• 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

人类肝脏脂肪变性中过氧化物酶体的改变:一项定量研究。

Alterations of peroxisomes in steatosis of the human liver: a quantitative study.

作者信息

De Craemer D, Pauwels M, Van den Branden C

机构信息

Menselijke Anatomie and Embryologie, Vrije Universiteit Brussel, Belgium.

出版信息

Hepatology. 1995 Sep;22(3):744-52. doi: 10.1002/hep.1840220309.

DOI:10.1002/hep.1840220309
PMID:7657278
Abstract

We investigated the hepatocellular peroxisomes in 27 patients with steatosis of the liver by means of catalase cytochemistry, light and electron microscopic study, and morphometry. Seven normal human livers were used as controls. In our patients, fatty liver was mainly associated with alcohol abuse or obesity. Indications for a slight decrease in catalase activity and for a proliferation were found in visual evaluation of the peroxisomes. Morphometric analysis showed a significant decrease in mean peroxisomal diameter (to 87%) and a simultaneous significant elevation to numerical density of the peroxisomes (to 188%); this resulted in a normal volume density and a significant increase to (133%) in surface density. However, individual differences were found. No differences in peroxisomal characteristics were found between fatty livers of different causes. A significant inverse linear correlation between mean peroxisomal diameter and numerical density was found in patients with fatty livers. Because a similar correlation was also found when control data were added to the fatty liver data, we hypothesize that the peroxisomal compartment in human fatty livers is adapted in such a way to permit the same metabolic efficiency as in control livers.

摘要

我们通过过氧化氢酶细胞化学、光镜和电镜研究以及形态测量法,对27例肝脂肪变性患者的肝细胞过氧化物酶体进行了研究。选取7例正常人类肝脏作为对照。在我们的患者中,脂肪肝主要与酒精滥用或肥胖有关。在对过氧化物酶体的视觉评估中,发现过氧化氢酶活性略有下降和过氧化物酶体增殖的迹象。形态测量分析显示,过氧化物酶体平均直径显著减小(降至87%),而过氧化物酶体的数量密度同时显著升高(升至188%);这导致了正常的体积密度,表面密度显著增加(升至133%)。然而,发现了个体差异。不同病因的脂肪肝之间过氧化物酶体特征未发现差异。在脂肪肝患者中,过氧化物酶体平均直径与数量密度之间存在显著的负线性相关性。由于将对照数据添加到脂肪肝数据中时也发现了类似的相关性,我们推测人类脂肪肝中的过氧化物酶体区室以这种方式进行了适应性调整,以实现与对照肝脏相同的代谢效率。

相似文献

1
Alterations of peroxisomes in steatosis of the human liver: a quantitative study.人类肝脏脂肪变性中过氧化物酶体的改变:一项定量研究。
Hepatology. 1995 Sep;22(3):744-52. doi: 10.1002/hep.1840220309.
2
Alterations of hepatocellular peroxisomes in patients with cancer. Catalase cytochemistry and morphometry.癌症患者肝细胞过氧化物酶体的改变。过氧化氢酶细胞化学与形态测定法。
Cancer. 1993 Jun 15;71(12):3851-8. doi: 10.1002/1097-0142(19930615)71:12<3851::aid-cncr2820711210>3.0.co;2-l.
3
Morphometric characteristics of human hepatocellular peroxisomes in alcoholic liver disease.
Alcohol Clin Exp Res. 1996 Aug;20(5):908-13. doi: 10.1111/j.1530-0277.1996.tb05270.x.
4
Peroxisomes in cirrhosis of the human liver: a cytochemical, ultrastructural and quantitative study.人类肝硬化中的过氧化物酶体:细胞化学、超微结构及定量研究
Hepatology. 1993 Mar;17(3):404-10. doi: 10.1016/0270-9139(93)90051-n.
5
Peroxisomes in liver, kidney and duodenum of nude mice bearing xenografts of human pancreatic adenocarcinomas.携带人胰腺腺癌异种移植瘤的裸鼠肝脏、肾脏和十二指肠中的过氧化物酶体。
Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;64(1):7-12. doi: 10.1007/BF02915090.
6
A peculiar distribution of peroxisomes in a patient with nodular regenerative hyperplasia of the liver.一名患有肝脏结节性再生性增生患者的过氧化物酶体的特殊分布。
J Hepatol. 1994 Mar;20(3):394-7. doi: 10.1016/s0168-8278(94)80014-6.
7
Secondary alterations of human hepatocellular peroxisomes.人类肝细胞过氧化物酶体的继发性改变。
J Inherit Metab Dis. 1995;18 Suppl 1:181-213. doi: 10.1007/BF00711439.
8
Hepatocellular peroxisomes in human alcoholic and drug-induced hepatitis: a quantitative study.
Hepatology. 1991 Nov;14(5):811-7. doi: 10.1002/hep.1840140512.
9
Application of automatic image analysis for morphometric studies of peroxisomes stained cytochemically for catalase. II. Light-microscopic application.自动图像分析在过氧化氢酶细胞化学染色的过氧化物酶体形态计量学研究中的应用。II. 光学显微镜应用。
Cell Tissue Res. 1987 Jan;247(1):179-85. doi: 10.1007/BF00216560.
10
Morphometric cytochemistry of diminution of catalase-containing peroxisomes in copper-loaded liver.铜负荷肝脏中含过氧化氢酶过氧化物酶体减少的形态计量细胞化学
Histochem J. 1989 Feb;21(2):63-71. doi: 10.1007/BF01005981.

