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Amelioration of experimental autoimmune encephalomyelitis in C57BL/6 mice by an agonist of peroxisome proliferator-activated receptor-gamma.

Abstract
Peroxisome proliferator-activated receptor-gamma (PPAR-gamma), a member of the nuclear hormone receptor superfamily, plays a critical role in adipocyte differentiation and glucose homeostasis. It has been implicated that PPAR-gamma functions as a regulator of cellular proliferation and inflammatory responses. In the present study, we examined whether troglitazone, a selective PPAR-gamma agonists, ameliorated experimental autoimmune encephalomyelitis (EAE) induced by administration of myelin oligodendrocyte glycoprotein (MOG) peptide 35-55 in C57BL/6 mice. We found that troglitazone attenuated the inflammation and decreased the clinical symptoms. It was suggested that the amelioration was attributed to the attenuation of pro-inflammatory cytokine gene expressions.
AuthorsM Niino, K Iwabuchi, S Kikuchi, M Ato, T Morohashi, A Ogata, K Tashiro, K Onoé
JournalJournal of neuroimmunology (J Neuroimmunol) Vol. 116 Issue 1 Pg. 40-8 (May 01 2001) ISSN: 0165-5728 [Print] Netherlands
PMID11311328 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Chromans
  • Cytokines
  • Inflammation Mediators
  • Mog protein, mouse
  • Myelin Proteins
  • Myelin-Associated Glycoprotein
  • Myelin-Oligodendrocyte Glycoprotein
  • Peptide Fragments
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Thiazoles
  • Thiazolidinediones
  • Transcription Factors
  • Troglitazone
Topics
  • Animals
  • Cell Division (drug effects)
  • Chromans (pharmacology)
  • Cytokines (genetics)
  • Encephalomyelitis, Autoimmune, Experimental (immunology, pathology, prevention & control)
  • Female
  • Inflammation Mediators (physiology)
  • Mice
  • Mice, Inbred C57BL
  • Myelin Proteins
  • Myelin-Associated Glycoprotein (immunology)
  • Myelin-Oligodendrocyte Glycoprotein
  • Peptide Fragments (immunology)
  • RNA, Messenger (antagonists & inhibitors)
  • Receptors, Cytoplasmic and Nuclear (agonists)
  • Reference Values
  • T-Lymphocytes (pathology)
  • Thiazoles (pharmacology)
  • Thiazolidinediones
  • Transcription Factors (agonists)
  • Troglitazone

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