<abstract xmlns="http://www.w3.org/1999/xhtml"> This study was aimed at investigating the effect of ethanol on oral bioavailability of kaempferol in rats, namely, at disclosing their possible interaction. Kaempferol (100 or 250 mg kg-1 bm) was administered to the rats by oral gavage with or without ethanol (600 mg kg-1 bm) co-administration. Intravenous administration (10 and 25 mg kg-1 bm) of kaempferol was used to determine the bioavailability. The concentration of kaempferol in plasma was estimated by ultra high performance liquid chromatography. During coadministration, a significant increase of the area under the plasma concentration-time curve as well as the peak concentration were observed, along with a dramatic decrease in total body clearance. Consequently, the bioavailability of kaempferol in oral control groups was 3.1 % (100 mg kg-1 bm) and 2.1 % (250 mg kg-1 bm). The first was increased by 4.3 % and the other by 2.8 % during ethanol co-administration. Increased permeability of cell membrane and ethanolkaempferol interactions on CYP450 enzymes may enhance the oral bioavailability of kaempferol in rats.</abstract>

This study was aimed at investigating the effect of ethanol on oral bioavailability of kaempferol in rats, namely, at disclosing their possible interaction. Kaempferol (100 or 250 mg kg-1 bm) was administered to the rats by oral gavage with or without ethanol (600 mg kg-1 bm) co-administration. Intravenous administration (10 and 25 mg kg-1 bm) of kaempferol was used to determine the bioavailability. The concentration of kaempferol in plasma was estimated by ultra high performance liquid chromatography. During coadministration, a significant increase of the area under the plasma concentration-time curve as well as the peak concentration were observed, along with a dramatic decrease in total body clearance. Consequently, the bioavailability of kaempferol in oral control groups was 3.1 % (100 mg kg-1 bm) and 2.1 % (250 mg kg-1 bm). The first was increased by 4.3 % and the other by 2.8 % during ethanol co-administration. Increased permeability of cell membrane and ethanolkaempferol interactions on CYP450 enzymes may enhance the oral bioavailability of kaempferol in rats.

Pharmacokinetic evaluation of the interaction between oral kaempferol and ethanol in rats

College of Veterinary Medicine Northwest A&F University, Yangling Shaanxi 712100,

School of Pharmacy Xi’an Jiaotong University Xi’an Shaanxi 710061,

Acta Pharmaceutica

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

This study was aimed at investigating the effect of ethanol on oral bioavailability of kaempferol in rats, namely, at disclosing their possible interaction....

Pharmacokinetic evaluation of the interaction between oral kaempferol and ethanol in rats

Online veröffentlicht: 15. Okt. 2016

Seitenbereich: 563 - 568

Akzeptiert: 25. Juli 2016

DOI: https://doi.org/10.1515/acph-2016-0044

Schlüsselwörter
kaempferol, bioavailability, pharmacokinetics, ethanol, cytochrome P450s

© by Xiaoying Zhang

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Pharmacokinetic evaluation of the interaction between oral kaempferol and ethanol in rats

Online veröffentlicht: 15. Okt. 2016

Seitenbereich: 563 - 568

Akzeptiert: 25. Juli 2016

DOI: https://doi.org/10.1515/acph-2016-0044

Schlüsselwörterkaempferol, bioavailability, pharmacokinetics, ethanol, cytochrome P450s

© by Xiaoying Zhang

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Schlüsselwörter
kaempferol, bioavailability, pharmacokinetics, ethanol, cytochrome P450s