Food dyes as P-glycoprotein modulators

  • Jack W. Staples
  • , Jessica M. Stine
  • , Eero Mäki-Lohiluoma
  • , Emily Steed
  • , Kathleen M. George
  • , Charles M. Thompson
  • , Erica L. Woodahl

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

The drug transporter P-glycoprotein (P-gp) is often investigated in drug-interaction studies because the activity is modulated by a wide variety of xenobiotics including drugs, herbal products, and food components. In this study, we tested six common arylsulfonate food dyes—allura red, carmoisine, ponceau 4R, quinolone yellow, sunset yellow, and tartrazine—as activators and inhibitors of P-gp activity in vitro. The dyes were studied as P-gp activators by measuring ATPase activity in P-gp-expressing membranes. Compared to verapamil, a known activator of P-gp, the six food dyes showed no stimulatory activity. The potential for these six food dyes to act as P-gp inhibitors was tested in an intracellular efflux assay with P-gp-expressing cells. Compared to GF120918, a known P-gp inhibitor, there was no inhibitory activity for these six food dyes. The six food dyes tested do not interact with P-gp in vitro and, therefore, are unlikely cause clinical drug-food dye interactions. Further investigation is necessary to determine whether these food dyes could interact with other drug transporters.

Original languageEnglish
Article number111785
JournalFood and Chemical Toxicology
Volume146
DOIs
StatePublished - Dec 2020

Funding

The authors would like to thank Rachel Burmeister, Rachel Dalton, Erin Ellerbeck, and Joachim Veit for training and consultation on initial experimental design, and the Skaggs School of Pharmacy at the University of Montana for the support of pharmacy student research. This work was support by the Center for Biomolecular Structure and Dynamics under a grant by National Institutes of Health ( P20GM103546 ). The authors would like to thank Rachel Burmeister, Rachel Dalton, Erin Ellerbeck, and Joachim Veit for training and consultation on initial experimental design, and the Skaggs School of Pharmacy at the University of Montana for the support of pharmacy student research. This work was support by the Center for Biomolecular Structure and Dynamics under a grant by National Institutes of Health (P20GM103546).

FundersFunder number
Center for Biomolecular Structure and Dynamics
P20GM103546

    Keywords

    • Drug transporter
    • Food dye
    • P-glycoprotein

    Fingerprint

    Dive into the research topics of 'Food dyes as P-glycoprotein modulators'. Together they form a unique fingerprint.

    Cite this