Metabolism and Disposition of Myristicin in the Isolated Perfused Rat Liver

  • Jeong, Chang Kyun (Bioanalysis Laboratory, College of Pharmacy and Medicinal Resources Research Center, Wonkwang University) ;
  • Kim, Kyun (Toxicology Research Center, Korea Research Institute of Chemical Technology) ;
  • Lee, Hye Suk (Bioanalysis Laboratory, College of Pharmacy and Medicinal Resources Research Center, Wonkwang University)
  • Received : 2001.09.21
  • Published : 2001.12.31

Abstract

To investigate the hepatic metabolism of myristicin isolated rat livers were perfused under single-pass conditions with perfusate containing myristicin. In outflow perfusate and bile, 5-allyl-1-methoxy-2,3-dihydroxybenzene (M1), M1-sulfate, and M1-glucuronide conjugates were identified as the metabolites of myristicin. HPLC method with UV detection was applied to investigate the hepatic disposition of the compounds. The concentration of myristicin, M1, and M1-conjugates in the outflow perfusate reached steady-state levels within 20 min after commencing the perfusion of $4.5{\mu}M$ myristicin. At steady-state, the mean (${\pm}S.D.$) extraction ratio of myristicin was $0.49({\pm}0.16)$ and clearance was $13.7({\pm}4.5)ml/min$. M1 accounted for $44.0{\pm}5.3%$ of eliminated myristicin and was recovered as unchanged M1, M1-sulfate, and M1-glucuronide in the bile and outflow perfusate.

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