Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP, Av. Café s/n, 14040-903, Ribeirão Preto, SP, Brazil.
Departamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP, Av. Café s/n, 14040-903, Ribeirão Preto, SP, Brazil.
J Nutr Biochem. 2016 Feb;28:147-54. doi: 10.1016/j.jnutbio.2015.10.008. Epub 2015 Nov 1.
Clinical conditions associated with obesity can be improved by daily intake of conjugated linoleic acid (CLA) or extra virgin olive oil (EVOO). Here we investigated whether dietary supplementation with CLA and EVOO, either alone or in combination, changes body metabolism associated with mitochondrial energetics. Male C57Bl/6 mice were divided into one of four groups: CLA (1:1 cis-9, trans-11:trans-10, cis-12; 18:2 isomers), EVOO, CLA plus EVOO or control (linoleic acid). Each mouse received 3 g/kg body weight of the stated oil by gavage on alternating days for 60 days. Dietary supplementation with CLA, alone or in combination with EVOO: (a) reduced the white adipose tissue gain; (b) increased body VO2 consumption, VCO2 production and energy expenditure; (c) elevated uncoupling protein (UCP)-2 expression and UCP activity in isolated liver mitochondria. This organelle, when energized with NAD(+)-linked substrates, produced high amounts of H2O2 without inducing oxidative damage. Dietary supplementation with EVOO alone did not change any metabolic parameter, but supplementation with CLA itself promoted insulin resistance and elevated weight, lipid content and acetyl-CoA carboxylase-1 expression in liver. Interestingly, the in vivo antioxidant therapy with N-acetylcysteine abolished the CLA-induced rise of body metabolism and liver UCP expression and activity, while the in vitro antioxidant treatment with catalase mitigated the CLA-dependent UCP-2 expression in hepatocytes; these findings suggest the participation of an oxidative-dependent pathway. Therefore, this study clarifies the mechanisms by which CLA induces liver UCP expression and activity, and demonstrates for the first time the beneficial effects of combined CLA and EVOO supplementation.
共轭亚油酸(CLA)或特级初榨橄榄油(EVOO)的日常摄入可以改善与肥胖相关的临床状况。在这里,我们研究了单独或联合补充 CLA 和 EVOO 是否会改变与线粒体能量代谢相关的身体代谢。雄性 C57Bl/6 小鼠被分为四组之一:CLA(1:1 cis-9,trans-11:trans-10,cis-12;18:2 异构体)、EVOO、CLA 加 EVOO 或对照(亚油酸)。每只小鼠通过灌胃每天接受 3 g/kg 体重的指定油,持续 60 天。单独或与 EVOO 联合补充 CLA:(a)减少白色脂肪组织的增加;(b)增加全身 VO2 消耗、VCO2 产生和能量消耗;(c)升高分离的肝线粒体中的解偶联蛋白(UCP)-2 表达和 UCP 活性。这种细胞器在用 NAD(+)-连接的底物供能时会产生大量的 H2O2,而不会引起氧化损伤。单独补充 EVOO 不会改变任何代谢参数,但单独补充 CLA 本身会促进胰岛素抵抗和增加体重、肝脏脂质含量和乙酰辅酶 A 羧化酶-1 的表达。有趣的是,体内抗氧化治疗用 N-乙酰半胱氨酸消除了 CLA 引起的身体代谢和肝脏 UCP 表达和活性的增加,而体外抗氧化处理用过氧化氢酶减轻了 CLA 依赖的肝细胞中 UCP-2 的表达;这些发现表明参与了一种氧化依赖的途径。因此,本研究阐明了 CLA 诱导肝脏 UCP 表达和活性的机制,并首次证明了 CLA 和 EVOO 联合补充的有益效果。