脂氧素A4对脓毒症肥胖大鼠肝脏TLR4、TRAF6表达的影响

蒋苇苇, 高莉莉, 吴铭, 赵彤, 沈栋林

中国当代儿科杂志 ›› 2018, Vol. 20 ›› Issue (7) : 578-584.

PDF(1400 KB)
HTML
PDF(1400 KB)
HTML
中国当代儿科杂志 ›› 2018, Vol. 20 ›› Issue (7) : 578-584. DOI: 10.7499/j.issn.1008-8830.2018.07.013
论著·实验研究

脂氧素A4对脓毒症肥胖大鼠肝脏TLR4、TRAF6表达的影响

  • 蒋苇苇1, 高莉莉2, 吴铭2, 赵彤2, 沈栋林2
作者信息 +

Effect of lipoxin A4 on the expression of Toll-like receptor 4 and TNF receptorassociated factor 6 in the liver of obese rats with sepsis

  • JIANG Wei-Wei1, GAO Li-Li2, WU Ming2, ZHAO Tong2, SHEN Dong-Ling2
Author information +
文章历史 +

摘要

目的 探讨脂氧素A4(LXA4)对脂多糖诱导肥胖大鼠感染脓毒症的保护作用及其对肝脏Toll样受体4(TLR4)、肿瘤坏死因子受体相关因子6(TRAF6)表达的影响。方法 选取3周龄雄性SpragueDawley大鼠60只随机分为普通组和肥胖组(n=30),建立高脂饮食诱导的肥胖大鼠模型,将两组大鼠再随机分成对照组、脓毒症组、脂氧素组,每组各取8只大鼠。对照组、脓毒症组、脂氧素组分别予生理盐水、脂多糖、脂氧素A4+脂多糖腹腔注射,观察12 h后心脏采血并采集肝脏组织。ELISA法检测血清白细胞介素6(IL-6)及肿瘤坏死因子-α(TNF-α)水平;蛋白免疫印迹法检测肝脏组织TLR4、TRAF6蛋白水平;实时荧光定量PCR法检测TLR4 mRNA、TRAF6 mRNA的表达水平。结果 高脂饮食喂养6周后,肥胖组大鼠的平均体重、Lee's指数明显高于普通组(P < 0.05)。与普通组比较,肥胖组血清IL-6、TNF-α水平明显增高(P < 0.05);同一饮食组内,脓毒症组较对照组血清IL-6、TNF-α水平明显增高(P < 0.05),脂氧素组较脓毒症组血清IL-6、TNF-α水平显著降低(P < 0.05)。与普通组比较,肥胖组大鼠肝脏组织中TLR4、TRAF6蛋白及TLR4 mRNA、TRAF6mRNA表达水平上调(P < 0.05);同一饮食组内,脓毒症组较对照组TLR4、TRAF6蛋白及TLR4 mRNA、TRAF6 mRNA表达量明显增高(P < 0.05),而与脓毒症组比较,脂氧素组TLR4、TRAF6蛋白及TLR4 mRNA、TRAF6 mRNA表达量显著降低(P < 0.05)。结论 LXA4能降低血清IL-6、TNF-α水平,减轻炎症反应。LXA4能抑制TLR4、TRAF6在脓毒症大鼠肝脏中的表达,可能是通过抑制TLR4的信号传导途径来实现的。

