HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Changes in Radixin Expression and Interaction with Efflux Transporters in the Liver of Adjuvant-Induced Arthritic Rats.

Abstract
Scaffold proteins such as radixin help to modulate the plasma membrane localization and transport activity of the multidrug resistance-associated protein 2 (MRP2/ABCC2) and P-glycoprotein (P-gp/ABCB1) efflux transporters in the liver. We examined changes in radixin expression and interaction with efflux transporters in adjuvant-induced arthritic (AA) rats, an animal model of rheumatoid arthritis, as well as in human liver cancer (HepG2) cells because inflammation affects drug pharmacokinetics via the efflux transporters. The expression levels of radixin and phosphorylated radixin (p-radixin) were measured 24 h after treatment with inflammatory cytokines comprising tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6 or sodium nitroprusside (SNP; a nitric oxide donor). The protein levels of radixin, MRP2, and P-gp in the rat liver were next examined. We also investigated whether inflammation affected the formation of complexes between radixin and MRP2 or P-gp. The mRNA and protein levels of radixin in HepG2 cells were significantly decreased by TNF-α treatment, while minimal changes were observed after treatment with IL-1β, IL-6 or SNP. TNF-α also significantly decreased the protein levels of p-radixin, suggesting that TNF-α inhibited the activation of radixin and thereby reduced the activity of the efflux transporters. Complex formation of radixin with MRP2 and P-gp was significantly decreased in AA rats but this was reversed by prednisolone and dexamethasone treatment, indicating that decreased interactions of radixin with MRP2 and P-gp likely occur during liver inflammation. These data suggest that liver inflammation reduces radixin function by decreasing its interactions with MRP2 and P-gp.
AuthorsAtsushi Kawase, Misaki Nakasaka, Hatsune Bando, Saori Yasuda, Hiroaki Shimada, Masahiro Iwaki
JournalInflammation (Inflammation) Vol. 43 Issue 1 Pg. 85-94 (Feb 2020) ISSN: 1573-2576 [Electronic] United States
PMID31654296 (Publication Type: Journal Article)
Chemical References
  • ABCC2 protein, human
  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • ATP-Binding Cassette Transporters
  • Abcc2 protein, rat
  • Anti-Inflammatory Agents
  • Cytokines
  • Cytoskeletal Proteins
  • Membrane Proteins
  • Multidrug Resistance-Associated Protein 2
  • Nitric Oxide Donors
  • radixin
Topics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 (metabolism)
  • ATP-Binding Cassette Transporters (metabolism)
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Arthritis, Experimental (genetics, metabolism, microbiology)
  • Cytokines (pharmacology)
  • Cytoskeletal Proteins (genetics, metabolism)
  • Female
  • Hep G2 Cells
  • Humans
  • Liver (drug effects, metabolism)
  • Membrane Proteins (genetics, metabolism)
  • Multidrug Resistance-Associated Protein 2
  • Mycobacterium
  • Nitric Oxide Donors (pharmacology)
  • Phosphorylation
  • Protein Binding
  • Rats, Sprague-Dawley

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: