Differential modulation of FXR activity by chlorophacinone and ivermectin analogs

Toxicol Appl Pharmacol. 2016 Dec 15:313:138-148. doi: 10.1016/j.taap.2016.10.017. Epub 2016 Oct 20.

Abstract

Chemicals that alter normal function of farnesoid X receptor (FXR) have been shown to affect the homeostasis of bile acids, glucose, and lipids. Several structural classes of environmental chemicals and drugs that modulated FXR transactivation were previously identified by quantitative high-throughput screening (qHTS) of the Tox21 10K chemical collection. In the present study, we validated the FXR antagonist activity of selected structural classes, including avermectin anthelmintics, dihydropyridine calcium channel blockers, 1,3-indandione rodenticides, and pyrethroid pesticides, using in vitro assay and quantitative structural-activity relationship (QSAR) analysis approaches. (Z)-Guggulsterone, chlorophacinone, ivermectin, and their analogs were profiled for their ability to alter CDCA-mediated FXR binding using a panel of 154 coregulator motifs and to induce or inhibit transactivation and coactivator recruitment activities of constitutive androstane receptor (CAR), liver X receptor alpha (LXRα), or pregnane X receptor (PXR). Our results showed that chlorophacinone and ivermectin had distinct modes of action (MOA) in modulating FXR-coregulator interactions and compound selectivity against the four aforementioned functionally-relevant nuclear receptors. These findings collectively provide mechanistic insights regarding compound activities against FXR and possible explanations for in vivo toxicological observations of chlorophacinone, ivermectin, and their analogs.

Keywords: Chlorophacinone; Diphacinone; Farnesoid X receptor; Ivermetin; Moxidectin; Nuclear receptor; Tox21.

MeSH terms

  • HEK293 Cells
  • Humans
  • Indans / pharmacology*
  • Ivermectin / analogs & derivatives
  • Ivermectin / pharmacology*
  • Receptors, Cytoplasmic and Nuclear / drug effects*
  • Structure-Activity Relationship

Substances

  • Indans
  • Receptors, Cytoplasmic and Nuclear
  • farnesoid X-activated receptor
  • chlorophacinone
  • Ivermectin