• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

蛋氨酸胆碱缺乏饮食诱导的脂肪性肝炎与肝脏脂联素抵抗及肝细胞脂肪生成转化有关。

MCD-induced steatohepatitis is associated with hepatic adiponectin resistance and adipogenic transformation of hepatocytes.

作者信息

Larter Claire Z, Yeh Matthew M, Williams Jacqueline, Bell-Anderson Kim S, Farrell Geoffrey C

机构信息

ANU Medical School, Australian National University at The Canberra Hospital, Canberra, ACT, Australia.

出版信息

J Hepatol. 2008 Sep;49(3):407-16. doi: 10.1016/j.jhep.2008.03.026. Epub 2008 Apr 30.

DOI:10.1016/j.jhep.2008.03.026
PMID:18534710
Abstract

BACKGROUND/AIMS: In these studies, we tested the hypothesis that increased lipid intake would exacerbate the severity of nutritional steatohepatitis.

METHODS

C57Bl/6J mice were fed methionine-and-choline deficient (MCD) diets containing 20% (high) or 5% (low) fat by weight for 3 weeks and compared to lipid-matched controls.

RESULTS

MCD feeding increased serum ALT levels and induced hepatic steatosis, lobular inflammation and ballooning degeneration of hepatocytes, irrespective of dietary fat content. Hepatic triglyceride accumulation was similar between high and low-fat MCD-fed mice, but lipoperoxide levels were approximately 3-fold higher in the high-fat MCD-fed animals. Serum adiponectin levels increased in MCD-fed mice, although to a lesser extent in high-fat fed animals. AMPK phosphorylation was correspondingly increased in muscle of MCD-fed mice, but hepatic AMPK phosphorylation decreased, and there was little evidence of PPAR alpha activation, suggesting impaired adiponectin action in the livers of MCD-fed animals. Hepatocyte PPAR gamma mRNA levels increased in MCD-fed mice, and were associated with increased aP2 expression, indicating adipogenic transformation of hepatocytes.

CONCLUSIONS

Increased dietary lipid intake did not alter steatohepatitis severity in MCD-fed mice despite increased lipoperoxide accumulation. Instead, steatohepatitis was associated with impaired hepatic adiponectin action, and adipogenic transformation of hepatocytes in both low and high-fat MCD-fed mice.

摘要

背景/目的:在这些研究中,我们检验了以下假设,即增加脂质摄入会加重营养性脂肪性肝炎的严重程度。

方法

给C57Bl/6J小鼠喂食蛋氨酸和胆碱缺乏(MCD)饮食,其中脂肪含量按重量计为20%(高)或5%(低),持续3周,并与脂质匹配的对照组进行比较。

结果

无论饮食脂肪含量如何,MCD喂养均会增加血清ALT水平,并诱导肝脂肪变性、小叶炎症和肝细胞气球样变性。高脂和低脂MCD喂养的小鼠肝脏甘油三酯积累相似,但高脂MCD喂养的动物中脂过氧化物水平约高3倍。MCD喂养的小鼠血清脂联素水平升高,尽管在高脂喂养的动物中升高程度较小。MCD喂养的小鼠肌肉中AMPK磷酸化相应增加,但肝脏AMPK磷酸化降低,且几乎没有PPARα激活的证据,这表明MCD喂养的动物肝脏中脂联素作用受损。MCD喂养的小鼠肝细胞PPARγ mRNA水平升高,并与aP2表达增加相关,表明肝细胞发生脂肪生成转化。

结论

尽管脂过氧化物积累增加,但增加饮食脂质摄入并未改变MCD喂养小鼠的脂肪性肝炎严重程度。相反,脂肪性肝炎与肝脏脂联素作用受损以及低脂和高脂MCD喂养小鼠肝细胞的脂肪生成转化有关。

