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首页> 外文期刊>Cytokine >Dehydroepiandrosterone resisted E. Coli O157:H7-induced inflammation via blocking the activation of p38 MAPK and NF-kappa B pathways in mice
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Dehydroepiandrosterone resisted E. Coli O157:H7-induced inflammation via blocking the activation of p38 MAPK and NF-kappa B pathways in mice

机译:通过阻断小鼠的P38 MAPK和NF-Kappa B途径的激活,脱氢硫磺酸酯酮抗大肠杆菌O157:H7诱导的炎症

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摘要

Dehydroepiandrosterone (DHEA), a critical metabolite in cholesterol metabolism, can regulate the inflammatory responses in humans or animals. However, the precise mechanisms of these beneficial actions remains poorly understood. Present study aims to clarify the anti-inflammatory function of DHEA and its possible mechanisms in the E. coli O157:H7-stimulated mice. The results indicated that DHEA reduced the mortality of mice and bacterial concentration in the peritoneal fluid in the E. coli-stimulated mice. DHEA increased the spleen index, the activity of lactate dehydrogenase and acid phosphatase; while it decreased the nitric oxide (NO) content and inducible nitric oxide synthase (iNOS) activity in mice. The mRNA levels of tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6) and interferon gamma (IFN-gamma) were decreased, whereas the interleukin-4 (IL-4) and interleukin-10 (IL-10) mRNA levels were increased in the E. coli-stimulated mice treated with DHEA. Moreover, DHEA treatment reversed the increasing of IFN-gamma/IL-4 ratio in mice caused by E. coli infection. Importantly, DHEA blocked the nuclear translocation of p65 through down-regulation the IKB-alpha protein phosphorylation level in the mice stimulated with E. coli O157:H7. No statically changes were showed on the phospho (p)-ERK1/2 and p-JNK1/2 protein level, while DHEA significantly suppressed the p-p38 protein level in mice. The above results indicated that DHEA alleviated inflammatory responses by suppressing NO secretion and promoting Th2-associated anti-inflammatory cytokines production in mice; and this action might relate to the blocking of p38 MAPK and NF-kappa B signaling pathways activation. All the above results provide substantial information for understanding the anti-inflammatory function of DHEA and further support it as a potential immunomodulatory in prevention inflammatory and bacterial infection diseases.
机译:脱氢哌啶(DHEA),胆固醇代谢中临界代谢物,可以调节人类或动物的炎症反应。然而,这些有益行动的确切机制仍然明白很差。目前的研究旨在阐明DHEA的抗炎功能及其在大肠杆菌O157:H7刺激的小鼠中可能的机制。结果表明,DHEA在大肠杆菌刺激的小鼠中降低了腹膜液中的小鼠和细菌浓度的死亡率。 DHEA增加了脾指数,乳酸脱氢酶和酸性磷酸酶的活性;虽然它在小鼠中降低了一氧化氮(NO)含量和诱导的一氧化氮合酶(InOS)活性。肿瘤坏死因子-α(TNF-α),白细胞介素-1β(IL-1β),白细胞介素-6(IL-6)和干扰素γ(IFN-Gamma)的mRNA水平降低,而白细胞介素-4 (IL-4)和白细胞介素-10(IL-10)MRNA水平在用DHEA处理的大肠杆菌刺激的小鼠中增加。此外,DHEA治疗逆转了大肠杆菌感染引起的小鼠IFN-Gamma / IL-4的增加。重要的是,DHEA通过下调核转位P65的核转位,通过大肠杆菌O157:H7刺激的小鼠中的小鼠IKB-α蛋白磷酸化水平。在磷酸(P)-ErK1 / 2和P-JNK1 / 2蛋白水平上没有显示静态变化,而DHEA显着抑制小鼠的P-P38蛋白质水平。上述结果表明,DHEA通过抑制小鼠中没有分泌并促进TH2相关的抗炎细胞因子产生而缓解炎症反应;此动作可能涉及P38 MAPK和NF-KAPPA信用通信路径激活的阻塞。所有上述结果都提供了了解DHEA的抗炎功能的大量信息,并进一步支持其作为预防炎症和细菌感染疾病的潜在免疫调节。

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