Troglitazone acts by PPARgamma and PPARgamma-independent pathways on LLC-PK1-F+ acid-base metabolism

Am J Physiol Renal Physiol. 2004 Jan;286(1):F100-10. doi: 10.1152/ajprenal.00182.2003. Epub 2003 Sep 23.

Abstract

Troglitazone was studied in pH-sensitive LLC-PK1-F+ cells to determine the effect on pHi and glutamine metabolism as well as the role of peroxisome proliferator-activated receptor (PPARgamma)-dependent and PPARgamma-independent signaling pathways. Troglitazone induces a dose-dependent cellular acidosis that occurs within 4 min and persists over 18 h as a result of inhibiting Na+/H+ exchanger-mediated acid extrusion. Cellular acidosis was associated with glutamine-dependent augmented [15N]ammonium production and decreased [15N]alanine formation from 15N-labeled glutamine. The shift in glutamine metabolism from alanine to ammoniagenesis appears within 3 h and is associated after 18 h with both a reduction in assayable alanine aminotransferase (ALT) activity as well as cellular acidosis. The relative contribution of troglitazone-induced cellular acidosis vs. the decrease in assayable ALT activity to alanine production could be demonstrated. The PPARgamma antagonist bisphenol A diglycide ether (BADGE) reversed both the troglitazone-induced cellular acidosis and ammoniagenesis but enhanced the troglitazone reduction of assayable ALT activity; BADGE also blocked troglitazone induction of peroxisome proliferator response element-driven firefly luciferase activity. The protein kinase C (PKC) inhibitor chelerythrine mimics troglitazone effects, whereas phorbol ester reverses the effects on ammoniagenesis consistent with troglitazone negatively regulating the DAG/PKC/ERK pathway. Although functional PPARgamma signaling occurs in this cell line, the major troglitazone-induced acid-base responses appear to be mediated by pathway(s) involving PKC/ERK.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acid-Base Equilibrium / drug effects*
  • Acid-Base Equilibrium / physiology
  • Acidosis / chemically induced
  • Alanine / metabolism
  • Alkaloids
  • Animals
  • Antineoplastic Agents / pharmacology*
  • Benzhydryl Compounds
  • Benzophenanthridines
  • Carcinogens / pharmacology
  • Chromans / pharmacology*
  • Enzyme Inhibitors / pharmacology
  • Epoxy Compounds / pharmacology
  • Genes, Reporter
  • Hydrogen-Ion Concentration / drug effects
  • LLC-PK1 Cells
  • Phenanthridines / pharmacology
  • Plasmids
  • Protein Kinase C / antagonists & inhibitors
  • Quaternary Ammonium Compounds / metabolism
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Swine
  • Thiazolidinediones / pharmacology*
  • Transcription Factors / metabolism*
  • Troglitazone

Substances

  • Alkaloids
  • Antineoplastic Agents
  • Benzhydryl Compounds
  • Benzophenanthridines
  • Carcinogens
  • Chromans
  • Enzyme Inhibitors
  • Epoxy Compounds
  • Phenanthridines
  • Quaternary Ammonium Compounds
  • Receptors, Cytoplasmic and Nuclear
  • Thiazolidinediones
  • Transcription Factors
  • chelerythrine
  • Protein Kinase C
  • 2,2-bis(4-glycidyloxyphenyl)propane
  • Troglitazone
  • Alanine