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白藜芦醇衍生物,反式-3,5,4'-三甲氧基二苯乙烯,可预防动脉粥样硬化斑块的形成,并减轻巨噬细胞泡沫细胞中的胆固醇蓄积。

Resveratrol Derivative, Trans-3, 5, 4'-Trimethoxystilbene, Prevents the Developing of Atherosclerotic Lesions and Attenuates Cholesterol Accumulation in Macrophage Foam Cells.

机构信息

Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, China.

Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, 510000, China.

出版信息

Mol Nutr Food Res. 2020 Mar;64(6):e1901115. doi: 10.1002/mnfr.201901115. Epub 2020 Feb 9.

Abstract

SCOPE

Recent studies have demonstrated that trans-3, 5, 4'-Trimethoxystilbene (TMS), a novel derivative of resveratrol, may suppress the foam cells formation and restrain atherosclerosis in vitro and in vivo. Herein, the molecular mechanisms underlying the protective effects of TMS against atherosclerosis are further delineated.

METHODS AND RESULTS

In the present study, the cholesterol-lowering effects of TMS in macrophage-derived foam cell by animal studies, Oil Red O staining, and lipid uptake as well as efflux analysis, are explored. Real-time PCR, western blotting analysis, luciferase reporter assay, electrophoretic mobility shift assay, and immunofluorescent staining are applied for investigating the mechanism involved in atherosclerosis prevention by TMS. Herein, it is revealed that TMS, at a dosage of 10 mg kg  day , may suppress atherosclerotic plaques within the aorta and arterial intima in apolipoprotein Edeficient mice (ApoE)-/- mice by reducing cholesterol level and macrophages content. Exposure of macrophages to TMS (10 µM) can suppress foam cells formation via regulating oxidized low density lipoprotein and cholesterol content in human macrophages through inhibiting scavenger receptors expression and activator protein-1(AP-1) activity. In addition, TMS can activate ERK/Nrf2/HO-1 signaling which increases the expression of ATP-binding cassette transporters.

CONCLUSION

In conclusion, TMS may inhibit the progress of atherosclerosis through regulating cholesterol homeostasis and inhibiting macrophage-derived foam cells formation.

摘要

范围

最近的研究表明,白藜芦醇的一种新型衍生物——反式-3,5,4'-三甲氧基二苯乙烯(TMS),可能在体外和体内抑制泡沫细胞的形成并抑制动脉粥样硬化。本文进一步阐述了 TMS 抑制动脉粥样硬化的保护作用的分子机制。

方法和结果

在本研究中,通过动物研究、油红 O 染色、脂质摄取和流出分析来探索 TMS 在巨噬细胞源性泡沫细胞中降低胆固醇的作用。实时 PCR、western blot 分析、荧光素酶报告基因检测、电泳迁移率变动分析和免疫荧光染色用于研究 TMS 预防动脉粥样硬化的机制。结果表明,TMS 在 10mg/kg/天的剂量下,可以通过降低胆固醇水平和巨噬细胞含量来抑制载脂蛋白 E 缺陷型(ApoE)-/-小鼠主动脉和动脉内膜中的动脉粥样硬化斑块。TMS(10µM)处理巨噬细胞可以通过调节人巨噬细胞中氧化型低密度脂蛋白和胆固醇含量来抑制清道夫受体表达和激活蛋白-1(AP-1)活性,从而抑制泡沫细胞形成。此外,TMS 可以激活 ERK/Nrf2/HO-1 信号通路,增加 ATP 结合盒转运蛋白的表达。

结论

总之,TMS 可能通过调节胆固醇稳态和抑制巨噬细胞源性泡沫细胞形成来抑制动脉粥样硬化的进展。

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