Anti-inflammatory Effects of the Octapeptide NAP in Human Microbiota-Associated Mice Suffering from Subacute Ileitis.

Ulrike Escher, Eliezer Giladi, Ildikò R Dunay, Stefan Bereswill, Illana Gozes, Markus M Heimesaat
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引用次数: 16

Abstract

The octapeptide NAP is well known for its neuroprotective properties. We here investigated whether NAP treatment could alleviate pro-inflammatory immune responses during experimental subacute ileitis. To address this, mice with a human gut microbiota were perorally infected with one cyst of Toxoplasma gondii (day 0) and subjected to intraperitoneal synthetic NAP treatment from day 1 until day 8 postinfection (p.i.). Whereas placebo (PLC) control animals displayed subacute ileitis at day 9 p.i., NAP-treated mice exhibited less pronounced pro-inflammatory immune responses as indicated by lower numbers of intestinal mucosal T and B lymphocytes and lower interferon (IFN)-γ concentrations in mesenteric lymph nodes. The NAP-induced anti-inflammatory effects were not restricted to the intestinal tract but could also be observed in extra-intestinal including systemic compartments, given that pro-inflammatory cytokines were lower in liver, kidney, and lung following NAP as compared to PLC application, whereas at day 9 p.i., colonic and serum interleukin (IL)-10 concentrations were higher in the former as compared to the latter. Remarkably, probiotic commensal bifidobacterial loads were higher in the ileal lumen of NAP as compared to PLC-treated mice with ileitis. Our findings thus further support that NAP might be regarded as future treatment option directed against intestinal inflammation.

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八肽NAP对患有亚急性Ileitis的人类微生物群相关小鼠的抗炎作用。
八肽NAP以其神经保护特性而闻名。我们在这里研究了NAP治疗是否可以减轻实验性亚急性回肠炎期间的促炎免疫反应。为了解决这一问题,将具有人类肠道微生物群的小鼠全程感染一个弓形虫囊肿(第0天),并从感染后第1天到第8天(p.i.)接受腹膜内合成NAP治疗。而安慰剂(PLC)对照动物在p.i.第9天表现出亚急性回肠炎。,NAP处理的小鼠表现出不太明显的促炎免疫反应,表现为肠粘膜T和B淋巴细胞数量减少以及肠系膜淋巴结中干扰素(IFN)-γ浓度降低。NAP诱导的抗炎作用不仅限于肠道,还可以在肠外(包括全身)区室中观察到,因为与PLC应用相比,NAP后肝、肾和肺中的促炎细胞因子较低,而在第9天。,结肠和血清白细胞介素(IL)-10浓度前者高于后者。值得注意的是,与PLC治疗的患有回肠炎的小鼠相比,NAP回肠腔内的益生菌共生双歧杆菌负荷更高。因此,我们的研究结果进一步支持NAP可能被视为未来针对肠道炎症的治疗选择。
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