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间断禁食对非酒精性脂肪肝脂质过氧化作用的影响 被引量:1

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摘要 目的研究间断禁食对非酒精性脂肪肝脂质过氧化是否有影响。方法选择65名非酒精性脂肪肝患者,分为实验组和对照组。实验组要求间断禁食,对照组进食时间不受限制。测定实验前后血清胆固醇、甘油三酯、高密度脂蛋白、低密度脂蛋白、血清丙二醛、超氧化物歧化酶、谷胱甘肽过氧化物酶水平。结果间断禁食后血清胆固醇、甘油三酯、低密度脂蛋白、血清丙二醛明显降低,高密度脂蛋白、超氧化物歧化酶、谷胱甘肽过氧化物酶水平明显升高,与对照组比较差异有统计学意义(p<0.05)。结论间断禁食具有调血脂和抗脂质过氧化作用,明显改善非酒精性脂肪肝的代谢紊乱。 Objective:To investigate whether intermittent fasting can affect lipid peroxidation in nonalcoholic fatty liver disease.Methods:Methods 65 patients with nonalcoholic fatty liver disease were divided into two groups: experimental group and control group. The experimental group required intermittent fasting, and the control group was free of food restriction. The levels of serum cholesterol, triglyceride, high-density lipoprotein, low-density lipoprotein, serum malondialdehyde, superoxide dismutase and glutathione peroxidase(GSH PX) were measured before and after the experiment.Results:After intermittent fasting,Cholesterol, triglyceride, low-density lipoprotein, serum malondialdehyde decreased significantly. The levels of high-density lipoprotein, superoxide dismutase and glutathione peroxidase increased significantly, the difference was statistically significant compared with the control group(P < 0.05).Conclusion:Intermittent fasting can adjust the blood lipid and lipid peroxidation、anti lipid peroxidation and improve the metabolic disorder of nonalcoholic fatty liver disease.
出处 《中国妇幼健康研究》 2017年第S3期327-328,共2页 Chinese Journal of Woman and Child Health Research
关键词 间断禁食 非酒精性脂肪肝 脂质过氧化 intermittent fasting nonalcoholic fatty liver disease lipid peroxidation
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  • 1南月敏,乔梁,于君,吴文娟,姚希贤.Fas及其配体诱导非酒精性脂肪性肝炎肝细胞凋亡[J].中华消化杂志,2006,26(12):841-842. 被引量:12
  • 2范建高.正确认识脂肪肝的危害[J].中华全科医师杂志,2007,6(4):199-200. 被引量:25
  • 3王春华,陈东风.线粒体膜通透性转换孔在非酒精性脂肪肝细胞凋亡中的作用[J].重庆医学,2007,36(8):714-715. 被引量:7
  • 4Misra A, Jaiswal A, Shakti D, et al. Novel phenotypic markers and screening score for the metabolic syndrome in adult Asian Indians [ J ]. Diabetes Rese Clini Pract ,2008,79 (2) : el-eS.
  • 5Day CP. Non-alcoholic fatty liver disease : a massive problem [ J ]. Clin Med,2011,11 (2) :176-178.
  • 6Marchesini G, Brizi M, Bianchi G, et al. Nonalcoholic fatter liver disease : a feature of the metabolic syndrome [ J ]. Diabetes, 2001, 50(8) :1844-1850.
  • 7Sanyal AJ, Campbell-Sargent C, Mirshabi F, et al. Nonalcoholic steatohepatitis: assoeiatiort of insulin resistance and mitoehondrla abnormalities [ J ]. Gastroenterology, 2001,120 ( 5 ) : 1183-1192.
  • 8Liu YF, Hemchkovitz A, Boura-Halfon S, et al. Serine phosphoryla- tion proximal to its phosphotyrosine binding domain inhibits insulin receptor substrate 1 function and promotes insulin resistance[ J ]. Mol Cell Biol,2004,24(21 ):9668-9681.
  • 9Shimomura I, Bashmakov Y, Horton JD. Increased levels of nuclear SREBP-1 c associated with fatty livem in two mouse models of dia- betes mellitus [ J]. J Biol Chem, 1999,274 (42) :30028-30032.
  • 10Sanyal AJ. Mechanisms of Disease: pathogenesis of nonalcobolic fatty liver disease [ J ]. Nat Clin Pract Gastroenteml Hepatol,2005, 2(1) :46-53.

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