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相似文献

1
The biochemical pathology of liver cell necrosis.肝细胞坏死的生化病理学
Am J Pathol. 1975 Oct;81(1):237-50.
2
D-galactosamine and acute liver cell injury.D-半乳糖胺与急性肝细胞损伤
Fed Proc. 1973 Apr;32(4):1516-26.
3
Early, reversible plasma membrane injury in galactosamine-induced liver cell death.半乳糖胺诱导的肝细胞死亡中早期可逆的质膜损伤
Am J Pathol. 1975 Jun;79(3):579-96.
4
Prevention of galactosamine-induced liver cell necrosis by uridine.尿苷对氨基半乳糖诱导的肝细胞坏死的预防作用
Am J Pathol. 1973 Jul;72(1):53-62.
5
[Animal disease models--injury, death and various changes of liver cells].[动物疾病模型——肝细胞的损伤、死亡及各种变化]
Nihon Rinsho. 1985 Jun;43(6):1239-50.
6
Metal-induced hepatotoxicity.金属诱导的肝毒性。
Semin Liver Dis. 1996 Feb;16(1):3-12. doi: 10.1055/s-2007-1007214.
7
Galactosamine induced liver injury.半乳糖胺诱导的肝损伤。
Prog Liver Dis. 1972;4:183-99.
8
Glycine and uridine prevent D-galactosamine hepatotoxicity in the rat: role of Kupffer cells.甘氨酸和尿苷预防大鼠D-半乳糖胺肝毒性:库普弗细胞的作用
Hepatology. 1999 Mar;29(3):737-45. doi: 10.1002/hep.510290335.
9
Cystamine modulation of galactosamine-induced hepatotoxicity.半胱胺对氨基半乳糖诱导的肝毒性的调节作用。
Toxicol Appl Pharmacol. 1984 May;73(3):551-8. doi: 10.1016/0041-008x(84)90107-8.
10
Synergistic action of hepatocyte membrane defect and activated complement system in liver cell death--an experimental approach to fulminant hepatic failure.肝细胞膜缺陷与活化补体系统在肝细胞死亡中的协同作用——暴发性肝衰竭的实验研究方法
Acta Hepatogastroenterol (Stuttg). 1978 Apr;25(2):105-10.

引用本文的文献

1
Metabolic Hijacking of Hexose Metabolism to Ascorbate Synthesis Is the Unifying Biochemical Basis of Murine Liver Fibrosis.己糖代谢向抗坏血酸合成的代谢劫持是小鼠肝纤维化的统一生化基础。
Cells. 2023 Feb 2;12(3):485. doi: 10.3390/cells12030485.
2
The Interplay of Reactive Oxygen Species, Hypoxia, Inflammation, and Sirtuins in Cancer Initiation and Progression.活性氧、缺氧、炎症和沉默调节蛋白在癌症发生和发展中的相互作用
Oxid Med Cell Longev. 2016;2016:3907147. doi: 10.1155/2016/3907147. Epub 2015 Dec 20.
3
Hepatotoxin-induced changes in the adult murine liver promote MYC-induced tumorigenesis.肝毒素诱导的成年小鼠肝脏变化促进MYC诱导的肿瘤发生。
PLoS One. 2008 Jun 18;3(6):e2493. doi: 10.1371/journal.pone.0002493.
4
Expression of TNF-alpha and immunohistochemical distribution of hepatic macrophage surface markers in carbon tetrachloride-induced chronic liver injury in rats.四氯化碳诱导的大鼠慢性肝损伤中TNF-α的表达及肝巨噬细胞表面标志物的免疫组化分布
Histochem J. 1999 Oct;31(10):677-85. doi: 10.1023/a:1003851821487.
5
The nature and significance of liver cell vacuolation following hepatocellular injury--an analysis based on observations on rats rendered tolerant to hepatotoxic damage.肝细胞损伤后肝细胞空泡化的性质及意义——基于对耐受肝毒性损伤大鼠的观察分析
Virchows Arch. 1996 Aug;428(6):353-65. doi: 10.1007/BF00202202.
6
[The electrolyte composition of liver preservation solutions for hepatocytes in a model of in vitro preservation and reoxygenation].[体外保存与复氧模型中用于肝细胞的肝脏保存液的电解质组成]
Langenbecks Arch Chir. 1994;379(4):210-7. doi: 10.1007/BF00186360.
7
Membrane characteristics of adult rat liver parenchymal cells in primary monolayer culture.原代单层培养的成年大鼠肝实质细胞的膜特性
In Vitro. 1980 Oct;16(10):833-46. doi: 10.1007/BF02619420.
8
Galactosamine-induced cell death in primary cultures of rat hepatocytes.半乳糖胺诱导大鼠原代肝细胞培养物中的细胞死亡。
Am J Pathol. 1980 Jul;100(1):25-38.
9
Calcium amelioration of cadmium-induced cytotoxicity in cultured rat hepatocytes.钙对镉诱导的培养大鼠肝细胞毒性的改善作用
In Vitro. 1984 Oct;20(10):771-9. doi: 10.1007/BF02618293.
10
The sequential analysis of liver cell necrosis: inhibition of diethylnitrosamine- and dimethylnitrosamine-induced acute liver cell death by posttreatment with diethyldithiocarbamate.肝细胞坏死的序贯分析:用二乙基二硫代氨基甲酸盐进行后处理对二乙基亚硝胺和二甲基亚硝胺诱导的急性肝细胞死亡的抑制作用
Am J Pathol. 1980 Apr;99(1):159-74.

