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有氧运动对动脉粥样硬化中 miRNA-TLR4 信号的影响。

Effect of aerobic exercise on miRNA-TLR4 signaling in atherosclerosis.

机构信息

Anesthesiology, Fujian Provincial Clinical Medical College, Fujian Provincial Hospital, Fujian Medical University, Fuzhou, China.

Anesthesiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

出版信息

Int J Sports Med. 2014 Apr;35(4):344-50. doi: 10.1055/s-0033-1349075. Epub 2013 Sep 10.

Abstract

Toll-like receptor 4 (TLR4)-tumor necrosis factor receptor 6 (TRAF6) signaling is activated in atherosclerosis (AS), inducing inflammatory mediators. Because miR-146a, a TLR4 microRNA (miRNA), can regulate TLR4 signaling during inflammatory responses, this study investigated the effects of aerobic exercise on TLR4-targeted miRNAs in AS. Apolipoprotein E-null mice fed a high-fat diet for 12 weeks were separated into 3 groups: (i) no treatment (AS), (ii) statin treatment (AD), or (iii) aerobic exercise (AE). Plaques and foam cells were observed in the untreated control and statin groups, respectively, but not in the AE group. Reduced angiotensin II (Ang II) and endothelin 1 (ET1) levels were observed in the AE group. Both treatment groups significantly altered the expression of inflammatory cytokine expression and reduced vascular TLR4 levels. Increased miR-146a and miR-126 and reduced miR-155 levels were observed in both treatment groups (all, P<0.001). miR-146a interacted with the 3' untranslated region of the TRAF6 gene, reducing its expression. Thus, aerobic exercise and statins may induce miR-146a expression, thereby reducing vascular TRAF and TLR4 signaling and vascular inflammatory injury in AS. Further analysis of this pathway may provide insight into the protective effects of aerobic exercise on vascular disease as well as new therapeutic targets.

摘要

Toll 样受体 4(TLR4)-肿瘤坏死因子受体 6(TRAF6)信号在动脉粥样硬化(AS)中被激活,诱导炎症介质。由于 miR-146a 是 TLR4 的 microRNA(miRNA),可以在炎症反应中调节 TLR4 信号,因此本研究探讨了有氧运动对 AS 中 TLR4 靶向 miRNA 的影响。12 周高脂饮食喂养的载脂蛋白 E 基因敲除小鼠被分为 3 组:(i)未治疗(AS)、(ii)他汀类药物治疗(AD)或(iii)有氧运动(AE)。未治疗对照组和他汀类药物治疗组分别观察到斑块和泡沫细胞,而 AE 组则没有。AE 组血管紧张素 II(Ang II)和内皮素 1(ET1)水平降低。两组治疗均显著改变了炎症细胞因子的表达并降低了血管 TLR4 水平。两组治疗均观察到 miR-146a 和 miR-126 增加和 miR-155 减少(均 P<0.001)。miR-146a 与 TRAF6 基因的 3'非翻译区相互作用,降低其表达。因此,有氧运动和他汀类药物可能通过诱导 miR-146a 的表达,从而减少血管 TRAF 和 TLR4 信号以及 AS 中的血管炎症损伤。对该途径的进一步分析可能为有氧运动对血管疾病的保护作用以及新的治疗靶点提供新的见解。

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