Abstract

Objective To study the protective effect of lipoxin A4 (LXA4) against sepsis induced by lipopolysaccharide (LPS) in rats with obesity and its effect on the expression of Toll-like receptor 4 (TLR4) and TNF receptor-associated factor 6 (TRAF6) in the liver.Methods A total of 60 male Sprague-Dawley rats aged three weeks were randomly divided into a normal group and an obesity group, with 30 rats in each group. A rat model of obesity was established by high-fat diet. Each of the two groups was further randomly divided into control group, sepsis group, and LXA4 group, and 8 rats were selected from each group. The rats in the control, sepsis, and LXA4 groups were treated with intraperitoneal injection of normal saline, LPS, and LXA4+LPS respectively. Twelve hours later, blood samples were collected from the heart and liver tissue samples were also collected. ELISA was used to measure the serum levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α). Western blot was used to measure the protein expression of TLR4 and TRAF6 in liver tissue. Quantitative real-time PCR was used to measure the mRNA expression of TLR4 and TRAF6.Results After being fed with high-fat diet for 6 weeks, the obesity group had signifcantly higher average weight and Lee's index than the normal group (P < 0.05). Compared with the normal group, the obesity group had signifcant increases in the serum levels of IL-6 and TNF-α (P < 0.05). In the normal group or the obesity group, the sepsis subgroup had signifcant increases in the serum levels of IL-6 and TNF-α compared with the control subgroup (P < 0.05), while the LXA4 subgroup had signifcant reductions in the two indices compared with the sepsis subgroup (P < 0.05). Compared with the normal group, the obesity group had signifcant increases in the protein and mRNA expression of TLR4 and TRAF6 (P < 0.05). In the normal group or the obesity group, the sepsis subgroup had signifcant increases in the protein and mRNA expression of TLR4 and TRAF6 compared with the control subgroup (P < 0.05). Compared with the sepsis subgroup, the LXA4 subgroup had signifcant reductions in the protein and mRNA expression of TLR4 and TRAF6 (P < 0.05).Conclusions LXA4 can reduce the serum levels of IL-6 and TNF-α and alleviate inflammatory response. LXA4 can inhibit the expression of TLR4 and TRAF6 in the liver of septic rats, possibly by inhibiting the TLR4 signaling pathway.

关键词

肥胖 / 脂多糖 / 脂氧素A4 / Toll样受体4 / 肿瘤坏死因子受体相关因子6 / 大鼠

Key words

Obesity / Lipopolysaccharide / Lipoxin A4 / Toll-like receptor 4 / TNF receptor-associated factor 6 / Rats

引用本文

导出引用
蒋苇苇, 高莉莉, 吴铭, 赵彤, 沈栋林. 脂氧素A4对脓毒症肥胖大鼠肝脏TLR4、TRAF6表达的影响[J]. 中国当代儿科杂志. 2018, 20(7): 578-584 https://doi.org/10.7499/j.issn.1008-8830.2018.07.013
JIANG Wei-Wei, GAO Li-Li, WU Ming, ZHAO Tong, SHEN Dong-Ling. Effect of lipoxin A4 on the expression of Toll-like receptor 4 and TNF receptorassociated factor 6 in the liver of obese rats with sepsis[J]. Chinese Journal of Contemporary Pediatrics. 2018, 20(7): 578-584 https://doi.org/10.7499/j.issn.1008-8830.2018.07.013

