Literature DB >> 15372455

Expression of the hepatic endothelin system in human cirrhotic livers.

Yoshihiro Ikura1, Masahiko Ohsawa, Takahiko Naruko, Takashi Muraguchi, Michihiko Hirayama, Takehisa Suekane, Hiroko Fukushima, Yoshimi Sugama, Nobuyuki Shirai, Soichiro Kayo, Noriko Yoshimi, Shoichi Ehara, Kazuhiko Tanzawa, Makiko Ueda.   

Abstract

It is considered that endothelin-1 participates in the development of liver cirrhosis and it has been recognized that every component of the endothelin system is upregulated in cirrhotic livers. However, the expression pattern of this system, including interaction between its components, is not fully understood in human livers. In this study, the expression pattern of the endothelin system was examined. Immunohistochemical analysis for endothelin-1, endothelin receptors and endothelin-converting enzyme was performed in 16 cirrhotic and 17 normal human liver tissues. Peptides, proteins, and RNAs extracted from the livers were also investigated using quantitative assays for the components of the hepatic endothelin system. Hepatic endothelin-1 levels were significantly higher in cirrhotic livers (0.084 +/- 0.052 pg/mg wet liver) than in normal livers (0.041 +/- 0.032 pg/mg; p < 0.01), and were closely related to the severity of liver fibrosis and portal hypertension. Immunoreactivity for endothelin-1, endothelin receptors, and endothelin-converting enzyme was detected mainly in fibrous areas and in the hepatic vasculature, and was enhanced in cirrhosis. Although there was a negative correlation between the expression of receptor mRNA and the hepatic endothelin-1 level, the amounts of the mRNAs were greater in cirrhotic livers than in normal livers. However, expression of endothelin-converting enzyme in cirrhotic livers was increased at the protein level but was relatively reduced at the mRNA level. These findings suggest that the hepatic endothelin system is activated in human cirrhotic livers in association with worsening of the disease, but that the regulation of the components of this system in this disorder is complex. Copyright (c) 2004 Pathological Society of Great Britain and Ireland.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15372455     DOI: 10.1002/path.1644

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  5 in total

1.  Centrizonal arteries and microvessels in nonalcoholic steatohepatitis.

Authors:  Ryan M Gill; Patricia Belt; Laura Wilson; Nathan M Bass; Linda D Ferrell
Journal:  Am J Surg Pathol       Date:  2011-09       Impact factor: 6.394

2.  Endothelin-1 enhances fibrogenic gene expression, but does not promote DNA synthesis or apoptosis in hepatic stellate cells.

Authors:  Masahiko Koda; Michael Bauer; Anja Krebs; Eckhart G Hahn; Detlef Schuppan; Yoshikazu Murawaki
Journal:  Comp Hepatol       Date:  2006-10-24

3.  Hepatic and Plasma Endothelin-1 in Dogs with Chronic Hepatitis.

Authors:  Y Sakamoto; M Sakai; T Watari
Journal:  J Vet Intern Med       Date:  2017-03-14       Impact factor: 3.333

4.  Chronic ethanol intake modulates vascular levels of endothelin-1 receptor and enhances the pressor response to endothelin-1 in anaesthetized rats.

Authors:  C R Tirapelli; E Legros; I Brochu; J-C Honoré; V L Lanchote; S A Uyemura; A M de Oliveira; P D'Orléans-Juste
Journal:  Br J Pharmacol       Date:  2008-05-12       Impact factor: 8.739

5.  Enhanced expressions of endothelin-converting enzyme and endothelin receptors in human colonic tissues of Crohn's disease.

Authors:  Takehisa Suekane; Yoshihiro Ikura; Junko Arimoto; Masashi Nakagawa; Chizuko Kitabayashi; Takahiko Naruko; Toshio Watanabe; Yasuhiro Fujiwara; Nobuhide Oshitani; Kiyoshi Maeda; Kazuhiko Tanzawa; Kosei Hirakawa; Tetsuo Arakawa; Makiko Ueda
Journal:  J Clin Biochem Nutr       Date:  2008-03       Impact factor: 3.114

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.