Pharmacokinetic and Pharmacodynamc Evaluations of a Potent Analgesic,Dihydroetorphine,in Hairless Rat

摘要

To evaluate the pharmacokinetic and pharmacodynamic char-acteristics of a novel opioid analgesic, dihydroetorphine (DHE), concentrations of DHE and its glucuronide (DG) in plasma and central nervous system (by liquid chromatography-tandem mass spectrometry) and the antinociceptive effect (by tail-im-mersion test) were measured after intravenous (i.v., 2 mg/kg), intracutaneous ((.c., 2 p~g7Kg), subcutaneous (s.c., 2 i~g/kg), intraperitoneal (i.p., 10 jig/kg), and oral (p.o., 200 jig/kg) ad-ministrations in hairless rats. An elimination half-life of plasma DHE concentration was 37.2 mm after i.v. injection. Brain DHE concentration reached a maximum within 6 mm after i.v. injec-tion, and the concentration ratio in brain to plasma was 5.17. Relative bioavailabilities of DHE to i.v. injection (100%) were 70.8,79.8,16.7,and 0.37% after i.c.,s.c.,i.p.,and p.o.administrations, respectively. Area under the plasma concentration-time curve ratios of plasma DG to DHE concentrations after i.v. i.c., s.c., i.p., and p.o. were 1.76, 3.26, 4.74, 14.5, and 290. respectively. Antinociceptive effects appeared rapidly after i.v., l.c., and s.c. administrations but were diminished after i.p. and p.o. administrations, and these effects were ciosely reJated to tfie brain DHE concentrations. DHE was excreted mainly as DG in bile (89.5% of the dose) by 240 mm after i.v. injection. Serum protein binding of DHE was 83.4%, which was not influenced by DG. Glucuronidation of DHE was detected in the liver, in-testine, and kidney in vitro but was minimal in the skin and brain. In conclusion, DHE was rapidly distributed to the brain in relation to producing the antinociceptive effect, and then it was rapidly metabolized to the pharmacologically inactive DG.