Literature DB >> 16113492

Hemodynamic features of advanced cirrhosis due to chronic bile duct ligation.

Yasumi Katsuta1, Xue-Jun Zhang, Masaru Ohsuga, Toshio Akimoto, Hirokazu Komeichi, Shuji Shimizu, Toru Inami, Akiko Miyamoto, Katsuaki Satomura, Teruo Takano.   

Abstract

AIM: The aim of the present study was to compare the hemodynamic features of portal hypertension in rats with early cirrhosis with those of rats with advanced cirrhosis following common bile duct ligation (CBDL).
METHODS: A total of 53 male Sprague-Dawley rats were used. Hemodynamics were evaluated under conscious and unrestrained conditions 4 weeks and 8 weeks after CBDL, and 4 weeks after a sham operation. Arterial pressure and portal pressure were measured directly via catheters placed in the right femoral artery and main portal vein, respectively. The cardiac index and organ (splanchninc organs, brain, kidneys and lungs) blood flow were determined by the reference sample method using (141)Ce-labeled microspheres (15 mum in diameter). Arterial levels of endothelin-1 and nitrate/nitrite, as well as liver function variables, were also determined.
RESULTS: Portal pressure was significantly higher 8 weeks after CBDL (15.8+/-2.1, n=8) than 4 weeks after CBDL (13.9+/-2.1 mmHg, n=12, p<0.05), and the hyperdynamic circulation of the early period was attenuated (p<0.05). Although hepatic artery blood flow 4 and 8 weeks after CBDL was higher than that after sham operation (p<0.05), portal territory blood flow was not increased. There was a significant positive correlation between portal pressure and portal territory blood flow 8 weeks after CBDL (r=0.822, n=8, p=0.012). In rats with anemia 4 weeks after CBDL, the hemoglobin concentration was negatively correlated with portal territory blood flow (r=-0.597, n=12, p=0.040).
CONCLUSION: Portal pressure was higher 8 weeks after CBDL than 4 weeks after CBDL and increased with portal territory blood flow, suggesting that portal hypertension is maintained by a mechanism consistent with the forward flow theory. Anemia might exacerbate the hyperdynamic systemic circulation 4 weeks after CBDL.

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Year:  2005        PMID: 16113492     DOI: 10.1272/jnms.72.217

Source DB:  PubMed          Journal:  J Nippon Med Sch        ISSN: 1345-4676            Impact factor:   0.920


  4 in total

1.  Mesenteric and splenic contributions to portal venous CT perfusion in hepatic diffuse disease.

Authors:  Hongzan Sun; Zaiming Lu; Hongyuan Liang; Jun Xin; Yuying Gao; Qiyong Guo
Journal:  Int J Clin Exp Pathol       Date:  2014-10-15

2.  An intravital microscopic study of the hepatic microcirculation in cirrhotic mice models: relationship between fibrosis and angiogenesis.

Authors:  Eline Vanheule; Anja M Geerts; Jacques Van Huysse; Daphné Schelfhout; Marleen Praet; Hans Van Vlierberghe; Martine De Vos; Isabelle Colle
Journal:  Int J Exp Pathol       Date:  2008-12       Impact factor: 1.925

3.  Comparison of three research models of portal hypertension in mice: macroscopic, histological and portal pressure evaluation.

Authors:  Anja M Geerts; Eline Vanheule; Marleen Praet; Hans Van Vlierberghe; Martine De Vos; Isabelle Colle
Journal:  Int J Exp Pathol       Date:  2008-08       Impact factor: 1.925

4.  Experimental obstructive cholestasis: the wound-like inflammatory liver response.

Authors:  María-Angeles Aller; Jorge-Luis Arias; Jose García-Domínguez; Jose-Ignacio Arias; Manuel Durán; Jaime Arias
Journal:  Fibrogenesis Tissue Repair       Date:  2008-11-03
  4 in total

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