Institute of Animal Nutrition and Nutrition Physiology, Justus-Liebig-Universität Gießen, Heinrich-Buff-Ring 26-32, 35392 Gießen, Germany.
Br J Nutr. 2011 Jan;105(2):190-9. doi: 10.1017/S0007114510003478. Epub 2010 Sep 21.
Activators of PPARα have been demonstrated to inhibit atherosclerosis development due to lipid lowering in plasma and direct protective effects on the vasculature. Because dietary oxidised fats (OF) have strong PPARα-activating and lipid-lowering properties, we hypothesised that dietary OF has also an inhibitory influence on atherosclerosis development. To verify our hypothesis, we investigated the effect of feeding diets containing an OF (a 92 : 8 mixture of heated (170°C, 48 h) hydrogenated palm fat and fresh sunflower oil) compared with a fresh fat (fresh hydrogenated palm fat) on the development of atherosclerotic lesions in LDL receptor-deficient (LDLR- / - ) mice. We observed that a dietary OF caused a strong up-regulation of PPARα-regulated genes in the liver and a marked reduction in plasma concentrations of cholesterol and TAG (P < 0·05). Cross-sectional lesion area and the lipids and collagen levels in the aortic root were approximately 40-50 % lower in mice fed diets containing OF than in those fed diets containing fresh fat (P < 0·05). Immunohistochemical analysis of aortic root sections revealed an about 8-fold increased expression of PPARα and a markedly reduced expression of the proinflammatory vascular cell adhesion molecule-1 and smooth muscle cell (SMC)-specific marker α-actin in LDLR- / - mice fed OF (P < 0·05). We postulate that OF exert anti-atherogenic effects by activation of PPARα both in the liver, which contributes to lipid lowering in plasma, and in the vasculature, which inhibits pro-atherogenic events such as monocyte recruitment and SMC proliferation and migration.
过氧化物酶体增殖物激活受体 α(PPARα)的激活物已被证明可以通过降低血浆中的脂质水平和对血管的直接保护作用来抑制动脉粥样硬化的发展。由于饮食中的氧化脂肪(OF)具有很强的 PPARα 激活和降血脂作用,我们假设饮食 OF 也对动脉粥样硬化的发展具有抑制作用。为了验证我们的假设,我们研究了含有 OF(加热(170°C,48 h)氢化棕榈油和新鲜葵花籽油的 92:8 混合物)的饮食与新鲜脂肪(新鲜氢化棕榈油)相比对 LDL 受体缺陷(LDLR-/-)小鼠动脉粥样硬化病变发展的影响。我们观察到,饮食 OF 可强烈上调肝脏中 PPARα 调节的基因,并显著降低血浆胆固醇和 TAG 浓度(P < 0·05)。含有 OF 的饮食组小鼠的横截面积病变和主动脉根部的脂质和胶原水平比含有新鲜脂肪的饮食组小鼠低约 40-50%(P < 0·05)。主动脉根部切片的免疫组织化学分析显示,在喂食 OF 的 LDLR-/-小鼠中,PPARα 的表达增加了约 8 倍,促炎血管细胞粘附分子-1 和平滑肌细胞(SMC)特异性标志物 α-肌动蛋白的表达明显降低(P < 0·05)。我们推测,OF 通过激活 PPARα 在肝脏中发挥抗动脉粥样硬化作用,这有助于降低血浆中的脂质,同时在血管中抑制单核细胞募集和 SMC 增殖和迁移等促动脉粥样硬化事件。