Role of hemostatic factors in hepatic injury and disease: animal models de-liver

被引:37
作者
Kopec, A. K. [1 ,3 ]
Joshi, N. [2 ,3 ]
Luyendyk, J. P. [1 ,2 ,3 ]
机构
[1] Michigan State Univ, Dept Pathobiol & Diagnost Invest, 1129 Farm Lane,253 Food Safety & Toxicol Bldg, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Pharmacol & Toxicol, E Lansing, MI 48824 USA
[3] Michigan State Univ, Inst Integrat Toxicol, E Lansing, MI 48824 USA
基金
美国国家卫生研究院;
关键词
acute liver failure; animal models; coagulation; hemostasis; liver; BILE-DUCT LIGATION; CARBON-TETRACHLORIDE; TISSUE FACTOR; UNITED-STATES; INTRAVASCULAR COAGULATION; ANTIPLATELET THERAPY; PROTHROMBIN TIME; BILIARY FIBROSIS; MURINE MODEL; MOUSE MODEL;
D O I
10.1111/jth.13327
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic liver damage is associated with unique changes in the hemostatic system. Patients with liver disease often show a precariously rebalanced hemostatic system, which is easily tipped towards bleeding or thrombotic complications by otherwise benign stimuli. In addition, some clinical studies have shown that hemostatic system components contribute to the progression of liver disease. There is a strong basic science foundation for clinical studies with this particular focus. Chronic and acute liver disease can be modeled in rodents and large animals with a variety of approaches, which span chronic exposure to toxic xenobiotics, diet-induced obesity, and surgical intervention. These experimental approaches have now provided strong evidence that, in addition to perturbations in hemostasis caused by liver disease, elements of the hemostatic system have powerful effects on the progression of experimental liver toxicity and disease. In this review, we cover the basis of the animal models that are most often utilized to assess the impact of the hemostatic system on liver disease, and highlight the role that coagulation proteases and their targets play in experimental liver toxicity and disease, emphasizing key similarities and differences between models. The need to characterize hemostatic changes in existing animal models and to develop novel animal models recapitulating the coagulopathy of chronic liver disease is highlighted. Finally, we emphasize the continued need to translate knowledge derived from highly applicable animal models to improve our understanding of the reciprocal interaction between liver disease and the hemostatic system in patients.
引用
收藏
页码:1337 / 1349
页数:13
相关论文
共 100 条
[1]   A study of unfractionated and low molecular weight heparins in a model of cholestatic liver injury in the rat [J].
Abdel-Salam, OME ;
Baiuomy, AR ;
Ameen, A ;
Hassan, NS .
PHARMACOLOGICAL RESEARCH, 2005, 51 (01) :59-67
[2]   Low molecular weight heparin prevents hepatic fibrogenesis caused by carbon tetrachloride in the rat [J].
Abe, Wataru ;
Ikejima, Kenichi ;
Lang, Tie ;
Okumura, Kyoko ;
Enomoto, Nobuyuki ;
Kitamura, Tsuneo ;
Takei, Yoshiyuki ;
Sato, Nobuhiro .
JOURNAL OF HEPATOLOGY, 2007, 46 (02) :286-294
[3]   Bile Acids Induce Inflammatory Genes in Hepatocytes A Novel Mechanism of Inflammation during Obstructive Cholestasis [J].
Allen, Katryn ;
Jaeschke, Hartmut ;
Copple, Bryan L. .
AMERICAN JOURNAL OF PATHOLOGY, 2011, 178 (01) :175-186
[4]   Coagulation status modulates murine hepatic fibrogenesis: implications for the development of novel therapies [J].
Anstee, Q. M. ;
Goldin, R. D. ;
Wright, M. ;
Martinelli, A. ;
Cox, R. ;
Thursz, M. R. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2008, 6 (08) :1336-1343
[5]   The role of hypercoagulability in liver fibrogenesis [J].
Anstee, Quentin M. ;
Dhar, Ameet ;
Thursz, Mark R. .
CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 2011, 35 (8-9) :526-533
[6]   Tissue factor-protease-activated receptor 2 signaling promotes diet-induced obesity and adipose inflammation [J].
Badeanlou, Leylla ;
Furlan-Freguia, Christian ;
Yang, Guang ;
Ruf, Wolfram ;
Samad, Fahumiya .
NATURE MEDICINE, 2011, 17 (11) :1490-U200
[7]   Serum Proteomics and Biomarker Discovery Across the Spectrum of Nonalcoholic Fatty Liver Disease [J].
Bell, Lauren N. ;
Theodorakis, Janice L. ;
Vuppalanchi, Raj ;
Saxena, Romil ;
Bemis, Kerry G. ;
Wang, Mu ;
Chalasani, Naga .
HEPATOLOGY, 2010, 51 (01) :111-120
[8]   Critical role of plasminogen activator inhibitor-1 in cholestatic liver injury and fibrosis [J].
Bergheim, I ;
Guo, LP ;
Davis, MA ;
Duveau, I ;
Arteel, GE .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 316 (02) :592-600
[9]   Pro-Regenerative Signaling after Acetaminophen-Induced Acute Liver Injury in Mice Identified Using a Novel Incremental Dose Model [J].
Bhushan, Bharat ;
Walesky, Chad ;
Manley, Michael ;
Gallagher, Tara ;
Borude, Prachi ;
Edwards, Genea ;
Monga, Satdarshan P. S. ;
Apte, Udayan .
AMERICAN JOURNAL OF PATHOLOGY, 2014, 184 (11) :3013-3025
[10]   ORAL TOXICITY OF CARBON-TETRACHLORIDE - ACUTE, SUBACUTE, AND SUBCHRONIC STUDIES IN RATS [J].
BRUCKNER, JV ;
MACKENZIE, WF ;
MURALIDHARA, S ;
LUTHRA, R ;
KYLE, GM ;
ACOSTA, D .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1986, 6 (01) :16-34