参考文献

[1] Juonala M, Magnussen CG, Berenson GS, et al. Childhood adiposity, adult adiposity, and cardiovascular risk factors[J]. N Engl J Med, 2011, 365(20):1876-1885.
[2] Reilly JJ, Kelly J. Long-term impact of overweight and obesity in childhood and adolescence on morbidity and premature mortality in adulthood:systematic review[J]. Int J Obes (Lond), 2011, 35(7):891-898.
[3] Masoodi M, Kuda O, Rossmeisl M, et al. Lipid signaling in adipose tissue:connecting inflammation & metabolism[J]. Biochim Biophys Acta, 2015, 1851(4):503-518.
[4] Cullberg KB, Larsen JØ, Pedersen SB, et al. Effects of LPS and dietary free fatty acids on MCP-1 in 3T3-L1 adipocytes and macrophages in vitro[J]. Nutr Diabetes, 2014, 4:e113.
[5] Li Q, Tian Y, Wang ZF, et al. Involvement of the spinal NALP1 inflammasome in neuropathic pain and aspirin-triggered-15-epilipoxin A4 induced analgesia[J]. Neuroscience, 2013, 254:230-240.
[6] Wu R, Zhou W, Chen S, et al. Lipoxin A4 suppresses the development of endometriosis in an ALX receptor-dependent manner via the p38 MAPK pathway[J]. Br J Pharmacol, 2014, 171(21):4927-4940.
[7] Wu H, Zhao G, Jiang K, et al. Plantamajoside ameliorates lipopolysaccharide-induced acute lung injury via suppressing NF-κB and MAPK activation[J]. Int Immunopharmacol, 2016, 35:315-322.
[8] Guo Z, Hu Q, Xu L, et al. Lipoxin A4 reduces inflammation through formyl peptide receptor 2/p38 MAPK signaling pathway in subarachnoid hemorrhage rats[J]. Stroke, 2016, 47(2):490-497.
[9] 万涛梅, 袁贵强, 王正义, 等. 肥胖对非致死性肺炎小鼠血液生理指标、4种细胞因子和免疫器官指数的影响[J]. 浙江农业学报, 2016, 28(9):1485-1492.
[10] 畅怡, 聂秀红, 蔡彦宁, 等. 脓毒血症对大鼠膈肌Glut-1和Glut-4 mRNA表达的影响[J]. 首都医科大学学报, 2010, 31(5):20-23.
[11] 辛显芳, 高莉莉, 关凤军, 等. 脂氧素A4干预幼年肥胖大鼠血管内皮功能损伤的作用研究[J]. 中国保健营养(下旬刊), 2013, 23(2):896-897.
[12] Börgeson E, Johnson AM, Lee YS, et al. Lipoxin A4 attenuates obesity-induced adipose inflammation and associated liver and kidney disease[J]. Cell Metab, 2015, 22(1):125-137.
[13] 姜红堃, 李雷, 姜红, 等. 肥胖相关性肾小球病小鼠肿瘤坏死因子α表达的变化[J]. 实用儿科临床杂志, 2012, 27(23):21-24.
[14] Rosenfeld ME. Inflammation and atherosclerosis:direct versus indirect mechanisms[J]. Curr Opin Pharmacol, 2013, 13(2):154-160.
[15] Pal D, Dasgupta S, Kundu R, et al. Fetuin-A acts as an endogenous ligand of TLR4 to promote lipid-induced insulin resistance[J]. Nat Med, 2012, 18(8):1279-1285.
[16] Ma C, Jiang Y, Zhang X, et al. Isoquercetin ameliorates myocardial infarction through anti-inflammation and antiapoptosis factor and regulating TLR4-NF-κB signal pathway[J]. Mol Med Rep, 2018, 17(5):6675-6680.
[17] Jiang K, Guo S, Zhang T, et al. Downregulation of TLR4 by miR-181a provides negative feedback regulation to lipopolysaccharide-induced inflammation[J]. Front Pharmacol, 2018, 9:142.
[18] 刁红杰, 鲁燕. Toll样受体4介导的炎症反应与肥胖和胰岛素抵抗的研究进展[J]. 中国糖尿病杂志, 2016, 24(11):1044-1048.
[19] Börgeson E, McGillicuddy FC, Harford KA, et al. Lipoxin A4 attenuates adipose inflammation[J]. FASEB J, 2012, 26(10):4287-4294.
[20] Lv W, Lv C, Yu S, et al. Lipoxin A4 attenuation of endothelial inflammation response mimicking pancreatitis-induced lung injury[J]. Exp Biol Med (Maywood), 2013, 238(12):1388-1395.
[21] Serhan CN, Hamberg M, Samuelsson B. Lipoxins:novel series of biologically active compounds formed from arachidonic acid in human leukocytes[J]. Proc Natl Acad Sci U S A, 1984, 81(17):5335-5339.
[22] Cattaneo F, Parisi M, Ammendola R. Distinct signaling cascades elicited by different formyl peptide receptor 2(FPR2) agonists[J]. Int J Mol Sci, 2013, 14(4):7193-7230.
[23] 邓莉莉, 钟玲, 雷建蓉, 等. 脂氧素A4对横纹肌溶解所致急性肾损伤大鼠肾的保护作用[J]. 细胞与分子免疫学杂志, 2012, 28(9):15-18.
[24] 金胜威, 张力, 姚尚龙, 等. 脂氧素A4对内毒素性肺损伤小鼠的保护作用[J]. 中华急诊医学杂志, 2006, 15(11):7-10.
[25] 孙洪伟, 汪茂名, 张涛, 等. LXA4对ANP诱发SIRS过程中NF-κB、ICAM-1表达的影响[J]. 医学研究杂志, 2012, 41(3):30-33.
[26] Alvarez AM, Mulla MJ, Chamley LW, et al. Aspirin-triggered lipoxin prevents antiphospholipid antibody effects on human trophoblast migration and endothelial cell interactions[J]. Arthritis Rheumatol, 2015, 67(2):488-497.
[27] 徐会会, 高莉莉, 关凤军, 等. 脂氧素A4干预幼年期大鼠代谢综合征的意义[J]. 中华实用儿科临床杂志, 2016, 31(7):522-526.


PDF(1400 KB)
HTML

Accesses

Citation

Detail

段落导航
相关文章

/