Effects of naringenin on the pharmacokinetics of tofacitinib in rats

Pharm Biol. 2020 Dec;58(1):225-230. doi: 10.1080/13880209.2020.1738504.

Abstract

Context: Naringenin and tofacitinib are often used together for treatment of rheumatoid arthritis in Chinese clinics.Objective: This experiment investigates the effect of naringenin on the pharmacokinetics of tofacitinib in rats.Materials and methods: Twelve Sprague-Dawley rats were randomly divided into two groups (experimental group and control group). The experimental group was pre-treated with naringenin (150 mg/kg/day) for two weeks before dosing tofacitinib, and equal amounts of CMC-Na solution in the control group. After a single oral administration of 5 mg/kg of tofacitinib, 50 μL blood samples were directly collected into 1.5 mL heparinized tubes via the caudal vein at 0.083, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 and 24 h. The plasma concentration of tofacitinib was quantified by UPLC/MS-MS.Results: Results indicated that naringenin could significantly affect the pharmacokinetics of tofacitinib. The AUC0-24 of tofacitinib was increased from 1222.81 ± 222.07 to 2016.27 ± 481.62 ng/mL/h, and the difference was significant (p < 0.05). Compared with the control group, the Tmax was increased from 0.75 ± 0.29 to 3.00 ± 0.00 h (p < 0.05), and the MRT(0-24) was increased from 4.90 ± 0.51 to 6.57 ± 0.66 h (p < 0.05), but the clearance was obviously decreased from 4.10 ± 0.72 to 2.42 ± 0.70 L/h/kg (p < 0.05) in experimental group. Although the Cmax and t1/2 of tofacitinib were increased, there were no significant differences (p > 0.05).Conclusions: This research demonstrated a drug-drug interaction between naringenin and tofacitinib possibly when preadministered with naringenin; thus, we should pay attention to this possibility in the clinic.

Keywords: CYP3A4; Drug–drug interaction; flavonoids.

MeSH terms

  • Administration, Oral
  • Animals
  • Anti-Inflammatory Agents / administration & dosage
  • Anti-Inflammatory Agents / pharmacokinetics*
  • Anti-Inflammatory Agents / pharmacology*
  • Area Under Curve
  • Arthritis, Rheumatoid / drug therapy
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Female
  • Flavanones / administration & dosage
  • Flavanones / pharmacology*
  • Piperidines / administration & dosage
  • Piperidines / blood
  • Piperidines / pharmacokinetics*
  • Piperidines / pharmacology*
  • Pyrimidines / administration & dosage
  • Pyrimidines / blood
  • Pyrimidines / pharmacokinetics*
  • Pyrimidines / pharmacology*
  • Pyrroles / administration & dosage
  • Pyrroles / blood
  • Pyrroles / pharmacokinetics*
  • Pyrroles / pharmacology*
  • Rats, Sprague-Dawley
  • Signal-To-Noise Ratio

Substances

  • Anti-Inflammatory Agents
  • Flavanones
  • Piperidines
  • Pyrimidines
  • Pyrroles
  • tofacitinib
  • naringenin

Grants and funding

This work was supported by grants funded by the Natural Science Foundation of Zhejiang and Zhejiang Pharmaceutical Association Joint Foundation [LYY18H280003] and the High-Level Talent Training Project of Lishui [2017RC21].