Zn2+ regulates human oxalate metabolism by manipulating oxalate decarboxylase to treat calcium oxalate stones

草酸盐 草酸钙 肾结石 化学 生物化学 微生物学 内科学 医学 生物 无机化学
作者
Fang Wu,Yuanyuan Cheng,Jianfu Zhou,Xuehua Liu,Rongwu Lin,Songtao Xiang,Zhongqiu Liu,Caiyan Wang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:234: 123320-123320 被引量:16
标识
DOI:10.1016/j.ijbiomac.2023.123320
摘要

A high concentration of oxalate is associated with an increased risk of kidney calcium oxalate (CaOx) stones, and the degradation of exogenous oxalate mostly depends on oxalate-degrading enzymes from the intestinal microbiome. We found that zinc gluconate supplement to patients with CaOx kidney stones could significantly improve the abundance of oxalate metabolizing bacteria in humans through clinical experiments on patients also subjected to antibiotic treatment. The analysis of clinical samples revealed that an imbalance of Lactobacillus and oxalate decarboxylase (OxDC) was involved in the formation of CaOx kidney stones. Then, we identified that Zn2+ could be used as an external factor to improve the activity of OxDC and promote Lactobacillus in the intestinal flora, and this treatment achieved a therapeutic effect on rats with stones aggravated by antibiotics. Finally, by analyzing the three-dimensional structure of OxDC and completing in vitro experiments, we propose a model of the Zn2+-induced reduction of CaOx kidney stone symptoms in rats by increasing the metabolism of oxalate through the positive effects of Zn2+ on Lactobacillus and OxDC.
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