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源自中国白酒发酵谷物的新型潜在益生菌:LTJ1/LTJ48在降低尿酸和恢复肠道微生物群以治疗小鼠高尿酸血症中的双重作用

Novel Potential Probiotics from Chinese Baijiu Fermentation Grains: Dual Action of LTJ1/LTJ48 in Uric Acid Reduction and Gut Microbiota Restoration for Hyperuricemia Therapy in Mice.

作者信息

Zhong Feiliang, Feng Xiaomin, Cao Jun, Li Miao, Tian Jianxia, Wang Jiali, Wang Xuefang, Luo Xuegang

机构信息

Key Laboratory of Industrial Fermentation Microbiology of the Ministry of Education, College of Biotechnology, Tianjin University of Science and Technology, Tianjin 300457, China.

出版信息

Nutrients. 2025 Jun 24;17(13):2097. doi: 10.3390/nu17132097.

Abstract

OBJECTIVES

Hyperuricemia (HUA) is a metabolic disorder linked to serious complications, yet current treatments face safety limitations. This study aimed to identify novel probiotic strains from Chinese Baijiu fermentation grains with dual-action mechanisms for HUA management-direct uric acid (UA) reduction and gut microbiota restoration.

METHODS

Two Lactiplantibacillus plantarum strains (LTJ1/LTJ48) were screened for purine/nucleoside degradation using HPLC. Their efficacy was evaluated in HepG2 cells and HUA mice. Key assessments included UA levels, renal/hepatic markers (AST, CRE, BUN), ADA/XOD activity, UA transporter expression (URAT1, GLUT9, ABCG2), and 16S rRNA-based microbiota analysis.

RESULTS

LTJ1/LTJ48 degraded >97% of purines/nucleosides in vitro. In HUA mice, they reduced serum UA by 31.0% (LTJ1) and 51.5% (LTJ48), improved renal/hepatic function, and suppressed ADA activity. They modulated UA transporters and restored gut microbiota.

CONCLUSIONS

LTJ1/LTJ48 exhibit multi-target HUA alleviation via purine degradation, ADA inhibition, UA transporter regulation, and microbiota remodeling, offering a safer probiotic-based alternative to conventional therapies. Their translational potential warrants further clinical exploration.

摘要

目的

高尿酸血症(HUA)是一种与严重并发症相关的代谢紊乱疾病,但目前的治疗方法存在安全性限制。本研究旨在从中国白酒发酵谷物中鉴定出具有双重作用机制的新型益生菌菌株,用于管理高尿酸血症——直接降低尿酸(UA)水平并恢复肠道微生物群。

方法

使用高效液相色谱法筛选两株植物乳杆菌(LTJ1/LTJ48)对嘌呤/核苷的降解能力。在HepG2细胞和高尿酸血症小鼠中评估它们的功效。关键评估指标包括尿酸水平、肾/肝标志物(AST、CRE、BUN)、ADA/XOD活性、尿酸转运蛋白表达(URAT1、GLUT9、ABCG2)以及基于16S rRNA的微生物群分析。

结果

LTJ1/LTJ48在体外降解了>97%的嘌呤/核苷。在高尿酸血症小鼠中,它们使血清尿酸分别降低了31.0%(LTJ1)和51.5%(LTJ48),改善了肾/肝功能,并抑制了ADA活性。它们调节尿酸转运蛋白并恢复肠道微生物群。

结论

LTJ1/LTJ48通过嘌呤降解、ADA抑制、尿酸转运蛋白调节和微生物群重塑表现出多靶点缓解高尿酸血症的作用,为传统疗法提供了一种更安全的基于益生菌的替代方案。它们的转化潜力值得进一步的临床探索。

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