Peroxisome Proliferator-Activated Receptors and Shock State

Author:

Esposito Emanuela12,Cuzzocrea Salvatore23,Meli Rosaria1

Affiliation:

1. Department of Experimental Pharmacology, University of Naples “Federico II”, Naples, Italy

2. IRCCS Centro Neurolesi “Bonino-Pulejo”, Messina, Italy

3. Department of Clinical and Experimental Medicine and Pharmacology, Torre Biologica Policlinico Universitario, Messina, Italy

Abstract

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear hormone receptor superfamily of ligand-activated transcription factors that are related to retinoid, steroid, and thyroid hormone receptors. Three isotypes of PPARs have been identified: alpha, beta/delta, and gamma, encoded by different genes and distributed in various tissues. PPARs are implicated in the control of inflammatory responses and in energy homeostasis and, thus, can be defined as metabolic and anti-inflammatory transcription factors. They exert anti-inflammatory effects by inhibiting the induction of proinflammatory cytokines, adhesion molecules, and extracellular matrix proteins, or by stimulating the production of anti-inflammatory molecules. Moreover, PPARs modulate the proliferation, differentiation, and survival of immune cells. This review presents the current state of knowledge regarding the involvement of PPARs in the control of inflammatory response, and their potential therapeutic applications in several types of shock, as well as hemorrhagic, septic, and nonseptic shock.

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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