| Literature DB >> 26296158 |
Chukwuemezie Chimezie1, Adina Ewing1, Chandler Schexnayder1, Melyssa Bratton1, Elena Glotser1, Elena Skripnikova1, Pedro Sá2, Stephen Boué3, Robert E Stratford4.
Abstract
Glyceollins are phytoalexins produced in soybeans under stressful growth conditions. On the basis of prior evaluations, they show potential to treat multiple diseases, including certain cancers, Type 2 diabetes, and cardiovascular conditions. The aim of the present study was to expand on recent studies designed to initially characterize the intestinal disposition of glyceollins. Specifically, studies were undertaken in Caco-2 cells to evaluate glyceollins' effects on apical efflux transporters, namely, MRP2 and BCRP, which are the locus of several intestinal drug-drug and drug-food interactions. 5- (and 6)-carboxy-2',7'-dichloroflourescein (CDF) was used to provide a readout on MRP2 activity, whereas BODIPY-prazosin provided an indication of BCRP alteration. Glyceollins were shown to reverse MRP2-mediated CDF transport asymmetry in a concentration-dependent manner, with activity similar to the MRP2 inhibitor, MK-571. Likewise, they demonstrated concentration-dependent inhibition of BCRP-mediated efflux of BODIPY-prazosin with a potency similar to that of Ko143. Glyceollin did not appreciably alter MRP2 or BCRP expression following 24 h of continuous exposure. The possibility that glyceollin mediated inhibition of genistein metabolite efflux by either transporter was evaluated. However, results demonstrated an interaction at the level of glyceollin inhibition of genistein metabolism rather than inhibition of metabolite transport.Entities:
Keywords: active transport; drug interaction; efflux pumps; flavonoids; food effects; genistein; glyceollin; intestinal absorption; intestinal metabolism; phytoestrogen
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Year: 2016 PMID: 26296158 PMCID: PMC4761526 DOI: 10.1002/jps.24605
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534