丁香能有效改善小鼠高尿酸血症和高尿酸血症引起的肾损伤

IF 6.2 Q1 AGRICULTURE, MULTIDISCIPLINARY Journal of Agriculture and Food Research Pub Date : 2025-04-01 Epub Date: 2025-02-25 DOI:10.1016/j.jafr.2025.101760
Fang Wang , Lin Fang , Jin-Juan Zhang , Qian Wang , Ya Wang , Qiong Fu , Yan Hong , Yan-Yan Gao , Xiao-Li Guo , Jing Li , Xue-Long Yan , Guo-Bo Xu , Xing-Jiang Liao , Xiang Fang , Shang-Gao Liao
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引用次数: 0

摘要

丁香(Syzygium aromaticum)的干花蕾,是一种用于各种烹饪传统的全球香料。本研究采用高尿酸血症小鼠模型研究丁香水提取物(CWE)的抗高尿酸血症(anti-HUA)作用及其机制,并采用器官系数和组织学评估来确定其安全性。Western blot、RT-qPCR和转录组学分析揭示了相关的蛋白、rna和信号通路。结果表明,极低剂量丁香水提取物可显著降低HUA小鼠血清尿酸(UA)水平,且对脏器无明显毒性,显著减轻HUA所致肾损害。Western blotting分析显示,黄嘌呤氧化酶(XOD)、尿酸转运蛋白1 (URAT1)、葡萄糖转运蛋白9 (GLUT9)、单羧酸转运蛋白9 (MCT9)的表达量显著降低,肾有机阴离子转运蛋白1 (OAT1)、3 (OAT3)和ATP转运蛋白G2 (ABCG2)的表达量显著升高。转录组学分析显示,CWE逆转了HUA诱导的肾内38个差异表达的关键基因。炎症因子及其转录因子在细胞因子-细胞因子受体相互作用信号通路中的表达减少也被观察到。CWE降低UA的机制包括抑制XOD抑制UA的合成;降低URAT1、GLUT9和MCT9的表达以减少UA的重吸收;增强ABCG2、OAT1和OAT3的表达,增加UA的消除。此外,CWE能够通过调节细胞因子-细胞因子受体相互作用的信号通路来减轻hua诱导的肾损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The spice clove effectively ameliorated hyperuricemia and hyperuricemia-induced kidney injury in mice
Clove, the dried flower bud of Syzygium aromaticum, is a global spice used in various culinary traditions. In the present study, the antihyperuricemic (anti-HUA) effect of a clove water extract (CWE) and its mechanism were investigated using a hyperuricemic (HUA) mouse model, with organ coefficients and histological assessments employed to determine its safety profile. Western blot, RT-qPCR and transcriptomic analysis were conducted to uncover the proteins, RNAs and signalling pathways involved. The results showed that a very low dose of clove water extract could significantly lower serum uric acid (UA) levels in HUA mice with no overt toxicity to the organs and markedly attenuated HUA-induced renal damage. Western blotting analysis revealed that the expression levels of xanthine oxidase (XOD), urate transporter 1 (URAT1), glucose transporter 9 (GLUT9), and monocarboxylate transporter 9 (MCT9) were substantially decreased, whereas those of renal organic anion transporters 1 (OAT1) and 3 (OAT3) and ATP transporter G2 (ABCG2) were notably increased. Transcriptomic analysis revealed that CWE reversed 38 differentially expressed key genes within the kidney induced by HUA. A reduction in the expression of inflammatory cytokines and their transcription factors in the cytokine‒cytokine receptor interaction signalling pathway was also observed. The UA-lowering mechanism of CWE involved suppressing XOD to curtail UA synthesis; lowering the expression of URAT1, GLUT9, and MCT9 to diminish UA reabsorption; and enhancing the expression of ABCG2, OAT1, and OAT3 to increase UA elimination. Additionally, CWE is capable of mitigating HUA-induced kidney injury through modulating the cytokine‒cytokine receptor interaction signalling pathway.
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来源期刊
CiteScore
5.40
自引率
2.60%
发文量
193
审稿时长
69 days
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