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金橘类黄酮通过上调微小RNA-145抑制NLRP3炎性小体的激活,从而减轻载脂蛋白E基因敲除小鼠的动脉粥样硬化。

Kumquat Flavonoids Attenuate Atherosclerosis in ApoE Mice by Inhibiting the Activation of NLRP3 Inflammasome through Upregulating MicroRNA-145.

作者信息

Cao Linhai, Chen Junli, Ni Hongxia, Gong Xiaoxiao, Zang Ziyan, Chang Hui

机构信息

College of Food Science, Southwest University, Chongqing 400715, China.

State Key Laboratory of Space Medicine, China Astronaut Research and Training Center, Beijing 100094, China.

出版信息

J Agric Food Chem. 2025 Jul 9;73(27):16879-16889. doi: 10.1021/acs.jafc.5c00295. Epub 2025 Apr 22.

Abstract

Atherosclerosis (AS) is widely recognized as a consequence of chronic inflammation, with the nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome playing a pivotal role in mediating this inflammatory response. Kumquat flavonoids (KFs), the primary active ingredients in kumquat, have demonstrated potential in modulating inflammation and may help prevent AS. Herein, this study aimed to explore the protective effects and underlying mechanisms of KFs on AS using an ApoE mouse model fed a high-fat/cholesterol diet (HFCD) and the mouse aortic vascular smooth muscle cell (MOVAS) inflammation model induced by oxidized low-density lipoprotein (ox-LDL). Our results show that KFs significantly reduced serum lipid levels and suppressed the overproduction of inflammatory cytokines in ApoE mice. Notably, KFs also decreased the area of atherosclerotic lesions and plaque formation in the aorta of ApoE mice. Additionally, (mouse aortic tissue) and (MOVAS cells), KFs were found to inhibit the activation of NLRP3 inflammasome and simultaneously upregulate microRNA-145 (miR-145). In conclusion, our findings suggest that KFs exert their inhibitory effects on NLRP3 inflammasome through upregulating miR-145, thereby alleviating the progression of AS.

摘要

动脉粥样硬化(AS)被广泛认为是慢性炎症的结果,其中核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)炎性小体在介导这种炎症反应中起关键作用。金橘黄酮(KFs)是金橘中的主要活性成分,已显示出调节炎症的潜力,并可能有助于预防AS。在此,本研究旨在使用喂食高脂/胆固醇饮食(HFCD)的ApoE小鼠模型和由氧化低密度脂蛋白(ox-LDL)诱导的小鼠主动脉血管平滑肌细胞(MOVAS)炎症模型,探讨KFs对AS的保护作用及其潜在机制。我们的结果表明,KFs显著降低了ApoE小鼠的血脂水平,并抑制了炎性细胞因子的过量产生。值得注意的是,KFs还减少了ApoE小鼠主动脉中动脉粥样硬化病变的面积和斑块形成。此外,(小鼠主动脉组织)和(MOVAS细胞),发现KFs抑制NLRP3炎性小体的激活,并同时上调微小RNA-145(miR-145)。总之,我们的研究结果表明,KFs通过上调miR-145对NLRP3炎性小体发挥抑制作用,从而减轻AS的进展。

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