Irinotecan (CPT-11) is a semisynthetic derivative of camptothecine that has proved activity in the treatment of colorectal carcinoma. The metabolites identi®ed in humans include SN-38, SN-38 glucuronide, and several CYP3A-derived metabolites. We have studied the hepatic extraction, metabolism, and b
Clearance by the liver in cirrhosis. I. Relationship between propranolol metabolism in vitro and its extraction by the perfused liver in the rat
✍ Scribed by Daphna Fenyves; Louise Gariépy; Dr. Jean-Pierre Villeneuve
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 743 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
✦ Synopsis
To delineate the factors responsible for impaired clearance in cirrhosis, we examined propranolol dis- position in rats with carbon tetrachloride-induced cirrhosis and compared it with that in control animals, rats treated with chlorpromazine (an inhibitor of propranolol metabolism) and rats with acute liver injury. We measured the extraction ratio of propranolol by the isolated perfused liver and related it to estimates of propranolol drug-metabolizing enzyme activity in homogenates of the same livers. In control animals, drug-metabolizing enzyme activity (measured as the ratio V,,/KJ averaged 5,319 f 1,193 ml/min; the extraction ratio in the perfused liver was close to 1.0 (0.97 f 0.01). Important decreases of microsomal enzyme activity were observed in rats treated with chlorpromazine (30 f 27 ml/min, p < 0.001) and in rats with acute liver injury (724 f 401 ml/min, p < 0.001), accounting for the decrease in the hepatic extraction ratio by the perfused liver (0.33 f 0.09 and 0.71 f 0.04, respectively, p < 0.01). In cirrhotic livers, enzyme activity was not significantly different from that of controls (3,592 f 1,857 ml/min) and could not account for the observed decrease in extraction (0.66 f 0.14, p < 0.01). The extraction of antipyrine by the isolated perfused liver was also measured as an index of microsomal enzyme activity and related to propranolol extraction. Antipyrine extraction was decreased by 90% in acute liver injury, compared with 33% in cirrhosis, suggesting a much greater reduction of microsomal enzyme activity in the former group. Despite these differences, the extraction ratio of propranolol was reduced to a similar extent in rats with cirrhosis (0.64 2 0.20) and in rats with acute liver injury (0.77 2 0.10) compared with controls (0.97 2 0.02). These results suggest that factors other than decreased enzyme activity (i.e., impaired uptake) con-
📜 SIMILAR VOLUMES
We studied the steady-state hepatic extraction and single-pass hepatic uptake of propranolol in isolated perfused livers from normal rats and compared these values with those of rats with carbon tetrachlorideinduced cirrhosis, rats treated with chlorpromazine (an inhibitor of propranolol metabolism)
The metabolism and biliary excretion of i4C-dideoxyinosine (I4C-ddI) has been investigated using the in situ perfused rat liver (PRL) preparation. After 2 h of perfusion through the liver, approximately 7&75 per cent of the total I4C-radiolabel was recovered in the perfusion medium, less than 1 per
The kinetics of hepatic elimination of the high-clearance drug propranolol has been interpreted in a previous study from our laboratory, in which propranolol protein binding was varied, to conform to the venous equilibrium model. In another study by a different group, in which perfusate flow was var