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益生菌混合物通过调节孕烷X受体-应激活化蛋白激酶途径增强屏障功能,以改善坏死性小肠结肠炎。

Probiotics mixture reinforces barrier function to ameliorate necrotizing enterocolitis by regulating PXR-JNK pathway.

作者信息

Zhao Xiuhao, Zhou Jin, Liang Wenhua, Sheng Qingfeng, Lu Li, Chen Tong, Chen Jianglong, Tan Kezhe, Lv Zhibao

机构信息

Department of General Surgery, Shanghai Children's Hospital, Shanghai Jiao Tong University, 355 Luding Road, Putuo, Shanghai, China.

Shanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Cell Biosci. 2021 Jan 19;11(1):20. doi: 10.1186/s13578-021-00530-7.

Abstract

BACKGROUND

Intestinal dysbiosis is believed to be one of the factors inducing neonatal necrotizing enterocolitis (NEC). Probiotics have been employed to treat NEC in a number of animal experiments and clinical trials, and some significant benefits of utilizing probiotics for the prevention or alleviation of NEC have been confirmed. However, the mechanism underlying the efficacy of probiotics in treating NEC has not been elucidated.

RESULTS

Impairment of the intestinal barrier, which was characterized by the decreased expression of tight junction components, was observed in the pathogenesis of NEC. The probiotic mixture alleviated this intestinal damage by enhancing the function of the barrier. Meanwhile, the probiotics remodeled the composition of the intestinal microbiota in NEC mice. Furthermore, increased expression of the pregnane X receptor (PXR) was observed after treatment with the probiotic mixture, and PXR overexpression in Caco-2 cells protected the barrier from lipopolysaccharide (LPS) damage. Further research showed that PXR could inhibit the phosphorylation of c-Jun N-terminal kinase (JNK) and could increase the expression of tight junction components.

CONCLUSIONS

Our study confirmed that probiotics could ameliorate intestinal lesions by enhancing the function of the mucosal barrier. Specifically, probiotics may target PXR, which may subsequently enhance the expression of tight junction components by inhibiting the phosphorylation of JNK and enhance the function of the barrier.

摘要

背景

肠道菌群失调被认为是诱发新生儿坏死性小肠结肠炎(NEC)的因素之一。在一些动物实验和临床试验中,益生菌已被用于治疗NEC,并且利用益生菌预防或减轻NEC的一些显著益处已得到证实。然而,益生菌治疗NEC的疗效背后的机制尚未阐明。

结果

在NEC的发病机制中观察到肠道屏障受损,其特征为紧密连接成分的表达降低。益生菌混合物通过增强屏障功能减轻了这种肠道损伤。同时,益生菌重塑了NEC小鼠肠道微生物群的组成。此外,用益生菌混合物治疗后观察到孕烷X受体(PXR)的表达增加,并且Caco-2细胞中PXR的过表达保护屏障免受脂多糖(LPS)损伤。进一步的研究表明,PXR可以抑制c-Jun氨基末端激酶(JNK)的磷酸化,并可以增加紧密连接成分的表达。

结论

我们的研究证实,益生菌可以通过增强黏膜屏障功能来改善肠道病变。具体而言,益生菌可能靶向PXR,PXR随后可能通过抑制JNK的磷酸化来增强紧密连接成分的表达并增强屏障功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f6/7824920/d45af7eac568/13578_2021_530_Fig1_HTML.jpg

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