相似文献

1
MCD-induced steatohepatitis is associated with hepatic adiponectin resistance and adipogenic transformation of hepatocytes.蛋氨酸胆碱缺乏饮食诱导的脂肪性肝炎与肝脏脂联素抵抗及肝细胞脂肪生成转化有关。
J Hepatol. 2008 Sep;49(3):407-16. doi: 10.1016/j.jhep.2008.03.026. Epub 2008 Apr 30.
2
Pentoxifylline attenuates steatohepatitis induced by the methionine choline deficient diet.己酮可可碱可减轻蛋氨酸胆碱缺乏饮食诱导的脂肪性肝炎。
J Hepatol. 2004 Oct;41(4):592-8. doi: 10.1016/j.jhep.2004.06.030.
3
Activation of peroxisome proliferator-activated receptor alpha by dietary fish oil attenuates steatosis, but does not prevent experimental steatohepatitis because of hepatic lipoperoxide accumulation.膳食鱼油激活过氧化物酶体增殖物激活受体α可减轻脂肪变性,但由于肝脏脂质过氧化物积累,无法预防实验性脂肪性肝炎。
J Gastroenterol Hepatol. 2008 Feb;23(2):267-75. doi: 10.1111/j.1440-1746.2007.05157.x. Epub 2007 Sep 12.
4
Upregulation of osteopontin expression is involved in the development of nonalcoholic steatohepatitis in a dietary murine model.骨桥蛋白表达上调参与饮食诱导的小鼠非酒精性脂肪性肝炎模型的发展。
Am J Physiol Gastrointest Liver Physiol. 2004 Jul;287(1):G264-73. doi: 10.1152/ajpgi.00002.2004. Epub 2004 Mar 25.
5
Rodent nutritional model of steatohepatitis: effects of endotoxin (lipopolysaccharide) and tumor necrosis factor alpha deficiency.非酒精性脂肪性肝炎的啮齿动物营养模型:内毒素(脂多糖)和肿瘤坏死因子α缺乏的影响
J Gastroenterol Hepatol. 2006 Jan;21(1 Pt 1):174-82. doi: 10.1111/j.1440-1746.2005.04220.x.
6
Hepatic microvascular dysfunction during evolution of dietary steatohepatitis in mice.小鼠饮食性脂肪性肝炎演变过程中的肝微血管功能障碍
Hepatology. 2004 Aug;40(2):386-93. doi: 10.1002/hep.20302.
7
Quantitative trait loci analysis of mice administered the methionine-choline deficient dietary model of experimental steatohepatitis.对采用蛋氨酸-胆碱缺乏饮食模型诱导实验性脂肪性肝炎的小鼠进行数量性状基因座分析。
Liver Int. 2006 Oct;26(8):1000-5. doi: 10.1111/j.1478-3231.2006.01314.x.
8
Curcumin inhibits NF-kappaB activation and reduces the severity of experimental steatohepatitis in mice.姜黄素可抑制核因子-κB的激活,并减轻小鼠实验性脂肪性肝炎的严重程度。
J Hepatol. 2004 Dec;41(6):926-34. doi: 10.1016/j.jhep.2004.08.010.
9
NADPH oxidase is not an essential mediator of oxidative stress or liver injury in murine MCD diet-induced steatohepatitis.在小鼠蛋氨酸胆碱缺乏(MCD)饮食诱导的脂肪性肝炎中,NADPH氧化酶并非氧化应激或肝损伤的必需介质。
J Hepatol. 2007 Feb;46(2):304-13. doi: 10.1016/j.jhep.2006.08.025. Epub 2006 Nov 2.
10
Effects of iron overload in a rat nutritional model of non-alcoholic fatty liver disease.铁过载在非酒精性脂肪性肝病大鼠营养模型中的作用
Liver Int. 2006 Dec;26(10):1258-67. doi: 10.1111/j.1478-3231.2006.01329.x.

引用本文的文献

1
Advancing hepatotoxicity assessment: current advances and future directions.推进肝毒性评估:当前进展与未来方向
Toxicol Res. 2025 Apr 24;41(4):303-323. doi: 10.1007/s43188-025-00289-w. eCollection 2025 Jul.
2
Beyond obesity: lean metabolic dysfunction-associated steatohepatitis from unveiling molecular pathogenesis to therapeutic advancement.超越肥胖:从揭示分子发病机制到治疗进展的瘦素代谢功能障碍相关脂肪性肝炎
Naunyn Schmiedebergs Arch Pharmacol. 2025 May 14. doi: 10.1007/s00210-025-04257-x.
3
The deubiquitinase USP28 maintains the expression of PPARγ and its inactivation protects mice from diet-induced MASH and hepatocarcinoma.
去泛素化酶USP28维持PPARγ的表达,其失活可保护小鼠免受饮食诱导的MASH和肝癌的影响。
Mol Ther. 2025 Apr 2;33(4):1825-1841. doi: 10.1016/j.ymthe.2025.01.046. Epub 2025 Feb 3.
4
Current Treatment Regimens and Promising Molecular Therapies for Chronic Hepatobiliary Diseases.慢性肝胆疾病的当前治疗方案及有前景的分子疗法
Biomolecules. 2025 Jan 14;15(1):121. doi: 10.3390/biom15010121.
5
Non-alcoholic fatty liver disease: pathogenesis and models.非酒精性脂肪性肝病:发病机制与模型
Am J Transl Res. 2024 Feb 15;16(2):387-399. doi: 10.62347/KMSA5983. eCollection 2024.
6
Experimental Models for Studying Structural and Functional State of the Pathological Liver (Review).用于研究病理性肝脏结构和功能状态的实验模型(综述)
Sovrem Tekhnologii Med. 2023;15(4):65-82. doi: 10.17691/stm2023.15.4.06. Epub 2023 Jul 28.
7
Increased Expression of Hepatic Stearoyl-CoA Desaturase (SCD)-1 and Depletion of Eicosapentaenoic Acid (EPA) Content following Cytotoxic Cancer Therapy Are Reversed by Dietary Fish Oil.细胞毒性癌症治疗后肝酰基辅酶 A 去饱和酶 (SCD)-1 表达增加和二十碳五烯酸 (EPA) 含量减少可被饮食鱼油逆转。
Int J Mol Sci. 2023 Feb 10;24(4):3547. doi: 10.3390/ijms24043547.
8
Genetic and Diet-Induced Animal Models for Non-Alcoholic Fatty Liver Disease (NAFLD) Research.遗传和饮食诱导的非酒精性脂肪性肝病(NAFLD)动物模型研究。
Int J Mol Sci. 2022 Dec 13;23(24):15791. doi: 10.3390/ijms232415791.
9
Mouse models of nonalcoholic steatohepatitis and their application to new drug development.非酒精性脂肪性肝炎的小鼠模型及其在新药开发中的应用。
Arch Pharm Res. 2022 Nov;45(11):761-794. doi: 10.1007/s12272-022-01410-5. Epub 2022 Nov 1.
10
Mouse models of nonalcoholic fatty liver disease (NAFLD): pathomechanisms and pharmacotherapies.非酒精性脂肪性肝病(NAFLD)的小鼠模型:发病机制和药物治疗。
Int J Biol Sci. 2022 Sep 6;18(15):5681-5697. doi: 10.7150/ijbs.65044. eCollection 2022.