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Xenobiotica
the fate of foreign compounds in biological systems
Volume 50, 2020 - Issue 8
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Xenobiotic Transporters

Metabolism and disposition of corylifol A from Psoralea corylifolia: metabolite mapping, isozyme contribution, species differences and identification of efflux transporters for corylifol A-O-glucuronide in HeLa1A1 cells

, , , , , , , & show all
Pages 997-1008 | Received 30 Dec 2019, Accepted 17 Feb 2020, Published online: 01 Apr 2020
 

Abstract

  1. Corylifol A (CA), a phenolic compound from Psoralea corylifolia, possessed several biological properties but poor bioavailability. Here we aimed to investigate the roles of cytochromes P450s (CYPs), UDP-glucuronosyltransferases (UGTs) and efflux transporters in metabolism and disposition of CA.

  2. Metabolism of CA was evaluated in HLM, expressed CYPs and UGTs. Chemical inhibitors and shRNA-mediated gene silencing of multidrug resistance-associated proteins (MRPs) and breast cancer resistance protein (BCRP) were performed to assess the roles of transporters in CA disposition.

  3. Three oxidated metabolites (M1–M3) and two glucuronides (M4–M5) were detected. The intrinsic clearances (CLint) values of M1 and M4 in HLM were 48.10 and 184.03 μL/min/mg, respectively. Additionally, CYP1A1, 2C8 and 2C19 were identified as main contributors with CLint values of 13.01–49.36 μL/min/mg, while UGT1A1, 1A7, 1A8 and 1A9 were with CLint values ranging from 85.01 to 284.07 μL/min/mg. Furthermore, activity correlation analysis proved CYP2C8, UGT1A1 and 1A9 were the main active hepatic isozymes. Besides, rats and monkeys were appropriate model animals. Moreover, dipyridamole and MK571 both could significantly inhibit M4 efflux. Gene silencing results also indicated MRP4 and BCRP were major contributors in HeLa1A1 cells.

  4. Taken together, CYPs, UGTs, MRP4 and BCRP were important determinants of CA pharmacokinetics.

Disclosure statement

All the authors have reported no declarations of interest.

Additional information

Funding

This work was supported by State Key Laboratory of Drug Research [SIMM1903KF-07], Guangdong Basic and Applied Basic Research Foundation [2019A1515011285], Foundation of He’nan Educational Committee [20A350012], National Natural Science Foundation of China [81903704], Program of Introducing Talents of Discipline to Universities [B13038], State Key Program of National Natural Science Foundation of China [81630097] and Major Project for International Cooperation and Exchange of the National Natural Science Foundation of China [81220108028].

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