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Nitric oxide induced sinusoidal relaxation after a propranolol priming dose in the perfused rat liver reduces propranolol availability on subsequent dosing
Author(s) -
Liu Xin,
Zou Yuhong,
Khlentzos Alexander M,
Yang Yan,
Nikolovski Julijana,
Weiss Michael,
Roberts Michael S
Publication year - 2010
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/j.1440-1681.2010.05434.x
Subject(s) - propranolol , pharmacokinetics , pharmacology , chemistry , nitric oxide , nitric oxide synthase , pharmacodynamics , bolus (digestion) , endocrinology , medicine
Summary 1. The present study sought to explain the mechanism leading to reduced availability of propranolol when given after a priming dose in the single‐pass perfused rat liver. 2. Extracellular sucrose space (as a measure of sinusoidal relaxation) in perfused rat liver before and after propranolol or propranolol and N G ‐nitro‐ l ‐arginine methyl ester ( l ‐NAME; nitric oxide (NO) synthase inhibitor) treatment were examined. The results showed that propranolol induces sinusoidal relaxation in the perfused liver and this effect could be abolished by NO synthase inhibitor l ‐NAME. 3. Two bolus injections of propranolol were given to the isolated perfused rat liver and outflow concentration‐time profiles of intact propranolol were determined. A two‐phase physiologically based organ pharmacokinetic model was applied to estimate hepatocellular influx, efflux, binding, ion‐trapping and metabolic elimination pharmacokinetic parameters for propranolol. The recovery of propranolol in the second injection was approximately 54% of that in the first injection. The permeability‐surface area product, the binding and the intrinsic clearance all increased significantly after prior exposure of the rat liver to the first bolus of propranolol ( P < 0.05). 4. Based on the findings of the present study, we propose that the most likely explanation for the reduced availability of a second propranolol dose (after administration of a priming dose) in the perfused liver is a consequence of the NO‐mediated sinusoidal relaxation effect of propranolol, arising from the priming dose. This observation supports the view that the pharmacokinetics of some drugs might be altered by the pharmacodynamic effects of the same drug given earlier in the perfused liver.