肠道微生物组和代谢物介导急性肾损伤后小鼠热量限制的益处。

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xue-Xue Zhu , Xiao Fu , Xin-Yu Meng , Jia-Bao Su , Guan-Li Zheng , An-Jing Xu , Guo Chen , Yuan Zhang , Yao Liu , Xiao-Hui Hou , Hong-Bo Qiu , Qing-Yi Sun , Jin-Yi Hu , Zhuo-Lin Lv , Yao Wang , Hai-Bin Jiang , Neng Bao , Zhi-Jun Han , Qing-Bo Lu , Hai-Jian Sun
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引用次数: 0

摘要

肠道微生物组在急性肾损伤(AKI)中的作用日益得到认可。研究表明,热量限制(CR)可增强啮齿类动物肾脏对缺血/再灌注损伤的抵抗力。然而,肠道微生物群是否介导了热量限制对肾脏缺血/再灌注诱导损伤(IRI)的保护作用尚不清楚。在这里,我们发现 CR 可改善 IRI 引起的肾功能障碍、氧化应激、细胞凋亡和炎症,同时增强肠道屏障功能。此外,肠道微生物群耗竭阻碍了 CR 对 AKI 小鼠的有利影响。16S rRNA和代谢组学分析表明,CR富集了肠道共生菌金丝桃菌(Parabacteroides goldsteinii,P. goldsteinii),并上调了血清代谢物十二氟戊烷的水平。在 AKI 小鼠的肠道中定植金氏副杆菌和口服十二氟戊烷显示出与 CR 类似的有益效果。RNA测序和实验数据显示,十二氟戊烷通过拮抗氧化猝灭和NFκB诱导的NLRP3炎性体激活,保护AKI诱导的肾损伤。此外,我们还筛选并发现,Hamaudol 可通过促进金黄色葡萄球菌的生长来改善肾功能不全。我们的研究结果揭示了肠道微生物群P. goldsteinii和血清代谢物十二氟戊烷在CR对AKI的益处中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiome and metabolites mediate the benefits of caloric restriction in mice after acute kidney injury
The role of gut microbiome in acute kidney injury (AKI) is increasing recognized. Caloric restriction (CR) has been shown to enhance the resistance to ischemia/reperfusion injury to the kidneys in rodents. Nonetheless, it is unknown whether intestinal microbiota mediated CR protection against ischemic/reperfusion-induced injury (IRI) in the kidneys. Herein, we showed that CR ameliorated IRI-elicited renal dysfunction, oxidative stress, apoptosis, and inflammation, along with enhanced intestinal barrier function. In addition, gut microbiota depletion blocked the favorable effects of CR in AKI mice. 16S rRNA and metabolomics analysis showed that CR enriched the gut commensal Parabacteroides goldsteinii (P. goldsteinii) and upregulated the level of serum metabolite dodecafluorpentan. Intestinal colonization of P. goldsteinii and oral administration of dodecafluorpentan showed the similar beneficial effects as CR in AKI mice. RNA sequencing and experimental data revealed that dodecafluorpentan protected against AKI-induced renal injury by antagonizing oxidative burst and NFκB-induced NLRP3 inflammasome activation. In addition, we screened and found that Hamaudol improved renal insufficiency by boosting the growth of P. goldsteinii. Our results shed light on the role of intestinal microbiota P. goldsteinii and serum metabolites dodecafluorpentan in CR benefits to AKI.
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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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