From: HubMed - breast cancer <rssfwd@rssfwd.com>
Date: Sun, Apr 27, 2008 at 2:55 AM
Subject: Inhibitory effects of terpenoids on multidrug resistance-associated protein 2- and breast cancer resistance protein-mediated transport.
To: mesothelioma77@gmail.com
[1]Drug Metab Dispos. 2008 Apr 24;
Yoshida N, Takada T, Yamamura Y, Adachi I, Suzuki H, Kawakami J
The possibility of interactions between natural products/supplements and conventional prescription medicines is one of the most important issues in pharmacotherapeutic safety. Recently, we reported that some terpenoids such as (R)-(+)-citronellal and glycyrrhetic acid, which are present in herbal medicines, can act as inhibitors of P-glycoprotein (MDR1/ABCB1). In the present study, the effects of seven terpenoids on multidrug resistance-associated protein 2 (MRP2/ABCC2) and breast cancer resistance protein (BCRP/ABCG2)-mediated transport were investigated in vitro. Membrane vesicles were prepared from MRP2 cDNA transfected Sf9 cells derived from pupal ovarian tissue of Spodoptera frugiperda, a fall armyworm, and BCRP cDNA transfected LLC-PK1 cells derived from porcine kidney. MRP2 or BCRP-mediated efflux transport was measured as ATP-dependent accumulation of [(3)H]estradiol 17-beta-D-glucuronide (E217betaG) into membrane vesicles collected by a rapid filtration technique. The effects of (R)-(+)-citronellal, (S)-(-)-beta-citronellol, alpha-terpinene, terpinolene, (-)-beta-pinene, abietic acid and glycyrrhetic acid on the intravesicular accumulation of [(3)H]E217betaG were examined. Large decreases in the [(3)H]E217betaG accumulation into vesicles from MRP2-expressing Sf9 cells were observed in the presence of glycyrrhetic acid and abietic acid, and their IC50 values were about 20 microM and 51 microM, respectively. [(3)H]E217betaG accumulation into vesicles from BCRP-overexpressing LLC-PK1 cells was suppressed by only glycyrrhetic acid, with an IC50 value of about 39 microM. Other terpenoids used in this study did not alter the ATP-dependent accumulation of [(3)H]E217betaG. These findings suggest that glycyrrhetic acid and abietic acid can potently inhibit MRP2- or BCRP-mediated membrane transport and may interact with their substrates in pharmacokinetic processes.
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Source: http://www.hubmed.org/display.cgi?uids=18436619
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