Western diet enhances hepatic inflammation in mice exposed to cecal ligation and puncture.

Q1 Biochemistry, Genetics and Molecular Biology
Chantal A Rivera, LaTausha Gaskin, Georg Singer, Jeff Houghton, Monique Allman
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引用次数: 31

Abstract

Background: Obese patients display an exaggerated morbidity during sepsis. Since consumption of a western-style diet (WD) is a major factor for obesity in the United States, the purpose of the present study was to examine the influence of chronic WD consumption on hepatic inflammation in mice made septic via cecal ligation and puncture (CLP). Feeding mice diets high in fat has been shown to enhance evidence of TLR signaling and this pathway also mediates the hepatic response to invading bacteria. Therefore, we hypothesized that the combined effects of sepsis and feeding WD on TRL-4 signaling would exacerbate hepatic inflammation. Male C57BL/6 mice were fed purified control diet (CD) or WD that was enriched in butter fat (34.4% of calories) for 3 weeks prior to CLP. Intravital microscopy was used to evaluate leukocyte adhesion in the hepatic microcirculation. To demonstrate the direct effect of saturated fatty acid on hepatocytes, C3A human hepatocytes were cultured in medium containing 100 μM palmitic acid (PA). Quantitative real-time PCR was used to assess mRNA expression of tumor necrosis factor-alpha (TNF-α, monocyte chemotactic protein-1 (MCP-1), intercellular adhesion molecule-1 (ICAM-1), toll-like receptor-4 (TLR-4) and interleukin-8 (IL-8).

Results: Feeding WD increased firm adhesion of leukocytes in the sinusoids and terminal hepatic venules by 8-fold six hours after CLP; the increase in platelet adhesion was similar to the response observed with leukocytes. Adhesion was accompanied by enhanced expression of TNF-α, MCP-1 and ICAM-1. Messenger RNA expression of TLR-4 was also exacerbated in the WD+CLP group. Exposure of C3A cells to PA up-regulated IL-8 and TLR-4 expression. In addition, PA stimulated the static adhesion of U937 monocytes to C3A cells, a phenomenon blocked by inclusion of an anti-TLR-4/MD2 antibody in the culture medium.

Conclusions: These findings indicate a link between obesity-enhanced susceptibility to sepsis and consumption of a western-style diet.

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西方饮食增加盲肠结扎和穿刺小鼠肝脏炎症。
背景:肥胖患者在败血症期间的发病率较高。由于西式饮食(WD)是美国肥胖的主要因素,本研究的目的是研究慢性WD消费对盲肠结扎穿刺(CLP)脓毒症小鼠肝脏炎症的影响。给小鼠喂食高脂肪食物已被证明可以增强TLR信号通路,该通路也介导肝脏对入侵细菌的反应。因此,我们假设脓毒症和饲喂WD对TRL-4信号的联合作用会加重肝脏炎症。雄性C57BL/6小鼠在CLP前3周饲喂纯化对照饲料(CD)或富含黄油脂肪(34.4%的热量)的WD。活体显微镜观察肝微循环白细胞粘附情况。为了证明饱和脂肪酸对肝细胞的直接作用,我们在含有100 μM棕榈酸(PA)的培养基中培养C3A人肝细胞。采用实时荧光定量PCR检测肿瘤坏死因子-α (TNF-α)、单核细胞趋化蛋白-1 (MCP-1)、细胞间粘附分子-1 (ICAM-1)、toll样受体-4 (TLR-4)和白细胞介素-8 (IL-8) mRNA的表达。结果:给药WD使CLP后6小时肝窦和终末小静脉内白细胞的牢固粘附增加了8倍;血小板粘附的增加与白细胞的反应相似。粘附过程中,TNF-α、MCP-1、ICAM-1表达增强。WD+CLP组TLR-4信使RNA表达也增加。暴露于PA的C3A细胞上调了IL-8和TLR-4的表达。此外,PA刺激U937单核细胞与C3A细胞的静态粘附,这一现象通过在培养基中加入抗tlr -4/MD2抗体而被阻断。结论:这些发现表明肥胖增加的败血症易感性与西式饮食的消费之间存在联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Physiology
BMC Physiology Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
9.60
自引率
0.00%
发文量
0
期刊介绍: BMC Physiology is an open access journal publishing original peer-reviewed research articles in cellular, tissue-level, organismal, functional, and developmental aspects of physiological processes. BMC Physiology (ISSN 1472-6793) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record and Google Scholar.
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