Relationship between hepatic mitochondrial functions in vivo and in vitro in rats with carbon tetrachloride-induced liver cirrhosis

Background/Aims: The metabolic capacity of liver mitochondria is impaired in rats with carbon tetrachloride (CCl4)-induced cirrhosis. These studies mere performed to find out whether benzoate and/or palmitate are suitable substrates for assessing hepatic mitochondrial function in vivo. Methods: In vivo metabolism of benzoate and 1-C-14-palmitate mas assessed by monitoring urinary excretion of hippurate and exhalation of (CO2)-C-14, respectively, in cirrhotic and control rats (n=8 for each group), Isolation of liver mitochondria, and in vitro benzoate and palmitate metabolism mere performed by methods published previously The hepatic content of mitochondria was assessed by stereological analysis of the volume of hepatocytes and by biochemical determination, using the activity of citrate synthase. Results: Renal excretion of hippurate following i.p. administration of benzoate was reduced in cirrhotic rats (64+/-15 vs. 85+/-14% of administered dose over 24 h), and showed a linear correlation with hippurate formation by isolated mitochondria, The activities of benzoyl-CoA synthase and benzoyl-CoA:glycine N-acyltransferase mere reduced by approximately 60%, and the coenzyme A content by 50% in hepatic mitochondria from cirrhotic rats, explaining impaired hippurate formation, Peak exhalation of (CO2)-C-14 after i.p, administration of 1-C-14-palmitate was reduced by 44% and the area under the (CO2)-C-14 exhalation-time curve by 34% in cirrhotic rats, Peak (CO2)-C-14 exhalation revealed a linear correlation with oxidative metabolism of palmitoylcarnitine in isolated mitochondria, Both in vivo benzoate and palmitate metabolism showed a linear correlation with the volume fraction of hepatocytes, The mitochondrial protein content mas reduced in cirrhotic rats per g liver and per liver but equal to control rats per volume of hepatocytes. Conclusions: In vivo metabolism of both palmitate and benzoate reflects hepatic mitochondrial function in rats with CCl4-induced cirrhosis, Hepatic mitochondrial function is impaired in rats with CCl4-induced cirrhosis due to both reduced mitochondrial volume per liver and impaired metabolism of the remaining mitochondria. In contrast to rats with secondary biliary cirrhosis, rats with CCl4-induced cirrhosis showed no hepatic mitochondrial proliferation to counteract reduced mitochondrial function.