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首页> 外文期刊>Lipids >Perilla Oil Reduces Fatty Streak Formation at Aortic Sinus via Attenuation of Plasma Lipids and Regulation of Nitric Oxide Synthase in ApoE KO Mice
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Perilla Oil Reduces Fatty Streak Formation at Aortic Sinus via Attenuation of Plasma Lipids and Regulation of Nitric Oxide Synthase in ApoE KO Mice

机译:紫苏油通过减轻血浆脂质和调节ApoE KO小鼠的一氧化氮合酶来减少主动脉窦的脂肪条纹形成

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摘要

Consumption of n-3 polyunsaturated fatty acids (PUFA) is associated with a reduced incidence of atherosclerosis. Perilla oil (PO) is a vegetable oil rich in alpha-linolenic acid (ALA), an n-3 PUFA. In this study, antiatherogenic effects and related mechanisms of PO were investigated in atherosclerotic mice. Apolipoprotein E knockout (ApoE KO) mice (male, n = 27) were fed high-cholesterol and high-fat diets containing 10 % w/w lard (LD), PO, or sunflower oil (SO) for 10 weeks. Plasma triglyceride, total cholesterol, and low-density lipoprotein cholesterol concentrations reduced in the PO and SO groups compared to the concentrations in the LD group (P < 0.05). The PO group showed reduced fatty streak lesion size at the aortic sinus (P < 0.05) compared to the sizes in the LD and SO groups. A morphometric analysis showed enhancement of endothelial nitric oxide synthase expression and reduction of inducible nitric oxide synthase expression in the PO group compared to that in the LD group (P < 0.05). Furthermore, aortic protein expression of intercellular cell adhesion molecule 1 and vascular cell adhesion molecule 1 was diminished in the PO group compared to that in the LD and SO groups (P < 0.05). These findings suggested that PO inhibited the development of aortic atherosclerosis by improving the plasma lipid profile, regulating nitric oxide synthase, and suppressing the vascular inflammatory response in the aorta of ApoE KO mice.
机译:消耗n-3多不饱和脂肪酸(PUFA)与减少动脉粥样硬化的发生有关。紫苏油(PO)是富含α-亚麻酸(ALA),n-3 PUFA的植物油。在这项研究中,对动脉粥样硬化小鼠的PO的抗动脉粥样硬化作用及其相关机制进行了研究。载脂蛋白E基因敲除(ApoE KO)小鼠(雄性,n = 27)用高胆固醇和高脂饮食喂养,这些饮食含有10%w / w猪油(LD),PO或葵花籽油(SO),历时10周。与LD组相比,PO和SO组的血浆甘油三酸酯,总胆固醇和低密度脂蛋白胆固醇浓度降低(P <0.05)。与LD组和SO组相比,PO组在主动脉窦处的脂肪条纹病变大小减小(P <0.05)。形态分析表明,与LD组相比,PO组内皮一氧化氮合酶表达增强,诱导型一氧化氮合酶表达降低(P <0.05)。此外,与LD组和SO组相比,PO组中的细胞间细胞粘附分子1和血管细胞粘附分子1的主动脉​​蛋白表达降低(P <0.05)。这些发现表明,PO通过改善血浆脂质谱,调节一氧化氮合酶并抑制ApoE KO小鼠主动脉中的血管炎性反应来抑制主动脉粥样硬化的发展。

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