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本文引用的文献

1
N-3 long-chain PUFA supplementation prevents high fat diet induced mouse liver steatosis and inflammation in relation to PPAR-α upregulation and NF-κB DNA binding abrogation.补充N-3长链多不饱和脂肪酸可预防高脂饮食诱导的小鼠肝脏脂肪变性和炎症,这与过氧化物酶体增殖物激活受体-α(PPAR-α)上调及核因子-κB(NF-κB)DNA结合消除有关。
Mol Nutr Food Res. 2014 Jun;58(6):1333-41. doi: 10.1002/mnfr.201300458. Epub 2014 Jan 16.
2
Omega-3 PUFAs improved endothelial function and arterial stiffness with a parallel antiinflammatory effect in adults with metabolic syndrome.ω-3 多不饱和脂肪酸通过平行的抗炎作用改善代谢综合征成年人的内皮功能和动脉僵硬。
Atherosclerosis. 2014 Jan;232(1):10-6. doi: 10.1016/j.atherosclerosis.2013.10.014. Epub 2013 Oct 25.
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Circulating and dietary omega-3 and omega-6 polyunsaturated fatty acids and incidence of CVD in the Multi-Ethnic Study of Atherosclerosis.循环和饮食中的欧米伽-3 和欧米伽-6 多不饱和脂肪酸与动脉粥样硬化多民族研究中的心血管疾病发生率。
J Am Heart Assoc. 2013 Dec 18;2(6):e000506. doi: 10.1161/JAHA.113.000506.
4
Pharmacology and therapeutics of omega-3 polyunsaturated fatty acids in chronic inflammatory disease.ω-3 多不饱和脂肪酸在慢性炎症性疾病中的药理学和治疗学。
Pharmacol Ther. 2014 Mar;141(3):272-82. doi: 10.1016/j.pharmthera.2013.10.010. Epub 2013 Nov 4.
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Nuclear receptor coactivators: master regulators of human health and disease.核受体共激活因子:人类健康与疾病的主要调控因子。
Annu Rev Med. 2014;65:279-92. doi: 10.1146/annurev-med-051812-145316. Epub 2013 Sep 16.
6
A high ratio of dietary n-3/n-6 polyunsaturated fatty acids improves obesity-linked inflammation and insulin resistance through suppressing activation of TLR4 in SD rats.高比例的膳食 n-3/n-6 多不饱和脂肪酸通过抑制 TLR4 的激活改善肥胖相关的炎症和胰岛素抵抗。
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7
Postnatal dietary omega-3 fatty acid supplementation rescues glucocorticoid-programmed adiposity, hypertension, and hyperlipidemia in male rat offspring raised on a high-fat diet.产后饮食中补充ω-3 脂肪酸可挽救雄性大鼠后代在高脂肪饮食下生长所导致的糖皮质激素编程性肥胖、高血压和高脂血症。
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8
Fish oil supplementation for two generations increases insulin sensitivity in rats.给两代大鼠补充鱼油可提高胰岛素敏感性。
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9
Maternal plasma polyunsaturated fatty acid status in late pregnancy is associated with offspring body composition in childhood.母亲孕晚期血浆多不饱和脂肪酸状况与儿童期后代身体成分有关。
J Clin Endocrinol Metab. 2013 Jan;98(1):299-307. doi: 10.1210/jc.2012-2482. Epub 2012 Nov 16.
10
Omega-3 fatty acids for the treatment of non-alcoholic fatty liver disease.ω-3 脂肪酸治疗非酒精性脂肪性肝病。
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亚油酸和α-亚麻酸的消耗在三代人身上产生了累积调节肝脏中与脂质代谢相关基因的表达。

Linoleic and α-linolenic fatty acid consumption over three generations exert cumulative regulation of hepatic expression of genes related to lipid metabolism.

机构信息

Department of Animal Science, Agronomy College, Federal University of Pelotas, Campus Universitário, Pelotas, RS, CEP 96010-900, Brazil,

出版信息

Genes Nutr. 2014 Jul;9(4):405. doi: 10.1007/s12263-014-0405-7. Epub 2014 May 20.

DOI:10.1007/s12263-014-0405-7
PMID:24842071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4169064/
Abstract

The essential fatty acids, omega-3 and omega-6, consumed during pregnancy can benefit maternal and offspring health. For instance, they could activate a network of genes related to the nuclear receptor peroxisome proliferator-activated receptor α (Ppara) and sterol regulatory element binding transcription factor 1 (Srebf1), which play a role in fatty acid oxidation and lipogenesis. The present study aimed to investigate the effects of diets with different omega-3/omega-6 ratio consumed over three generations on blood biochemical parameters and hepatic expression of Ppara- and Srebf1-related genes. During three consecutive generations adult Wistar rats were evaluated in the postpartum period (21 days after parturition). Regardless of prenatal dietary omega-3/omega-6 ratio, an upregulation in liver tissue was observed for Rxra, Lxra and Srebf1 and a downregulation for Fasn in all the evaluated generations. The diet with higher omega-3/omega-6 ratio decreased triacylglycerol serum levels and resulted in a constant non-esterified fatty acid level. Our results indicated that the PUFAs effect on the modulation of genes related to fatty acid oxidation and lipogenesis is cumulative through generations.

摘要

必需脂肪酸,ω-3 和 ω-6,在怀孕期间摄入可以有益于母婴健康。例如,它们可以激活与核受体过氧化物酶体增殖物激活受体-α(PPARA)和固醇调节元件结合转录因子 1(SREBF1)相关的基因网络,这些基因在脂肪酸氧化和脂肪生成中发挥作用。本研究旨在探讨在三代人期间摄入不同 ω-3/ω-6 比例的饮食对血液生化参数和肝脏中与 PPARA 和 SREBF1 相关基因表达的影响。在连续三代成年 Wistar 大鼠产后期间(分娩后 21 天)进行评估。无论产前饮食的 ω-3/ω-6 比例如何,所有评估的世代的肝组织中 Rxra、Lxra 和 Srebf1 的表达上调,而 Fasn 的表达下调。较高 ω-3/ω-6 比例的饮食降低了血清三酰甘油水平,并导致非酯化脂肪酸水平保持不变。我们的结果表明,多不饱和脂肪酸对脂肪酸氧化和脂肪生成相关基因的调节作用是通过几代人累积的。