Planta Med 2006; 72(3): 211-216
DOI: 10.1055/s-2005-916195
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Intestinal Absorption of Stemona Alkaloids in a Caco-2 Cell Model

Pak Ho Henry Leung1 , Li Zhang2 , Zhong Zuo2 , Ge Lin1
  • 1Department of Pharmacology, The Chinese University of Hong Kong, Shatin, N. T., Hong Kong, SAR
  • 2School of Pharmacy, The Chinese University of Hong Kong, Shatin, N. T., Hong Kong, SAR
Further Information

Publication History

Received: June 3, 2005

Accepted: August 10, 2005

Publication Date:
05 December 2005 (online)

Abstract

The intestinal absorption of neotuberostemonine and neostenine, two major bioactive alkaloids of the commonly used antitussive traditional Chinese medicine Stemona tuberosa Lour, was investigated using a Caco-2 monolayer model. Both alkaloids exhibited a high absorptive permeability which was higher for neostenine [Papp(AB) = 12.03 ± 1.14 × 10 - 6 cm/s] than for neotuberostemonine [Papp(AB) = 9.27 ± 0.79 × 10 - 6 cm/s], indicating that they are likely to be well absorbed and orally active. Furthermore, both alkaloids were identified to be the substrates of P-glycoprotein and have a transport preference from the basolateral to apical direction with efflux ratios between 2 and 3. Cyclosporin A dose-dependently inhibited the secretory permeability of these alkaloids and abolished their active efflux transport.

References

  • 1 Pilli R A, Ferreira de Oliveira M C. Recent progress in the chemistry of the Stemona alkaloids.  Nat Prod Rep. 2000;  17 117-27
  • 2 Chung H S, Hon P M, Lin G, But P P, Dong H. Antitussive activity of Stemona alkaloids from Stemona tuberosa .  Planta Med. 2003;  69 914-20
  • 3 Chung H S. Chemical and pharmacological investigations into an antitussive traditional Chinese medicinal herb. PhD Thesis. 2001 The Chinese University of Hong Kong Hong Kong, SAR;
  • 4 Artursson P, Palm K, Luthman K. Caco-2 monolayers in experimental and theoretical predictions of drug transport.  Adv Drug Deliv Rev. 2001;  46 27-43
  • 5 Hidalgo I J, Raub T J, Borchardt R T. Characterization of the human colon carcinoma cell line (Caco-2) as a model system for intestinal epithelial permeability.  Gastroenterology. 1989;  96 736-49
  • 6 Meunier V, Bourrie M, Berger Y, Fabre G. The human intestinal epithelial cell line Caco-2; pharmacological and pharmacokinetic applications.  Cell Biol Toxicol. 1995;  11 187-94
  • 7 Chong S, Dando S A, Morrison R A. Evaluation of Biocoat intestinal epithelium differentiation environment (3-day cultured Caco-2 cells) as an absorption screening model with improved productivity.  Pharm Res. 1997;  14 1835-7
  • 8 Zhang L, Zheng Y, Chow M S, Zuo Z. Investigation of intestinal absorption and disposition of green tea catechins by Caco-2 monolayer model.  Int J Pharm. 2004;  287 1-12
  • 9 Vaidyanathan J B, Walle T. Transport and metabolism of the team flavonoid (-)-epicatechin by the human intestinal cell line Caco-2.  Pharm Res. 2001;  18 1420-5
  • 10 Lin G, Li S L, Li P, Chan S W. Chromatographic analysis of Fritillaria isosteroidal alkaloids, the active principles of Beimu, the antitussive traditional Chinese medicinal herb.  J Chromatogr A. 2001;  935 321-38
  • 11 Li S L, Lin G, Chan S W, Li P. Determination of the major isosteroidal alkaloids in Bulbs of Fritillaria by high performance liquid chromatography coupled with evaporative light scattering detector.  J Chromatogr A. 2001;  909 207-14
  • 12 Gunnarsson T, Karlsson A, Hansson P, Johnson G, Alling C, Odham G. Determination of phosphatidylethanol in blood from alcoholic males using high-performance liquid chromatography and evaporative light scattering or electrospray mass spectrometric detection.  J Chromatogr B. 1998;  705 243-9
  • 13 Niemi R, Taipale H, Ahlmark M, Vepsäläinen J, Järvinen T. Simultaneous determination of clodronate and its partial ester derivatives by ion-pair reversed-phase high-performance liquid chromatography coupled with evaporative light-scattering detection.  J Chromatogr B. 1997;  701 97-102
  • 14 Artursson P, Karlsson J. Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells.  Biochem Biophys Res Commun. 1991;  175 880-5
  • 15 Collett A, Sims E, Walker D, He Y L, Ayrton J. Comparison of HT29 - 18-C1 and Caco-2 cell lines as models for studying intestinal paracellular drug absorption.  Pharm Res. 1996;  13 216-21
  • 16 Artursson P, Ungell A L, Lofroth J E. Selective paracellular permeability in two models of intestinal absorption: cultured monolayers of human intestinal epithelial cells and rat intestinal segments.  Pharm Res. 1993;  10 1123-9
  • 17 Gutmann H, Fricker G, Torok M, Michael S, Beglinger C. Evidence for different ABC-transporters in Caco-2 cells modulating drug uptake.  Pharm Res. 1999;  16 402-7
  • 18 Gollapudi S, Kim C H, Tram B, Sangha S, Gupta S. Probenecid reverse multidrug resistance in multidrug resistance-associated protein-overexpressing HL60/AR and H69/AR cells but not in P-glycoprotein-overexpressing HL60/Tax and P388/ARD cells.  Cancer Chemother Pharmacol. 1997;  40 150-8
  • 19 Kim R B, Former M F, Wandel C, Leake B, Wood A J, Roden D M. et al . The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors.  J Clin Invest. 1998;  101 289-94
  • 20 Braun A, Hammerle S, Suda K, Rothen-Rutishauser B, Gunthert M, Kramer S D. et al . Cell cultures as tools in biopharmacy.  Eur J Pharm Sci. 2000;  Suppl 2 S51-60
  • 21 Faassen F, Vogel G, Spanings H, Vromans H. Caco-2 permeability, P-glycoprotein transport ratios and brain penetration of heterocyclic drugs.  Int J Pharm. 2003;  263 113-22

Ge Lin, Ph. D.

Department of Pharmacology

Faculty of Medicine

The Chinese University of Hong Kong

Shatin

N. T.

Hong Kong

SAR

Phone: +852-2609-6824

Fax: +852-2603-5139

Email: linge@cuhk.edu.hk

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