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本文引用的文献

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Analysis of transcriptome and metabolome profiles alterations in fatty liver induced by high-fat diet in rat.高脂饮食诱导大鼠脂肪肝中转录组和代谢组谱改变的分析。
Metabolism. 2010 Apr;59(4):554-60. doi: 10.1016/j.metabol.2009.08.022. Epub 2009 Nov 14.
2
n-3 PUFA and lipotoxicity.n-3多不饱和脂肪酸与脂毒性
Biochim Biophys Acta. 2010 Mar;1801(3):362-6. doi: 10.1016/j.bbalip.2009.09.010. Epub 2009 Sep 23.
3
The state of cholesterol metabolism in the liver of patients with primary biliary cirrhosis: the role of MDR3 expression.原发性胆汁性肝硬化患者肝脏胆固醇代谢状态:MDR3 表达的作用。
Hepatol Int. 2009 Sep;3(3):490-6. doi: 10.1007/s12072-009-9137-y. Epub 2009 Jun 16.
4
A pilot study using simvastatin in the treatment of nonalcoholic steatohepatitis: A randomized placebo-controlled trial.一项使用辛伐他汀治疗非酒精性脂肪性肝炎的初步研究:一项随机安慰剂对照试验。
J Clin Gastroenterol. 2009 Nov-Dec;43(10):990-4. doi: 10.1097/MCG.0b013e31819c392e.
5
Suppression of hepatic fat accumulation by highly purified eicosapentaenoic acid prevents the progression of d-galactosamine-induced hepatitis in mice fed with a high-fat/high-sucrose diet.高纯度二十碳五烯酸抑制肝脏脂肪堆积可预防高脂/高糖饮食喂养小鼠中d-半乳糖胺诱导的肝炎进展。
Biochim Biophys Acta. 2009 Apr;1791(4):281-8. doi: 10.1016/j.bbalip.2009.01.014. Epub 2009 Jan 31.
6
Recent advances in nonalcoholic fatty liver disease.非酒精性脂肪性肝病的最新进展
Curr Opin Gastroenterol. 2009 May;25(3):230-7. doi: 10.1097/mog.0b013e3283294a18.
7
Impact of cholesterol metabolism and the LXRalpha-SREBP-1c pathway on nonalcoholic fatty liver disease.胆固醇代谢及肝X受体α-固醇调节元件结合蛋白-1c通路对非酒精性脂肪性肝病的影响
Int J Mol Med. 2009 May;23(5):603-8. doi: 10.3892/ijmm_00000170.
8
Nutritional investigation of non-obese patients with non-alcoholic fatty liver disease: the significance of dietary cholesterol.非肥胖型非酒精性脂肪性肝病患者的营养调查:膳食胆固醇的意义
Scand J Gastroenterol. 2009;44(4):471-7. doi: 10.1080/00365520802588133.
9
Efficacy of atorvastatin for the treatment of nonalcoholic steatohepatitis with dyslipidemia.阿托伐他汀治疗非酒精性脂肪性肝炎伴血脂异常的疗效。
Metabolism. 2008 Dec;57(12):1711-8. doi: 10.1016/j.metabol.2008.07.030.
10
Current and emerging therapies in nonalcoholic fatty liver disease.非酒精性脂肪性肝病的现有及新兴疗法
Semin Liver Dis. 2008 Nov;28(4):396-406. doi: 10.1055/s-0028-1091984. Epub 2008 Oct 27.

控制饮食中的胆固醇摄入对于改善非酒精性脂肪肝疾病是否足够有效?

Is the control of dietary cholesterol intake sufficiently effective to ameliorate nonalcoholic fatty liver disease?

出版信息

World J Gastroenterol. 2010 Feb 21;16(7):800-3. doi: 10.3748/wjg.v16.i7.800.

DOI:10.3748/wjg.v16.i7.800
PMID:20143458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2825326/
Abstract

In our examination of the distribution of abdominal fat, dietary intake and biochemical data in patients with nonalcoholic fatty liver disease (NAFLD), non-obese NAFLD patients without insulin resistance presented a characteristic pattern of dietary intake. Dietary cholesterol intake was superabundant in non-obese patients compared with obese patients, although total energy and carbohydrate intake was not excessive. Namely, excess cholesterol intake appears to be one of the main factors associated with NAFLD development and liver injury. Therefore, the control of dietary cholesterol intake may lead to an improvement in NAFLD, and the NPC1L1 inhibitor ezetimibe might be a promising treatment for NAFLD. We review one pathogenic aspect of lipid metabolism dysregulation in NAFLD and survey new strategies for NAFLD treatment based on the modification of cholesterol metabolism.

摘要

在研究非酒精性脂肪性肝病(NAFLD)患者的腹部脂肪分布、饮食摄入和生化数据时,我们发现非肥胖且无胰岛素抵抗的 NAFLD 患者存在一种特征性的饮食摄入模式。与肥胖患者相比,非肥胖患者的膳食胆固醇摄入量过高,尽管总能量和碳水化合物摄入量并不超标。也就是说,过量的胆固醇摄入似乎是与 NAFLD 发展和肝损伤相关的主要因素之一。因此,控制膳食胆固醇摄入可能有助于改善 NAFLD,而 NPC1L1 抑制剂依折麦布可能是治疗 NAFLD 的一种有前途的药物。我们回顾了 NAFLD 脂质代谢失调的一个发病机制方面,并根据胆固醇代谢的改变调查了 NAFLD 治疗的新策略。