失调
肾脏疾病
肠道菌群
微生物群
发病机制
肾
尿毒症
医学
免疫学
肾功能
肾病
氧化三甲胺
生物
内科学
生物信息学
内分泌学
糖尿病
三甲胺
生物化学
作者
Fariba Mahmoodpoor,Yalda Rahbar Saadat,Abolfazl Barzegari,Mohammadreza Ardalan,Sepideh Zununi Vahed
标识
DOI:10.1016/j.biopha.2017.06.066
摘要
Chronic kidney diseases (CKDs) are a global health problem. Besides diverse leading reasons in initiation and progression of CKDs, it is evident that they might largely originate from changes in the gut microbial community (microbiota). Mounting evidence indicates that a bidirectional relationship exists between host and microbiome in humans and animals with CKDs. Changes in the microbiota composition and structure (dysbiosis) produce excessive amounts of uremic toxins (e.g. indoxyl sulfate, p-cresyl sulfate and trimethylamine-N-oxide) but less reno-protective metabolites that are implicated in oxidative stress, uremia, inflammation, deterioration of kidney function, kidney diseases progression, a higher prevalence of cardiovascular risk, and mortality in patients with CKD. The present review focuses on the pathogenic association between gut microbiota and kidney diseases like CKD, IgA nephropathy, and kidney stone disease. Certainly, novel insights into the impact of the gut microbiota in kidney diseases can be helpful to develop therapeutic strategies in order to avoid and/or treat aforementioned conditions.
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