首页> 美国卫生研究院文献>Scientific Reports >Substitution of linoleic acid with α-linolenic acid or long chain n-3 polyunsaturated fatty acid prevents Western diet induced nonalcoholic steatohepatitis
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Substitution of linoleic acid with α-linolenic acid or long chain n-3 polyunsaturated fatty acid prevents Western diet induced nonalcoholic steatohepatitis

机译:用α-亚麻酸或长链n-3多不饱和脂肪酸取代亚油酸可预防西方饮食引起的非酒精性脂肪性肝炎

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摘要

Imbalance in the n-6 polyunsaturated fatty acids (PUFA) and n-3 PUFA in the Western diet may increase the risk of nonalcoholic fatty liver disease (NAFLD). This study investigates the impact of substitution of linoleic acid with α-linolenic acid (ALA) or long chain (LC) n-3 PUFA and hence decreasing n-6:n-3 fatty acid ratio on high fat, high fructose (HFHF) diet induced nonalcoholic steatohepatitis (NASH). Male Sprague-Dawley rats were divided into four groups and fed control diet, HFHF diet (n-6:n-3 ratio of 200), HFHF diet with ALA (n-6:n-3 ratio of 2) or HFHF diet with LC n-3 PUFA (n-6:n-3 ratio of 5) for 24 weeks. Rats fed HFHF diet with n-6:n-3 ratio of 200 resulted in hepatic steatosis, induced glucose intolerance, insulin resistance and oxidative stress accompanied by increase in markers of inflammation, plasma lipids and aminotransferase levels. Histopathological examination of liver further confirmed the establishment of NASH. ALA and LC n-3 PUFA supplementation prevented hepatic steatosis and dyslipidemia by inhibiting lipogenesis and increasing insulin sensitivity. Furthermore, n-3 PUFA supplementation attenuated hepatic oxidative stress by restoring antioxidant status, decreased inflammation and preserved hepatic architecture. These finding suggest that decreasing n-6:n-3 ratio prevented HFHF induced NASH by attenuating oxidative stress and inflammation.
机译:西方饮食中n-6多不饱和脂肪酸(PUFA)和n-3 PUFA的不平衡可能会增加非酒精性脂肪肝疾病(NAFLD)的风险。这项研究调查了用α-亚麻酸(ALA)或长链(LC)n-3 PUFA取代亚油酸并因此降低n-6:n-3脂肪酸比率对高脂高果糖(HFHF)的影响饮食引起的非酒精性脂肪性肝炎(NASH)。将Sprague-Dawley雄性大鼠分为四组,分别喂食对照饮食,HFHF饮食(n-6:n-3比例为200),HFAL饮食和ALA(n-6:n-3比例为2)或HFHF饮食并进行饮食。 LC n-3 PUFA(n-6:n-3比例为5)持续24周。用n-6:n-3比例为200的HFHF饮食喂养的大鼠导致肝脂肪变性,诱导的葡萄糖耐量下降,胰岛素抵抗和氧化应激,并伴有炎症,血浆脂质和氨基转移酶水平的升高。肝的组织病理学检查进一步证实了NASH的建立。补充ALA和LC n-3 PUFA可通过抑制脂肪生成和增加胰岛素敏感性来预防肝脂肪变性和血脂异常。此外,n-3 PUFA补充剂通过恢复抗氧化剂状态,减轻炎症反应和保留肝结构来减轻肝氧化应激。这些发现表明,降低n-6:n-3比率可通过减轻氧化应激和炎症来预防HFHF诱导的NASH。

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