食可削弱脂多糖刺激的 Wistar 大鼠腹腔巨噬细胞核因子-κB 信号通路的激活。

High-fat diet blunts activation of the nuclear factor-κB signaling pathway in lipopolysaccharide-stimulated peritoneal macrophages of Wistar rats.

机构信息

Department of Nutrition, School of Public Health, University of Sao Paulo, Sao Paulo, Brazil.

出版信息

Nutrition. 2013 Feb;29(2):443-9. doi: 10.1016/j.nut.2012.06.008. Epub 2012 Oct 22.

Abstract

OBJECTIVE

The present study was designed to investigate the effect of a high-fat diet (HFD) on the inflammatory response of peritoneal macrophages.

METHODS

Male Wistar rats were fed a control diet (n = 12) or an HFD (n = 12) for 12 wk. After euthanasia, peritoneal macrophages were collected and stimulated (or not) with lipopolysaccharide (LPS). Results from the assays using peritoneal macrophages were analyzed with one-way analysis of variance or an equivalent non-parametric test. The level of significance adopted was 0.05.

RESULTS

Consumption of the HFD was associated with significant increases in weight gain and fat depots (P < 0.05). Despite having no influence in systemic markers of inflammation, such as interleukin (IL)-6, tumor necrosis factor-α, and plasminogen activator inhibitor-1, the HFD intake significantly decreased insulin sensitivity, as evaluated by the homeostasis model assessment index (P < 0.05). A decreased production of IL-1β, IL-6, IL-10, and nitric oxide in response to the LPS stimulation was observed in peritoneal macrophages from the HFD group (P < 0.05). Also, in HFD-fed animals, LPS incubation did not increase IL-1β and IL-6 mRNA expression (P < 0.05). These effects were associated with an attenuation of IκB inhibitor kinase-β phosphorylation and nuclear factor-κB activation in response to LPS and with a failure to decrease IκB inhibitor-α expression (P < 0.05).

CONCLUSION

Chronic consumption of an HFD decreased the LPS-induced inflammatory response of peritoneal macrophages, which was associated with a downregulation of the nuclear factor-κB signaling pathway.

摘要

目的

本研究旨在探讨高脂肪饮食(HFD)对腹腔巨噬细胞炎症反应的影响。

方法

雄性 Wistar 大鼠分别给予对照饮食(n = 12)或 HFD(n = 12)喂养 12 周。安乐死后收集腹腔巨噬细胞,并用脂多糖(LPS)刺激(或不刺激)。采用单因素方差分析或等效的非参数检验分析腹腔巨噬细胞的检测结果。采用的显著性水平为 0.05。

结果

摄入 HFD 与体重增加和脂肪沉积显著增加有关(P < 0.05)。尽管 HFD 摄入对全身炎症标志物(如白细胞介素(IL)-6、肿瘤坏死因子-α和纤溶酶原激活物抑制剂-1)没有影响,但通过稳态模型评估指数(HOMA-IR)评估,HFD 摄入显著降低了胰岛素敏感性(P < 0.05)。与 LPS 刺激相关的腹腔巨噬细胞中 IL-1β、IL-6、IL-10 和一氧化氮的产生显著减少(P < 0.05)。此外,在 HFD 喂养的动物中,LPS 孵育并未增加 IL-1β 和 IL-6 mRNA 的表达(P < 0.05)。这些作用与 LPS 诱导的 IκB 抑制剂激酶-β磷酸化和核因子-κB 激活的减弱以及 IκB 抑制剂-α表达的减少有关(P < 0.05)。

结论

慢性摄入 HFD 降低了 LPS 诱导的腹腔巨噬细胞炎症反应,这与核因子-κB 信号通路的下调有关。

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