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生物活性铱纳米酶对小鼠高原相关缺氧诱导肾损伤的保护作用

Protective effect of bioactive iridium nanozymes on high altitude-related hypoxia-induced kidney injury in mice.

作者信息

Wang Yujing, Shi Meijun, Chu Zongtang, Yan Xinlin, You Guoxing, Chen Gan, Zhou Hong

机构信息

Institute of Health Service and Transfusion Medicine, Academy of Military Medical Sciences, Beijing, China.

Key Laboratory of Pollution Ecology and Environmental Engineering, Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang, China.

出版信息

Front Pharmacol. 2023 Feb 20;14:1115224. doi: 10.3389/fphar.2023.1115224. eCollection 2023.

Abstract

High altitude-related hypoxia-induced organ damage significantly impacts people who are exposed to acute high-altitude environment. At present, kidney injury still lacks effective treatment strategies. Iridium nanozymes (Ir-NPs) are a nanomaterial with various enzymatic activities and are expected to be used in kidney injury treatment. In this study, we simulated a high-altitude environment (6000 m) to induce a kidney injury model, and explored the therapeutic effect of Ir-NPs in mice with kidney injury in this environment. Changes in the microbial community and metabolites were analyzed to explore the possible mechanism underlying the improvement of kidney injury during acute altitude hypoxia in mice treated with Ir-NPs. It was discovered that plasma lactate dehydrogenase and urea nitrogen levels were considerably increased in mice exposed to acute altitude hypoxia compared to mice in a normal oxygen environment. Furthermore, there was a substantial increase in IL-6 expression levels in hypoxic mice; contrastingly, Ir-NPs decreased IL-6 expression levels, reduced the levels of succinic acid and indoxyl sulfate in the plasma and kidney pathological changes caused by acute altitude hypoxia. Microbiome analysis showed that bacteria, such as Lachnospiraceae_UCG_006 predominated in mice treated with Ir-NPs. Correlation analysis of the physiological, biochemical, metabolic, and microbiome-related parameters showed that Ir-NPs could reduce the inflammatory response and protect kidney function under acute altitude hypoxia, which may be related to intestinal flora distribution regulation and plasma metabolism in mice. Therefore, this study provides a novel therapeutic strategy for hypoxia-related kidney injury, which could be applied to other hypoxia-related diseases.

摘要

高原相关的缺氧诱导器官损伤对暴露于急性高原环境的人有显著影响。目前,肾损伤仍缺乏有效的治疗策略。铱纳米酶(Ir-NPs)是一种具有多种酶活性的纳米材料,有望用于肾损伤治疗。在本研究中,我们模拟高原环境(6000米)诱导肾损伤模型,并探讨Ir-NPs对该环境下肾损伤小鼠的治疗效果。分析微生物群落和代谢产物的变化,以探索Ir-NPs治疗的小鼠在急性高原缺氧期间肾损伤改善的潜在机制。结果发现,与正常氧环境中的小鼠相比,暴露于急性高原缺氧的小鼠血浆乳酸脱氢酶和尿素氮水平显著升高。此外,缺氧小鼠中IL-6表达水平大幅增加;相反,Ir-NPs降低了IL-6表达水平,降低了血浆中琥珀酸和硫酸吲哚酚的水平以及急性高原缺氧引起的肾脏病理变化。微生物组分析表明,在接受Ir-NPs治疗的小鼠中,诸如毛螺菌科_UCG_006等细菌占主导。对生理、生化、代谢和微生物组相关参数的相关性分析表明,Ir-NPs在急性高原缺氧条件下可减轻炎症反应并保护肾功能,这可能与小鼠肠道菌群分布调节和血浆代谢有关。因此,本研究为缺氧相关肾损伤提供了一种新的治疗策略,可应用于其他缺氧相关疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d58/9986433/07fdf6bc4e3f/fphar-14-1115224-g001.jpg

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