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志贺田菌株对易患肾病小鼠的肾脏保护和免疫调节作用。

Renal protective and immunoregulatory effects of strain Shirota in nephropathy-prone mice.

作者信息

Chan Chun-Wai, Chen Yu-Ting, Lin Bi-Fong

机构信息

Department of Biochemical Science and Technology, College of Life Science, National Taiwan University, Taipei, Taiwan.

出版信息

Front Nutr. 2024 Aug 23;11:1438327. doi: 10.3389/fnut.2024.1438327. eCollection 2024.

Abstract

INTRODUCTION

The incidence of severe acute kidney injury (AKI) is considerably high worldwide. A previous study showed that gut microbial dysbiosis was a hallmark of AKI in mice. Whether the probiotic strain Shirota (LcS) plays a role in kidney disease, particularly AKI, remains unclear.

METHODS

To investigate the effects of LcS on kidney injury, tubule-specific conditional von Hippel-Lindau gene-knockout C57BL/6 mice ( mice) were supplemented without (Ctrl) or with probiotics (LcS) in Experiment 1, and their lifespan was monitored. Additionally, the mice were supplemented without (Ctrl and AA) or with probiotics (LcS and LcS + AA) in Experiment 2. Probiotic LcS (1 × 10 colony-forming units) was supplemented once daily. After 4 weeks of LcS supplementation, AA and LcS + AA mice were administered aristolochic acid (AA; 4 mg/kg body weight/day)-containing purified diet for 2 weeks to induce AA nephropathy before sacrifice.

RESULTS

Supplementation of LcS significantly prolonged the lifespan of mice, suggesting a potential renal protective effect. AA induced-nephropathy increased not only the indicators of renal dysfunction and injury, including urinary protein and kidney injury molecule (KIM)-1, serum blood urea nitrogen (BUN) and creatinine, but also serum interleukin (IL)-6 levels, renal macrophage infiltrations, and pathological lesions in mice. LcS supplementation significantly reduced urinary protein and KIM-1 levels, serum BUN and IL-6 levels, and renal M1 macrophages, tissue lesions, and injury scores. We also found that LcS maintained gut integrity under AA induction and increased intestinal lamina propria dendritic cells. Furthermore, LcS significantly reduced pro-inflammatory IL-17A and upregulated anti-inflammatory IL-10 production by immune cells from intestinal Peyer's patches (PP) or mesenteric lymph nodes (MLN), and significantly increased IL-10 and reduced IL-6 production by splenocytes.

CONCLUSION

Prior supplementation with probiotic LcS significantly alleviated the severity of renal injury. This renal protective effect was partially associated with the enhancements of intestinal and systemic anti-inflammatory immune responses, suggesting that LcS-induced immunoregulation might contribute to its renal protective effects.

摘要

引言

在全球范围内,严重急性肾损伤(AKI)的发病率相当高。先前的一项研究表明,肠道微生物群失调是小鼠急性肾损伤的一个标志。益生菌株LcS是否在肾脏疾病尤其是急性肾损伤中发挥作用仍不清楚。

方法

在实验1中,为了研究LcS对肾损伤的影响,对肾小管特异性条件性冯·希佩尔-林道基因敲除的C57BL/6小鼠(小鼠)分别不补充(对照组)或补充益生菌(LcS),并监测它们的寿命。此外,在实验2中,对小鼠分别不补充(对照组和AA)或补充益生菌(LcS和LcS+AA)。每天补充一次益生菌LcS(1×10菌落形成单位)。在补充LcS 4周后,对AA和LcS+AA小鼠给予含马兜铃酸(AA;4mg/kg体重/天)的纯化饮食2周以诱导AA肾病,然后处死。

结果

补充LcS显著延长了小鼠的寿命,表明其具有潜在的肾脏保护作用。AA诱导的肾病不仅增加了肾功能障碍和损伤的指标,包括尿蛋白和肾损伤分子(KIM)-1、血清血尿素氮(BUN)和肌酐,还增加了小鼠血清白细胞介素(IL)-6水平、肾巨噬细胞浸润和病理损伤。补充LcS显著降低了尿蛋白和KIM-1水平、血清BUN和IL-6水平,以及肾M1巨噬细胞、组织损伤和损伤评分。我们还发现,LcS在AA诱导下维持肠道完整性并增加肠固有层树突状细胞。此外,LcS显著降低促炎细胞因子IL-17A,并上调来自肠道派尔集合淋巴结(PP)或肠系膜淋巴结(MLN)的免疫细胞产生的抗炎细胞因子IL-10,并且显著增加脾细胞产生的IL-10并降低IL-6。

结论

预先补充益生菌LcS显著减轻了肾损伤的严重程度。这种肾脏保护作用部分与肠道和全身抗炎免疫反应的增强有关,表明LcS诱导的免疫调节可能有助于其肾脏保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b41/11389617/29acbd06a647/fnut-11-1438327-g001.jpg

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