Planta Med 2012; 78(09): 909-913
DOI: 10.1055/s-0031-1298517
Pharmacokinetic Investigations
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

First-pass Metabolism of Decursin, a Bioactive Compound of Angelica gigas, in Rats

Hyun Seo Park
1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, South Korea
,
Byunghyun Kim
1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, South Korea
,
Ju-Hee Oh
1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, South Korea
,
Young Choong Kim
2   College of Pharmacy, Seoul National University, Seoul, South Korea
,
Young-Joo Lee
1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, South Korea
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 09. März 2012
revised 10. April 2012

accepted 15. April 2012

Publikationsdatum:
09. Mai 2012 (online)

Abstract

Decursin is considered the major bioactive compound of Angelica gigas roots, a popular Oriental herb and dietary supplement. In this study, the pharmacokinetics of decursin and its active metabolite, decursinol, were evaluated after the administration of decursin in rats. The plasma concentration of decursin decreased rapidly, with an initial half-life of 0.05 h. It was not detectable at 1 h after intravenous administration at an area under the plasma concentration-time curve of 1.20 µg · mL−1·h, whereas the concentration of decursinol increased rapidly reaching a maximum concentration of 2.48 µg · mL−1 at the time to maximum plasma concentration of 0.25 h and an area under the plasma concentration-time curve of 5.23 µg · mL−1·h. Interestingly, after oral administration of decursin, only decursinol was present in plasma, suggesting an extensive hepatic first-pass metabolism of decursin. The extremely low bioavailability of decursin after its administration via the hepatic portal vein (the fraction of dose escaping first-pass elimination in the liver, FH = 0.11) is indicative of extensive hepatic first-pass metabolism of decursin, which was confirmed by a tissue distribution study. These findings suggest that decursin is not directly associated with the bioactivity of A. gigas and that it may work as a type of natural prodrug of decursinol.

Supporting Information

 
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