Studies on pharmacokinetic properties and absorption mechanism of phloretin: In vivo and in vitro.

Yuan Yuan Zhao, Yu Fan, Mei Wang, Jing Wang, Jiang Xue Cheng, Jun Bo Zou, Xiao Fei Zhang, Ya Jun Shi, Dong Yan Guo

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2020 Dec

filter terms:

Phloretin is a natural dihydrochalcone flavonoid that is mainly distributed in apple, pear and other juicy fruit peels or root peels. Phloretin exhibits several pharmacological properties, such as antidiabetic, antioxidant, anti-inflammatory, and antitumor activities. However, the poor water solubility of phloretin limits its application in the treatment of numerous diseases. To date, the underlying mechanisms of phloretin absorption have not been investigated. In this study, the pharmacokinetics of phloretin orally administered to Sprague-Dawley (SD) rats were examined, and the absorption mechanisms of phloretin were investigated in a Caco-2 cell monolayer and single-pass intestinal perfusion in SD rat. The effects measured by basic parameters, such as compound concentration, time, temperature, paracellular pathway, in different intestinal segments were analyzed, and various inhibitors, such as the P-glycoprotein (P-gp) inhibitor verapamil, the multidrug resistance protein 2 (MRP2) inhibitor indomethacin, the breast cancer resistance protein (BCRP) inhibitor reserpine, and the closely related regulator EDTA, were evaluated to determine their effects on the absorption of phloretin. The pharmacokinetics of phloretin was studied by oral and intravenous injection in rats. The bioavailability was 8.676 %.The SPIP experiments showed that P-gp, MRP2, BCRP protein inhibitor and closely related regulator, could significantly increase the apparent permeability coefficient (Papp) of phloretin. Monolayer transport experiments in Caco-2 cells showed that P-gp, MRP2 protein inhibitor and closely related regulator EDTA, significantly increased the Papp value of phloretin. In conclusion, phloretin is a substrate of P-gp and MRP2, and its modes of transport include active transport, efflux protein transport and cell bypass. Copyright © 2020 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Citation

Yuan Yuan Zhao, Yu Fan, Mei Wang, Jing Wang, Jiang Xue Cheng, Jun Bo Zou, Xiao Fei Zhang, Ya Jun Shi, Dong Yan Guo. Studies on pharmacokinetic properties and absorption mechanism of phloretin: In vivo and in vitro. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2020 Dec;132:110809