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Am J Physiol Gastrointest Liver Physiol 295: G197-G202, 2008. First published May 22, 2008; doi:10.1152/ajpgi.00190.2007
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LIVER AND BILIARY TRACT

The role of hepatic arterial flow on portal venous and hepatic venous wedged pressure in the isolated perfused CCl4-cirrhotic liver

Alexander Zipprich,1,2 Mauricio R. Loureiro-Silva,1,2 Irita D'Silva,2 and Roberto J. Groszmann1,2

1Digestive Disease Section, Yale University School of Medicine, New Haven, Connecticut; and 2Hepatic Hemodynamic Laboratory, Veterans Affairs Medical Center, West Haven, Connecticut

Submitted 30 April 2007 ; accepted in final form 15 May 2008

In cirrhosis, hepatic venous pressure gradient is used to measure portal venous and sinusoidal pressures, as well as drug-induced decreases of elevated pressures. The aim of this study was to investigate the influence of hepatic arterial flow (HAF) changes on portal venous perfusion (PVPP) and wedged hepatic venous pressure (WHVP). Normal and CCl4-cirrhotic rats were subjected to a bivascular liver perfusion with continuous measurements of PVPP, WHVP, and hepatic arterial perfusion pressure. Flow-pressure curves were performed with the use of different flows either through the portal vein (PVF: 20–32 ml/min) or HAF (5–15 ml/min). Increases in HAF lead to significant absolute and relative increases in PVPP (P = 0.002) and WHVP (P < 0.001). Absolute changes in HAF correlated to absolute changes in PVPP (cirrhosis: r = 0.64, P < 0.001; control: r = 0.67, P < 0.001) and WHVP (cirrhosis: r = 0.71, P < 0.001; control: r = 0.82, P < 0.001). Changes in PVPP correlated to changes in WHVP due to changes in PVF only in cirrhosis (r = 0.75, P < 0.001), whereas changes in HAF correlated in both cirrhosis (r = 0.92, P < 0.001) and control (r = 0.77, P < 0.001). In conclusion, increases and decreases in HAF lead to respective changes in PVPP and WHVP. This suggests a direct influence of HAF on PVPP and WHVP most likely due to changes in sinusoidal perfusion.

sinusoidal; CCl4-cirrhotic rats; liver perfusion



Address for reprint requests and other correspondence: R. J. Groszmann, Digestive Disease Section/111H, VA Healthcare System, 950 Campbell Ave., West Haven, CT 06516 (e-mail: roberto.groszmann{at}yale.edu)







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