|
|
||||||||
AJP - Gastrointestinal and Liver Physiology, Vol 272, Issue 3 617-G625, Copyright © 1997 by American Physiological Society
ARTICLES |
A. J. Makin, R. D. Hughes and R. Williams
Institute of Liver Studies, King's College School of Medicine and Dentistry, London, UK.
Systemic and hepatic circulatory changes were studied in rats over the course of acute liver injury. Hepatic injury was induced by intraperitoneal injection of D-galactosamine (1.1 g/kg), and systemic and hepatic hemodynamics were measured over a 72-h period using a radioactive microsphere technique with direct measurement of arterial, portal venous, and hepatic venous blood oxygen content. Cardiac output increased to a maximum at 48 h, producing a marked increase (450%) in hepatic arterial blood flow so that it became the dominant supply of oxygen at the time of maximal hepatic injury. A subsequent increase in portal venous flow resulted in an overall increase in total hepatic blood flow of 500%. At this point the oxygen delivery by the hepatic arterial and portal venous systems was equal. These circulatory changes returned to control values by 72 h with recovery of liver function. These results demonstrate the development of a hyperdynamic circulation and a marked change in the normal relationship between portal venous and hepatic arterial blood flows that occur during hepatic injury.
This article has been cited by other articles:
![]() |
R Anand, D Harry, S Holt, P Milner, M Dashwood, D Goodier, M Jarmulowicz, and K Moore Endothelin is an important determinant of renal function in a rat model of acute liver and renal failure Gut, January 1, 2002; 50(1): 111 - 117. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |