Méndez-Lara Karen Alejandra, Letelier Nicole, Farré Núria, Diarte-Añazco Elena M G, Nieto-Nicolau Núria, Rodríguez-Millán Elisabeth, Santos David, Pallarès Victor, Escolà-Gil Joan Carles, Vázquez Del Olmo Tania, Lerma Enrique, Camacho Mercedes, Casaroli-Marano Ricardo P, Valledor Annabel F, Blanco-Vaca Francisco, Julve Josep
Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau i Institut d'Investigació Biomèdica de l'Hospital de la Santa Creu i Sant Pau (IIB-Sant Pau), 08041 Barcelona, Spain.
Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain.
Antioxidants (Basel). 2020 Nov 21;9(11):1162. doi: 10.3390/antiox9111162.
The potential of nicotinamide (NAM) to prevent atherosclerosis has not yet been examined. This study investigated the effect of NAM supplementation on the development of atherosclerosis in a mouse model of the disease. The development of aortic atherosclerosis was significantly reduced (NAM low dose: 45%; NAM high dose: 55%) in NAM-treated, apolipoprotein (Apo)E-deficient mice challenged with a Western diet for 4 weeks. NAM administration significantly increased (1.8-fold) the plasma concentration of proatherogenic ApoB-containing lipoproteins in NAM high-dose (HD)-treated mice compared with untreated mice. However, isolated ApoB-containing lipoproteins from NAM HD mice were less prone to oxidation than those of untreated mice. This result was consistent with the decreased (1.5-fold) concentration of oxidized low-density lipoproteins in this group. Immunohistochemical staining of aortas from NAM-treated mice showed significantly increased levels of IL-10 (NAM low-dose (LD): 1.3-fold; NAM HD: 1.2-fold), concomitant with a significant decrease in the relative expression of TNFα (NAM LD: -44%; NAM HD: -57%). An improved anti-inflammatory pattern was reproduced in macrophages cultured in the presence of NAM. Thus, dietary NAM supplementation in ApoE-deficient mice prevented the development of atherosclerosis and improved protection against ApoB-containing lipoprotein oxidation and aortic inflammation.
烟酰胺(NAM)预防动脉粥样硬化的潜力尚未得到研究。本研究调查了补充NAM对该疾病小鼠模型中动脉粥样硬化发展的影响。在用西式饮食喂养4周的载脂蛋白(Apo)E缺陷型小鼠中,经NAM处理后,主动脉粥样硬化的发展显著减少(NAM低剂量组:45%;NAM高剂量组:55%)。与未处理的小鼠相比,在高剂量(HD)NAM处理的小鼠中,NAM给药显著增加了(1.8倍)含致动脉粥样硬化ApoB的脂蛋白的血浆浓度。然而,与未处理小鼠相比,从NAM HD小鼠中分离出的含ApoB的脂蛋白更不易氧化。这一结果与该组中氧化型低密度脂蛋白浓度降低(1.5倍)一致。对经NAM处理的小鼠主动脉进行免疫组织化学染色显示,IL-10水平显著升高(NAM低剂量组(LD):1.3倍;NAM HD组:1.2倍),同时TNFα的相对表达显著降低(NAM LD组:-44%;NAM HD组:-57%)。在存在NAM的情况下培养的巨噬细胞中再现了改善的抗炎模式。因此,在ApoE缺陷型小鼠中补充膳食NAM可预防动脉粥样硬化的发展,并改善对含ApoB脂蛋白氧化和主动脉炎症的保护作用。