引用本文的文献

1
Induction of Peroxisomal β-Oxidation as a Critical Mechanism for Ethanol-Induced Hepatic Triglyceride Accumulation.过氧化物酶体β-氧化的诱导作为乙醇诱导肝甘油三酯积累的关键机制。
FASEB Bioadv. 2025 May 2;7(6):e70013. doi: 10.1096/fba.2024-00211. eCollection 2025 Jun.
2
Rising Influence of Nanotechnology in Addressing Oxidative Stress-Related Liver Disorders.纳米技术在应对氧化应激相关肝脏疾病中的影响力日益增强。
Antioxidants (Basel). 2023 Jul 9;12(7):1405. doi: 10.3390/antiox12071405.
3
Green Tea and Epigallocatechin Gallate (EGCG) for the Management of Nonalcoholic Fatty Liver Diseases (NAFLD): Insights into the Role of Oxidative Stress and Antioxidant Mechanism.
绿茶和表没食子儿茶素没食子酸酯(EGCG)用于非酒精性脂肪性肝病(NAFLD)的管理:对氧化应激和抗氧化机制作用的见解
Antioxidants (Basel). 2021 Jul 5;10(7):1076. doi: 10.3390/antiox10071076.
4
The Alterations of Mitochondrial Function during NAFLD Progression-An Independent Effect of Mitochondrial ROS Production.非酒精性脂肪性肝病(NAFLD)进展过程中线粒体功能的改变-线粒体 ROS 产生的独立影响。
Int J Mol Sci. 2021 Jun 25;22(13):6848. doi: 10.3390/ijms22136848.
5
Genome-Wide Detection of Key Genes and Epigenetic Markers for Chicken Fatty Liver.鸡脂肪肝关键基因和表观遗传标记的全基因组检测。
Int J Mol Sci. 2020 Mar 5;21(5):1800. doi: 10.3390/ijms21051800.
6
The proteome of human liver peroxisomes: identification of five new peroxisomal constituents by a label-free quantitative proteomics survey.人类肝脏过氧化物酶体的蛋白质组学:通过无标记定量蛋白质组学调查鉴定五个新的过氧化物酶体成分。
PLoS One. 2013;8(2):e57395. doi: 10.1371/journal.pone.0057395. Epub 2013 Feb 27.
7
Metabolic liver disease of obesity and role of adipose tissue in the pathogenesis of nonalcoholic fatty liver disease.肥胖的代谢性肝病及脂肪组织在非酒精性脂肪性肝病发病机制中的作用。
World J Gastroenterol. 2007 Jul 14;13(26):3540-53. doi: 10.3748/wjg.v13.i26.3540.
8
A growing burden: the pathogenesis, investigation and management of non-alcoholic fatty liver disease.日益加重的负担:非酒精性脂肪性肝病的发病机制、研究与管理
J Clin Pathol. 2007 Dec;60(12):1384-91. doi: 10.1136/jcp.2006.044891. Epub 2007 May 4.
9
Quantitative assessment of fibrosis and steatosis in liver biopsies from patients with chronic hepatitis C.慢性丙型肝炎患者肝活检中纤维化和脂肪变性的定量评估。
J Clin Pathol. 2001 Jun;54(6):461-5. doi: 10.1136/jcp.54.6.461.
10
Secondary alterations of human hepatocellular peroxisomes.人类肝细胞过氧化物酶体的继发性改变。
J Inherit Metab Dis. 1995;18 Suppl 1:181-213. doi: 10.1007/BF00711439.