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Reduced Dietary Omega-6 to Omega-3 Fatty Acid Ratio and 12/15-Lipoxygenase Deficiency Are Protective against Chronic High Fat Diet-Induced Steatohepatitis

机译:降低饮食中Omega-6与Omega-3脂肪酸的比例和12 / 15-脂氧合酶缺乏症可预防慢性高脂饮食诱发的脂肪性肝炎

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摘要

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.
机译:肥胖与代谢紊乱有关,包括肝脏和脂肪组织发炎,胰岛素抵抗和2型糖尿病。 Omega-6脂肪酸(ω6)可以促进炎症,而Omega-3脂肪酸(ω3)则可以减少炎症,因为它们可以分别代谢为促炎性和抗炎性类花生酸。 12 / 15-脂氧合酶(12 / 15-LO)以酶促方式产生其中一些代谢产物,并由高脂肪(HF)饮食诱导。我们调查了饮食中ω6/ω3比值的变化和12 / 15-LO缺乏对HF饮食引起的组织炎症和胰岛素抵抗的影响。我们检查了这些条件如何影响ω6花生四烯酸和亚油酸的氧化代谢产物的循环浓度以及肝脏中先天和适应性免疫系统的活性。在15周内,向野生型(WT)小鼠饲喂高ω6/ω3比(11:1,HFH)的高大豆油HF日粮(类似于西式日粮),或饲喂与脂肪Kcal相匹配的高脂膳食。鱼油富含HF的饮食,其ω6/ω3比值低至2.7:1(HFL)。重要的是,两种HF饮食中总的饱和,单不饱和和多不饱和脂肪含量是匹配的,这与大多数已发表的小鼠鱼油研究不同。尽管进食量适度增加,但喂食HFL的WT小鼠不受HFH饮食诱导的脂肪性肝炎的保护,这由促炎基因和涉及淋巴细胞归巢的基因的肝mRNA表达降低以及肝甘油三酸酯的沉积减少证明。此外,与野生型HFH喂养的小鼠相比,野生型HFL血浆中ω6花生四烯酸的氧化代谢产物减少。还保护了12 / 15-LO基因敲除(KO)小鼠免于HFH诱导的脂肪肝以及炎症和淋巴细胞归巢的mRNA表达升高。 12 / 15-LOKO小鼠受到HFH诱导的胰岛素抵抗的保护,但是降低WT小鼠的饮食中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饮食中饮食中ω6/ω3的比例可显着减少脂肪性肝炎。

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