Planta Med 2007; 73(5): 444-450
DOI: 10.1055/s-2007-967178
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Effects of Schisandra Lignans on P-Glycoprotein-Mediated Drug Efflux in Human Intestinal Caco-2 Cells

Hye Hyun Yoo1 , Mijin Lee1 , Min Woo Lee1 , Sun Young Lim1 , Jongheon Shin2 , Dong-Hyun Kim1
  • 1Bioanalysis and Biotransformation Research Center, Korea Institute of Science and Technology, Seoul, Korea
  • 2Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul, Korea
Further Information

Publication History

Received: September 12, 2006 Revised: February 20, 2007

Accepted: March 12, 2007

Publication Date:
16 April 2007 (online)

Abstract

Schisandra fruits (Schisandraceae) are often used in traditional medicine and can be taken concomitantly with conventional medicine. In this study, the effects of dibenzocyclooctadiene lignans from Schizandra chinensis on P-gp-mediated efflux were examined to investigate a possible interaction with P-gp substrates. The cellular accumulation of rhodamine-123 in Caco-2 cells was measured with 12 Schisandra lignans. Most compounds resulted in slight or moderate increases of rhodamin-123 cellular uptake, indicating their P-gp inhibitory activity. Among them, deoxyschizandrin exhibited the most potent effect on the accumulation of rhodamine-123. Subsequently, bidirectional transports of digoxin and rhodamine-123 in Caco-2 cells were determined with deoxyschizandrin, the most active compound for the rhodamine-123 assay. In the bidirectional transport study, apical-to-basal (A-to-B) transports of digoxin and rhodamine-123 were increased, whereas basal-to-apical (B-to-A) transports were decreased by deoxyschizandrin in concentration- and time-dependent manners. At 50 μM of deoxyschizandrin, the transport ratios (B-A/A-B) for digoxin and rhodamine-123 were 2.2 and 2.1 compared with the control ratios of 15.2 and 12.2, respectively. These results demonstrated that deoxyschizandrin effectively inhibited the P-gp-mediated efflux in Caco-2 cells, suggesting they could potentially increase the absorption of drugs that can act as a P-gp substrate.

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Dr. Dong-Hyun Kim

Bioanalysis and Biotransformation Research Center

Korea Institute of Science and Technology

P.O. Box 131

Chungryang

Seoul

Korea

Phone: +82-2-958-5055

Fax: +82-2-958-5059

Email: dhkim@kist.re.kr

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