Related Experiment Video
Updated: Aug 18, 2026

Isolation of Cortical Microglia with Preserved Immunophenotype and Functionality From Murine Neonates
Published on: January 30, 2014
Effects of peroxisome proliferator-activated receptor-gamma agonists on central nervous system inflammation
1Department of Anatomy and Neurobiology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
Abstract:
Peroxisome proliferator-activated receptor-gamma (PPAR-gamma) plays a critical role in glucose and lipid metabolism. More recently, PPAR-gamma ligands have been reported to inhibit the expression of proinflammatory molecules by monocytes/macrophages. Of relevance to CNS disease is that PPAR-gamma agonists have been demonstrated to have similar effects on microglia. PPAR-gamma agonists also ameliorate experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis. This Mini-Review summarizes the effects of PPAR-gamma agonists in mediating immune responses and the potential of these agonists in the treatment of inflammatory disorders of the CNS.
Insights
Peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonists reduce inflammation in brain immune cells and show promise for treating central nervous system inflammatory diseases like multiple sclerosis.
Area of Science:
- Neuroimmunology
- Pharmacology
Background:
- Peroxisome proliferator-activated receptor-gamma (PPAR-gamma) is key in glucose and lipid metabolism.
- PPAR-gamma ligands inhibit inflammatory molecule expression in monocytes/macrophages.
- PPAR-gamma agonists affect microglia, the immune cells of the central nervous system (CNS).
Purpose of the Study:
- To review the role of PPAR-gamma agonists in immune responses.
- To explore the therapeutic potential of PPAR-gamma agonists for CNS inflammatory disorders.
Main Methods:
- Literature review of studies on PPAR-gamma agonists and immune cells.
- Analysis of experimental autoimmune encephalomyelitis (EAE) models.
Main Results:
- PPAR-gamma agonists demonstrate anti-inflammatory effects on microglia.
- PPAR-gamma agonists ameliorate experimental autoimmune encephalomyelitis, a model for multiple sclerosis.
Conclusions:
- PPAR-gamma agonists possess immunomodulatory properties relevant to CNS inflammation.
- PPAR-gamma agonists represent a potential therapeutic strategy for neuroinflammatory diseases.
More Related Videos
07:31Brain Ventricular Microinjections of Lipopolysaccharide into Larval Zebrafish to Assess Neuroinflammation and Neurotoxicity
Published on: August 23, 2022
07:15Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
Published on: August 23, 2024
Related Concept Videos
GPCRs Regulate Adenylyl Cylase Activity
Two...
Transducer Mechanism: Nuclear Receptors
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
Drug-Receptor Interaction: Agonist
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous ligand's action.
Direct-Acting Cholinergic Agonists: Pharmacological Actions
Drugs Acting on Autonomic Ganglia: Stimulants
Ganglionic stimulants activate NM nicotinic receptors in autonomic ganglia, falling into two categories: nicotine mimetics [e.g., lobeline, dimethylpiperazine, tetramethylammonium] and muscarinic receptor agonists [e.g., muscarine, methacholine]. The first category's action is rapid and blocked by nicotinic receptor antagonists, while the second category's action is delayed and blocked by atropine-like agents. Nicotine, an alkaloid, affects the heart rate by stimulating sympathetic or...
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...