Lazic Milos, Inzaugarat Maria Eugenia, Povero Davide, Zhao Iris C, Chen Mark, Nalbandian Madlena, Miller Yury I, Cherñavsky Alejandra C, Feldstein Ariel E, Sears Dorothy D
Department of Pediatrics, University of California San Diego, La Jolla, California, United States of America.
Institute of Immunology, Genetics and Metabolism, CONICET-UBA, Buenos Aires, Argentina.
PLoS One. 2014 Sep 24;9(9):e107658. doi: 10.1371/journal.pone.0107658. eCollection 2014.
Obesity is associated with metabolic perturbations including liver and adipose tissue inflammation, insulin resistance, and type 2 diabetes. Omega-6 fatty acids (ω6) promote and omega-3 fatty acids (ω3) reduce inflammation as they can be metabolized to pro- and anti-inflammatory eicosanoids, respectively. 12/15-lipoxygenase (12/15-LO) enzymatically produces some of these metabolites and is induced by high fat (HF) diet. We investigated the effects of altering dietary ω6/ω3 ratio and 12/15-LO deficiency on HF diet-induced tissue inflammation and insulin resistance. We examined how these conditions affect circulating concentrations of oxidized metabolites of ω6 arachidonic and linoleic acids and innate and adaptive immune system activity in the liver. For 15 weeks, wild-type (WT) mice were fed either a soybean oil-enriched HF diet with high dietary ω6/ω3 ratio (11∶1, HFH), similar to Western-style diet, or a fat Kcal-matched, fish oil-enriched HF diet with a low dietary ω6/ω3 ratio of 2.7∶1 (HFL). Importantly, the total saturated, monounsaturated and polyunsaturated fat content was matched in the two HF diets, which is unlike most published fish oil studies in mice. Despite modestly increased food intake, WT mice fed HFL were protected from HFH-diet induced steatohepatitis, evidenced by decreased hepatic mRNA expression of pro-inflammatory genes and genes involved in lymphocyte homing, and reduced deposition of hepatic triglyceride. Furthermore, oxidized metabolites of ω6 arachidonic acid were decreased in the plasma of WT HFL compared to WT HFH-fed mice. 12/15-LO knockout (KO) mice were also protected from HFH-induced fatty liver and elevated mRNA markers of inflammation and lymphocyte homing. 12/15-LOKO mice were protected from HFH-induced insulin resistance but reducing dietary ω6/ω3 ratio in WT mice did not ameliorate insulin resistance or adipose tissue inflammation. In conclusion, lowering dietary ω6/ω3 ratio in HF diet significantly reduces steatohepatitis.
肥胖与包括肝脏和脂肪组织炎症、胰岛素抵抗及2型糖尿病在内的代谢紊乱有关。ω-6脂肪酸(ω6)促进炎症,而ω-3脂肪酸(ω3)减轻炎症,因为它们可分别代谢为促炎和抗炎类二十烷酸。12/15-脂氧合酶(12/15-LO)通过酶促作用产生其中一些代谢产物,并由高脂(HF)饮食诱导产生。我们研究了改变饮食中ω6/ω3比例和12/15-LO缺乏对HF饮食诱导的组织炎症和胰岛素抵抗的影响。我们研究了这些情况如何影响ω6花生四烯酸和亚油酸氧化代谢产物的循环浓度以及肝脏中固有免疫和适应性免疫系统的活性。15周内,野生型(WT)小鼠被喂食富含大豆油的高饮食ω6/ω3比例(11∶1,HFH)的HF饮食,类似于西式饮食,或脂肪千卡匹配、富含鱼油的低饮食ω6/ω3比例为2.7∶1的HF饮食(HFL)。重要的是,两种HF饮食中饱和、单不饱和和多不饱和脂肪的总含量相匹配,这与大多数已发表的小鼠鱼油研究不同。尽管食物摄入量适度增加,但喂食HFL的WT小鼠免受HFH饮食诱导的脂肪性肝炎影响,这表现为促炎基因和参与淋巴细胞归巢的基因的肝脏mRNA表达降低,以及肝脏甘油三酯沉积减少。此外,与喂食HFH的WT小鼠相比,WT HFL小鼠血浆中ω6花生四烯酸的氧化代谢产物减少。12/15-LO基因敲除(KO)小鼠也免受HFH诱导的脂肪肝以及炎症和淋巴细胞归巢的mRNA标志物升高的影响。12/15-LO KO小鼠免受HFH诱导的胰岛素抵抗,但降低WT小鼠饮食中的ω6/ω3比例并不能改善胰岛素抵抗或脂肪组织炎症。总之,降低HF饮食中的ω6/ω3比例可显著减轻脂肪性肝炎。