Planta Med 2009; 75(6): 631-634
DOI: 10.1055/s-0029-1185387
Pharmacology
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Intestinal Permeability of Antitumor Alkaloids from the Processed Seeds of Strychnos nux-vomica in a Caco-2 Cell Model

Lian Ma1 , Xiu-Wei Yang1 , Wei Xu1 , Bao-Chang Cai2 , Masao Hattori3
  • 1State Key Laboratory of Natural and Biomimetic Drugs and Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University, Beijing, P. R. China
  • 2Nanjing University of Traditional Chinese Medicine, Nanjing, P. R. China
  • 3Division of Metabolic Engineering, Institute of Natural Medicine, University of Toyama, Sugitani, Toyama, Japan
Further Information

Publication History

received November 5, 2008 revised December 14, 2008

accepted December 21, 2008

Publication Date:
23 February 2009 (online)

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Abstract

The uptake and intestinal permeability of the seven alkaloids strychnine (Str), brucine (Bru), β-colubrine (Col), strychnine N-oxide (S‐N), brucine N-oxide (B–N), pseudostrychnine (Psd), and icajine (Ica), which were isolated from the processed seeds of Strychnos nux-vomica L., were investigated in the human intestinal Caco-2 model. Determination of compounds was carried out by HPLC. The apparent permeability coefficients (P app) for Str, Bru, Col, S‐N, B–N, Psd, and Ica in the apical-to-basolateral direction were (3.11 ± 0.17) × 10−5, (1.67 ± 0.65) × 10−5, (2.67 ± 0.30) × 10−5, (0.17 ± 0.01) × 10−5, (0.35 ± 0.02) × 10−5, (2.51 ± 0.33) × 10−5, and (2.61 ± 0.34) × 10−5 cm/s, respectively. In the concentration range of 10–200 µM, Str, Bru, Col, and Psd showed substantial concentration-dependent transport across the monolayers. The transports of all seven alkaloids were linear with time and showed moderate to high permeabilities. In the presence of 2,4-dinitrophenol or sodium azide, the P app of Ica was reduced significantly in both the apical-to-basolateral and basolateral-to-apical directions. The dominant mechanism of the intestinal absorption for Str, Bru, Col, S‐N, B–N, and Psd was passive diffusion, while it was partially ATP dependent for Ica.

References

Prof. Dr. Xiu-Wei Yang

State Key Laboratory of Natural and Biomimetic Drugs and Department of Natural Medicines
School of Pharmaceutical Sciences
Peking University

No. 38 Xueyuan Road, Haidian District

Beijing 100191

People's Republic of China

Phone: + 86 10 82 80 51 06

Fax: + 86 10 82 80 27 24

Email: xwyang@bjmu.edu.cn