Yang Zhi-Hong, Bando Masahiro, Sakurai Toshihiro, Chen Ye, Emma-Okon Beatrice, Wilhite Bree, Fukuda Daiju, Vaisman Boris, Pryor Milton, Wakabayashi Yoshiyuki, Sampson Maureen, Yu Zu-Xi, Sakurai Akiko, Zarzour Abdalrahman, Miyahara Hiroko, Takeo Jiro, Sakaue Hiroshi, Sata Masataka, Remaley Alan T
Lipoprotein Metabolism Section, Cardio-Pulmonary Branch, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD, USA.
Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Mol Nutr Food Res. 2016 Oct;60(10):2208-2218. doi: 10.1002/mnfr.201600142. Epub 2016 Jul 12.
Fish oil-derived long-chain monounsaturated fatty acids (LCMUFA) containing chain lengths longer than 18 were previously shown to improve cardiovascular disease risk factors in mice. However, it is not known if LCMUFA also exerts anti-atherogenic effects. The main objective of the present study was to investigate the effect of LCMUFA on the development of atherosclerosis in mouse models.
LDLR-KO mice were fed Western diet supplemented with 2% (w/w) of either LCMUFA concentrate, olive oil, or not (control) for 12 wk. LCMUFA, but not olive oil, significantly suppressed the development of atherosclerotic lesions and several plasma inflammatory cytokine levels, although there were no major differences in plasma lipids between the three groups. At higher doses 5% (w/w) LCMUFA supplementation was observed to reduce pro-atherogenic plasma lipoproteins and to also reduce atherosclerosis in ApoE-KO mice fed a Western diet. RNA sequencing and subsequent qPCR analyses revealed that LCMUFA upregulated PPAR signaling pathways in liver. In cell culture studies, apoB-depleted plasma from LDLR-K mice fed LCMUFA showed greater cholesterol efflux from macrophage-like THP-1 cells and ABCA1-overexpressing BHK cells.
Our research showed for the first time that LCMUFA consumption protects against diet-induced atherosclerosis, possibly by upregulating the PPAR signaling pathway.
先前研究表明,鱼油衍生的链长超过18的长链单不饱和脂肪酸(LCMUFA)可改善小鼠心血管疾病风险因素。然而,尚不清楚LCMUFA是否也具有抗动脉粥样硬化作用。本研究的主要目的是探讨LCMUFA对小鼠模型动脉粥样硬化发展的影响。
给低密度脂蛋白受体敲除(LDLR-KO)小鼠喂食添加2%(w/w)LCMUFA浓缩物、橄榄油或不添加任何物质(对照)的西方饮食,持续12周。LCMUFA而非橄榄油显著抑制了动脉粥样硬化病变的发展以及几种血浆炎症细胞因子水平,尽管三组之间血浆脂质无显著差异。在更高剂量(5%,w/w)下,观察到补充LCMUFA可降低喂食西方饮食的载脂蛋白E敲除(ApoE-KO)小鼠的促动脉粥样硬化血浆脂蛋白,并减轻动脉粥样硬化。RNA测序及随后的定量聚合酶链反应(qPCR)分析显示,LCMUFA上调了肝脏中的过氧化物酶体增殖物激活受体(PPAR)信号通路。在细胞培养研究中,喂食LCMUFA的LDLR-K小鼠的载脂蛋白B缺失血浆显示,从巨噬细胞样THP-1细胞和过表达ATP结合盒转运体A1(ABCA1)的幼仓鼠肾(BHK)细胞中胆固醇流出增加。
我们的研究首次表明,食用LCMUFA可预防饮食诱导的动脉粥样硬化,可能是通过上调PPAR信号通路实现的。