本文引用的文献

1
The metabolism of d-galactosamine and N-acetyl-d-galactosamine in rat liver.半乳糖胺和 N-乙酰半乳糖胺在大鼠肝内的代谢。
Biochem J. 1968 May;107(5):637-44. doi: 10.1042/bj1070637.
2
The development in the rat of fatty livers associated with reduced plasma-lipoprotein synthesis.大鼠脂肪肝的发展与血浆脂蛋白合成减少有关。
Biochim Biophys Acta. 1962 Jul 30;62:163-5. doi: 10.1016/0006-3002(62)90502-4.
3
Blood enzymes in liver injury following dimethylnitrosamine poisoning.二甲基亚硝胺中毒后肝损伤中的血液酶
J Pathol Bacteriol. 1962 Apr;83:483-90.
4
Effect of carbon tetrachloride on release of free fatty acids by rat adipose tissue.四氯化碳对大鼠脂肪组织释放游离脂肪酸的影响。
Proc Soc Exp Biol Med. 1960 Feb;103:398-400. doi: 10.3181/00379727-103-25535.
5
Mechanism of action of carbon tetrachloride.四氯化碳的作用机制。
Fed Proc. 1959 Dec;18:1013-20.
6
CORRESPONDENCE BETWEEN RIBOSOME AGGREGATION PATTERNS IN RAT LIVER HOMOGENATES AND IN ELECTRON MICROGRAPHS FOLLOWING ADMINISTRATION OF ETHIONINE.乙硫氨酸给药后大鼠肝脏匀浆中核糖体聚集模式与电子显微镜图像之间的对应关系。
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7
RAT LIVER AND PLASMA LIPIDS AFTER CARBON TETRACHLORIDE ADMINISTRATION.四氯化碳给药后的大鼠肝脏和血浆脂质
J Lipid Res. 1965 Apr;6:278-86.
8
ACTINOMYCIN D. EFFECTS ON NUCLEIC ACID AND PROTEIN METABOLISM IN INTACT AND REGENERATING LIVER OF RATS.放线菌素D。对大鼠完整肝脏和再生肝脏中核酸与蛋白质代谢的影响。
Cancer Res. 1965 Apr;25:307-17.
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LIVER PARENCHYMAL CELL INJURY. II. CYTOCHEMICAL EVENTS CONCERNED WITH MITOCHONDRIAL DYSFUNCTION FOLLOWING POISONING WITH CARBON TETRACHLORIDE.肝实质细胞损伤。II. 四氯化碳中毒后与线粒体功能障碍相关的细胞化学事件。
Lab Invest. 1964 Nov;13:1457-70.
10
EFFECT OF CARBON TETRACHLORIDE INGESTION ON LIVER AND PLASMA TRIGLYCERIDE TURNOVER RATES.四氯化碳摄入对肝脏和血浆甘油三酯周转率的影响。
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肝细胞坏死的生化病理学

The biochemical pathology of liver cell necrosis.

作者信息

Farber J L, El-Mofty S K

出版信息

Am J Pathol. 1975 Oct;81(1):237-50.

PMID:1180333
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2032295/
Abstract

Cell death and necrosis are important reactions of liver cells to injury that play a role in a wide variety of human liver diseases. A review is given of the important facets known about the biochemical basis of toxic liver cell death. Liver cells can withstand a great many specific biochemical and morphologic changes without loss of viability. Disturbances in RNA and protein synthesis, mitochondrial function, or release of lysosomal enzymes do not play a primary causative role in cell death. Many previous studies have tended to implicate the plasma membrane and its presumed role in maintaining the proper Ca2+ balance as the primary site of the development of irreversible hepatocyte damage. These studies have generally faced a major difficulty in determining if the observed changes are the cause or an effect of cell death. Galactosamine-induced liver cell injury seems to offer a potentially analyzable model for the experimental analysis of liver cell necrosis. Our studies on the role of plasma membrane injury and associated increases in total cellular calcium are reviewed, and a tentative working hypothesis for the pathogenesis of galactosamine-induced liver cell necrosis is presented.

摘要

细胞死亡和坏死是肝细胞对损伤的重要反应,在多种人类肝脏疾病中起作用。本文综述了关于毒性肝细胞死亡生化基础的已知重要方面。肝细胞能够承受许多特定的生化和形态学变化而不丧失活力。RNA和蛋白质合成、线粒体功能或溶酶体酶释放的紊乱在细胞死亡中并不起主要的致病作用。许多先前的研究倾向于认为质膜及其在维持适当钙平衡中的假定作用是不可逆肝细胞损伤发生的主要部位。这些研究在确定观察到的变化是细胞死亡的原因还是结果时通常面临一个主要困难。半乳糖胺诱导的肝细胞损伤似乎为肝细胞坏死的实验分析提供了一个潜在可分析的模型。我们对质膜损伤作用及细胞总钙含量相关增加的研究进行了综述,并提出了半乳糖胺诱导肝细胞坏死发病机制的初步工作假说。