Lactulose, a Disaccharide Prebiotic, Improves the Gut-Kidney Axis via Enhancement of Akkermansia Muciniphila Production

乳果糖 生物 生物化学 药理学 口服 微生物学 内科学 代谢物 双糖 肾功能 肾脏疾病 生物利用度 新陈代谢 肠道菌群 立体化学 细菌 医学
作者
Miyu Sueyoshi,Hiroshi Watanabe,Moritaka Goto,Sato Takao,Mai Hashimoto,Mayu Oki,Ebenezer Ofori-Attah,Takehiro Nakano,Hitoshi Maeda,Motoko Tanaka,Kazutaka Matsushita,Hideaki Jinnouchi,Toru Maruyama,Daisuke Kadowaki
出处
期刊:Kidney360 [American Society of Nephrology (ASN)]
标识
DOI:10.34067/kid.0000001040
摘要

Background: Recently, we reported that lactulose, a synthetic disaccharide used to treat chronic constipation, improved the gut-renal axis in mice with adenine-induced CKD. However, the underlying mechanism remains unclear. Akkermansia muciniphila (AKK), a next-generation probiotic, mitigates multi-organ dysfunction, including kidney impairment, by modulating intestinal health. This study aimed to investigate whether lactulose induces AKK proliferation and contributes to its renoprotective effects. Methods: CKD was induced in 7-week-old male C57BL/6N mice by administering 0.2% adenine for four weeks. After adenine discontinuation, the CKD mice received oral administration of lactulose (7.5% or 10%) or AKK (2 × 10 CFU/mouse) for three weeks. Intestinal permeability was assessed by measuring plasma levels of fluorescent probe for fluorescein isothiocyanate-dextran (4 kDa) and lipopolysaccharides. The composition of the gut microbiota was analyzed using 16S rRNA sequencing. Results: Lactulose administration significantly ameliorated renal impairment in CKD mice and improved intestinal barrier integrity by increasing intestinal mucosal thickness. Additionally, lactulose modulated CKD-induced gut dysbiosis, thereby altering microbiota diversity and composition with a notable increase in AKK abundance. This was further supported by in vitro findings that demonstrated a significant increase in AKK proliferation upon lactulose treatment. Similar to lactulose, oral administration of AKK (both live and pasteurized forms) for three weeks attenuated renal damage in CKD mice. Moreover, both forms of AKK significantly improved intestinal barrier function by enhancing mucosal integrity. Conclusions: Our findings suggest that lactulose functions as an in vivo AKK inducer, exerting renoprotective effects by improving intestinal barrier function in CKD. These results highlight the potential of lactulose as a prebiotic therapeutic agent for CKD management.

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