Targeting Nuclear Hormone Receptors: PPARαAgonists as Potential Disease-Modifying Drugs for Rheumatoid Arthritis
Author(s) -
I. V. Shirinsky,
V. S. Shirinsky
Publication year - 2011
Publication title -
international journal of rheumatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.8
H-Index - 33
eISSN - 1687-9279
pISSN - 1687-9260
DOI - 10.1155/2011/937843
Subject(s) - rheumatoid arthritis , medicine , nuclear receptor , peroxisome proliferator activated receptor , ppar agonist , inflammation , receptor , bioinformatics , pharmacology , lipid metabolism , arthritis , thiazolidinedione , disease , hormone , endocrinology , transcription factor , biology , diabetes mellitus , biochemistry , gene , type 2 diabetes
In recent years, peroxisome proliferator-activated receptors (PPARs) have received growing interest due to the broad spectrum of their biological activities. PPAR α , an isoform of PPAR, plays an important role in lipid homeostasis and inflammation, which makes it a potential target for the treatment of chronic inflammatory disorders, including RA. This paper reviews studies on the properties of PPAR α agonists which may be pertinent to the treatment of RA. These properties include effects on lipid metabolism, inflammation, and angiogenesis, as well as interference with glucocorticoid effects, and a potential role in gender dimorphism of autoimmune disorders. However, current clinical experience with this class of drugs in RA is limited. New studies are needed to elucidate whether PPAR α agonism may be an effective treatment strategy for RA patients.
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