Evaluation of drug interactions of Saposhnikoviae Radix and its major components with astragaloside IV and paeoniflorin using in vitro and in vivo experiments

J Chromatogr A. 2024 May 24:1723:464716. doi: 10.1016/j.chroma.2024.464716. Epub 2024 Feb 3.

Abstract

Saposhnikoviae Radix (SR) may enhance the pharmacodynamics of Huangqi Chifeng Tang (HQCFT) in the treatment of cerebral infarction according to our previous research, but the underlying mechanism is unknown. Herein, an in vivo pharmacokinetic assay in rats and in vitro MDCK-MDR1 cell assays were used to investigate the possible mechanism of SR, its main components, and its interactions with Astragali Radix (AR) and Paeoniae Radix (PR). An ultrahigh-performance liquid chromatography-tandem mass spectrometry (UPLC‒MS/MS)-based analytical method for quantifying astragaloside IV (ASIV) and paeoniflorin (PAE) in microdialysis and transport samples was developed. The pharmacokinetic parameters of SR were determined using noncompartmental analyses CCK-8 assays were used to detect the cytotoxicity of ASIV, PAE, cimifugin (CIM), prim-o-glucosylcimifugin (POG) and their combinations. Moreover, drug transport was studied using MDCK-MDR1 cells. Western blotting was performed to measure the protein expression levels of P-GP and MRP1. Claudin-5, ZO-1, and F-actin expression was determined via immunohistochemical staining of MDCK-MDR1 cells. harmacokinetic studies revealed that, compared with those of Huangqi Chifeng Tang-Saposhnikoviae Radix (HQCFT-SR), the Tmax of ASIV increased by 11.11 %, and the MRT0-t and Tmax of PAE increased by 11.19 % and 20 %, respectively, in the HQCFT group. Transport studies revealed that when ASIV was coincubated with 28 μM CIM or POG, the apparent permeability coefficient (Papp) increased by 71.52 % and 50.33 %, respectively. Coincubation of PAE with 120 μM CIM or POG increased the Papp by 87.62 % and 60.95 %, respectively. Moreover, CIM and POG significantly downregulated P-gp and MRP1 (P < 0.05), inhibited the expression of Claudin-5, ZO-1, and F-actin (P < 0.05), and affected intercellular tight junctions (TJs). In conclusion, our study successfully established a selective, sensitive and reproducible UPLC‒MS/MS analytical method to detect drug‒drug interactions between SR, AR and PR in vivo and in vitro, which is beneficial for enhancing the therapeutic efficacies of AR and PR. Moreover, this study provides a theoretical basis for further research on the use of SR as a drug carrier.

Keywords: Astragaloside IV; Blood–brain barrier; Cimifugin; Paeoniflorin; Prim-o-glucosylcimifugin.

MeSH terms

  • Animals
  • Apiaceae / chemistry
  • Chromatography, High Pressure Liquid / methods
  • Dogs
  • Drug Interactions
  • Drugs, Chinese Herbal* / chemistry
  • Drugs, Chinese Herbal* / pharmacokinetics
  • Drugs, Chinese Herbal* / pharmacology
  • Glucosides* / analysis
  • Glucosides* / chemistry
  • Glucosides* / pharmacokinetics
  • Glucosides* / pharmacology
  • Herb-Drug Interactions
  • Madin Darby Canine Kidney Cells
  • Male
  • Monoterpenes* / analysis
  • Rats
  • Rats, Sprague-Dawley*
  • Reproducibility of Results
  • Saponins* / analysis
  • Saponins* / chemistry
  • Saponins* / pharmacokinetics
  • Saponins* / pharmacology
  • Tandem Mass Spectrometry* / methods
  • Triterpenes* / analysis
  • Triterpenes* / chemistry
  • Triterpenes* / pharmacokinetics
  • Triterpenes* / pharmacology

Substances

  • peoniflorin
  • astragaloside A
  • Glucosides
  • Saponins
  • Monoterpenes
  • Triterpenes
  • Drugs, Chinese Herbal