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基于化橘红多糖富集的拟杆菌属可通过抑制脂多糖相关的 PI3K-Akt 信号通路改善结肠炎。

Parabacteroides goldsteinii enriched by Pericarpium Citri Reticulatae 'Chachiensis' polysaccharides improves colitis via the inhibition of lipopolysaccharide-involved PI3K-Akt signaling pathway.

机构信息

Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Pharmacy and Food Engineering, Wuyi University, Jiangmen 529020, PR China; International Healthcare Innovation Institute (Jiangmen), Jiangmen 529040, PR China.

Guangdong Xinbaotang Biotechnology Co. Ltd., Jiangmen 529100, PR China; Guangdong Xinbaotang Pharmaceutical Co. Ltd., Jiangmen 529100, PR China.

出版信息

Int J Biol Macromol. 2024 Oct;277(Pt 1):133726. doi: 10.1016/j.ijbiomac.2024.133726. Epub 2024 Jul 31.

DOI:10.1016/j.ijbiomac.2024.133726
PMID:39084973
Abstract

Epidemiological and preclinical studies have indicated a factual association between gut microbiota dysbiosis and high incidence of colitis. Dietary polysaccharides can specifically shift the composition of gut microbiome response to colitis. Here we validated the preventive role of polysaccharides from Pericarpium Citri Reticulatae 'Chachiensis' (PCRCP), a well-known traditional Chinese medicine, in colitis induced by dextrose sodium sulfate (DSS) in both rats and mice. We found that treatment with PCRCP not only significantly reduced DSS-induced colitis via down-regulating colonic inflammatory signaling pathways including PI3K-Akt, NLRs and NF-κB, but also enhanced colonic barrier integrity in rats. These protective activities of PCRCP against DSS-induced injuries in rats were in part due to the modulation of the gut microbiota revealed by both broad-spectrum antibiotic (ABX)-deleted bacterial and non-oral treatments. Furthermore, the improvement of PCRCP on colitis was impaired by intestinal neomycin-sensitive bacteria in DSS-exposed mice. Specifically, in vivo and in vitro treatment with PCRCP led to a highly sensible enrichment in the gut commensal Parabacteroides goldsteinii. Administration of Parabacteroides goldsteinii significantly alleviated typical symptoms of colitis and suppressed the activation of PI3K-Akt-involved inflammatory response in DSS-exposed mice. The anti-colitic effects of Parabacteroides goldsteinii were abolished after the activation of PI3K-Akt signaling pathway by lipopolysaccharide treatment in mice exposed to DSS. This study provides new insights into an anti-colitic mechanism driven by PCRCP and highlights the potential prebiotic of Parabacteroides goldsteinii for the prevention of ulcerative colitis.

摘要

流行病学和临床前研究表明,肠道微生物群落失调与结肠炎高发之间存在实际关联。膳食多糖可以特异性地改变肠道微生物群落对结肠炎的反应组成。在这里,我们验证了一种众所周知的中药——化橘红(PCRCP)多糖在葡聚糖硫酸钠(DSS)诱导的大鼠和小鼠结肠炎中的预防作用。我们发现,PCRCP 治疗不仅通过下调包括 PI3K-Akt、NLRs 和 NF-κB 在内的结肠炎症信号通路,显著减轻 DSS 诱导的结肠炎,而且还增强了大鼠的结肠屏障完整性。PCRCP 对大鼠 DSS 诱导损伤的这些保护作用部分归因于广谱抗生素(ABX)缺失细菌和非口服治疗所揭示的肠道微生物群落的调节。此外,肠道新霉素敏感细菌在 DSS 暴露的小鼠中削弱了 PCRCP 改善结肠炎的作用。具体而言,体内和体外用 PCRCP 处理导致肠道共生拟杆菌(Parabacteroides goldsteinii)高度敏感富集。在 DSS 暴露的小鼠中,给予拟杆菌(Parabacteroides goldsteinii)可显著缓解典型的结肠炎症状,并抑制 PI3K-Akt 参与的炎症反应的激活。在 DSS 暴露的小鼠中,用脂多糖处理激活 PI3K-Akt 信号通路后,拟杆菌(Parabacteroides goldsteinii)的抗结肠炎作用被消除。本研究为 PCRCP 驱动的抗结肠炎机制提供了新的见解,并强调了拟杆菌(Parabacteroides goldsteinii)作为预防溃疡性结肠炎的潜在益生元的潜力。

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