JTZ-951 (enarodustat), a hypoxia-inducibe factor prolyl hydroxylase inhibitor, stabilizes HIF-α protein and induces erythropoiesis without effects on the function of vascular endothelial growth factor

Eur J Pharmacol. 2019 Sep 15:859:172532. doi: 10.1016/j.ejphar.2019.172532. Epub 2019 Jul 10.

Abstract

JTZ-951 (enarodustat) is an oral hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor. JTZ-951 has inhibitory activities on human HIF-prolyl hydroxylase 1-3, but not on various receptors or enzymes. In Hep3B cells, JTZ-951 increased HIF-1α and HIF-2α protein levels, erythropoietin (EPO) mRNA levels, and EPO production. In normal rats, after a single oral dose of JTZ-951, the hepatic and renal EPO mRNA levels and plasma EPO concentrations were also increased. In 5/6-nephrectomized rats, repeated oral doses of JTZ-951 once daily or intermittent dosing showed the erythropoiesis stimulating effect. The administration of JTZ-951 at a high dose increased plasma vascular endothelial growth factor (VEGF) levels; however, retinal VEGF mRNA levels and the retinal vascular permeability were not changed. Finally, we evaluated the effect of JTZ-951 in a colorectal cancer cell-inoculated mouse model. Although JTZ-951 at a high dose increased the plasma VEGF, it had no effect on tumor growth. In summary, JTZ-951 induces erythropoiesis without affecting VEGF function. Therefore, it is expected that JTZ-951 will be a new oral candidate that increases and maintains hemoglobin concentrations in renal anemia patients.

Keywords: Erythropoietin; Hypoxia-inducible factor prolyl hydroxylase inhibitor; JTZ-951 (enarodustat); Renal anemia; Vascular endothelial growth factor.

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Cell Line
  • Dose-Response Relationship, Drug
  • Erythropoiesis / drug effects*
  • Erythropoietin / genetics
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Hypoxia-Inducible Factor-Proline Dioxygenases / antagonists & inhibitors*
  • N-substituted Glycines / pharmacology*
  • Prolyl-Hydroxylase Inhibitors / pharmacology*
  • Protein Stability / drug effects
  • Pyridines / pharmacology*
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Triazoles / pharmacology*
  • Vascular Endothelial Growth Factor A / biosynthesis
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • N-substituted Glycines
  • Prolyl-Hydroxylase Inhibitors
  • Pyridines
  • RNA, Messenger
  • Triazoles
  • Vascular Endothelial Growth Factor A
  • Erythropoietin
  • endothelial PAS domain-containing protein 1
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • enarodustat