Planta Med 2004; 70(2): 138-142
DOI: 10.1055/s-2004-815490
Original Paper
Biochemistry
© Georg Thieme Verlag Stuttgart · New York

Extremely Low Bioavailability of Magnesium Lithospermate B, An Active Component from Salvia miltiorrhiza, in Rat

Ying Zhang1 , 2 , 3 , Teruaki Akao1 , Norio Nakamura4 , Chang-Ling Duan2 , Masao Hattori4 , Xiu-Wei Yang3 , Jian-Xun Liu2
  • 1Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Toyama, Japan
  • 2Xiyuan Hospital, China Academy of Traditional Chinese Medicine, Beijing, P. R. China
  • 3Department of Pharmacy, Beijing University, Beijing, P. R. China
  • 4Research Institute of Oriental Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan
Further Information

Publication History

Received: July 7, 2003

Accepted: October 25, 2003

Publication Date:
02 March 2004 (online)

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Abstract

We assessed the bioavailability of magnesium lithospermate B (MLB), a main polyphenolic component of Salvia miltiorrhiza and a potent antioxidant having various pharmacological activities, to evaluate its action in vivo. The plasma concentrations of lithospermic acid B (LSB) showed a biexponential decrease after intravenous administration of MLB to rats at doses of 4 and 20 mg/kg. The values of area under the concentration-time curve (AUC; 87.8 ± 10.9 and 1130 ± 329 μg·min/mL), total body clearance (CLtot; 55.52 ± 7.07 and 23.51 ± 5.98 mL/min/kg), and distribution volume at steady state (Vss; 7.60 ± 1.03 and 3.61 ± 1.16 L/kg) suggested non-linear pharmacokinetics between the two doses. After oral administration of MLB at a high dose of 100 mg/kg, the mean AUC was barely 1.26 ± 0.36 μg·min/mL. Absolute bioavailability of MLB was calculated to be 0.0002 from the AUC values after both intravenous dosing at 20 mg/kg and oral dosing at 100 mg/kg. The extremely low bioavailability was caused mainly by poor absorption from the rat gastrointestinal tract; about 65 % of the dose was retained in the tract even 4 h after oral administration, and most of the dose was retained even 20 min after infusion in an in situ jejunal loop experiment. Urinary and biliary excretion of LSB were only 0.70 % ± 0.26 % and 5.10 % ± 2.36 %, respectively, over a 30 h time period after intravenous injection despite the large CLtot and Vss values, and were much less (0.010 % ± 0.001 % and 0.12 % ± 0.04 %) after oral dosing. These findings suggest that extensive metabolism, including a first-pass effect, and wide distribution of LSB besides the poor absorption contributed significantly to the extremely low systemic bioavailability.

References

Dr. T. Akao

Faculty of Pharmaceutical Sciences

Toyama Medical and Pharmaceutical University

2630 Sugitani

Toyama 930-0194

Japan

Email: taO113@ms.toyama-mpu.ac.jp