1. Academic Validation
  2. Pharmacokinetics of Paradol Analogues Orally Administered to Rats

Pharmacokinetics of Paradol Analogues Orally Administered to Rats

  • J Agric Food Chem. 2016 Mar 9;64(9):1932-7. doi: 10.1021/acs.jafc.5b05615.
Shuichi Setoguchi 1 Daisuke Watase 1 Nami Nagata-Akaho 1 Akinori Haratake 1 Kazuhisa Matsunaga 1 Jiro Takata 1
Affiliations

Affiliation

  • 1 Laboratory of Drug Design and Drug Delivery, Faculty of Pharmaceutical Sciences, Fukuoka University , 19-1 Nanakuma 8-Chome, Jonan-ku, Fukuoka, Japan 814-0180.
Abstract

The kinetics parameters of paradols with different acyl chain lengths have been evaluated to determine their antiobesity site of action. Rats were orally administered olive oil containing 0-, 6-, 8-, or 12-paradol, and blood samples were collected at different time points. The concentrations of the paradols in the plasma were analyzed both with and without β-glucuronidase treatment. The area under the plasma concentration-time curve from 0 to 24 h (AUC(0-24h)) of the parent compounds decreased with increasing acyl chain length. Whereas 12-paradol showed the largest AUC(0-24h) with the longest time to reach its maximum plasma concentration of all of the compounds tested, the AUC(0-24h) values of the metabolites decreased with increasing acyl chain length. These results indicate that increasing acyl chain length leads to a decrease in the absorption of paradols via the intestinal tract, the wall of which was estimated to be their antiobesity site of action.

Keywords

acyl chain length; metabolite; paradol analogue; parent compound; pharmacokinetics.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-14617
    99.42%, COX Inhibitor
    COX