Cited by 62Peroxisome Proliferator-Activated ReceptorsParaoxonase enzyme and polymorphismsAdipose Tissue and Metabolism

Biology and Therapeutic Applications of Peroxisome Proliferator- Activated Receptors

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P. Menendez-Gutierrez, Maria, Roszer, Tamas, Ricote, Mercedes·2012·Current Topics in Medicinal Chemistry

Abstract

Peroxisome proliferator-activated receptors (PPARs) are ligand dependent transcription factors. The three mammalian PPARs are key regulators of fatty acid and lipoprotein metabolism, glucose homeostasis, cellular proliferation/ differentiation and the immune response. PPARs are therefore important targets in the treatment of metabolic disorders such as insulin resistance and type 2 diabetes mellitus, and are also of interest in relation to chronic inflammatory diseases such as atherosclerosis, arthritis, chronic pulmonary inflammation, pancreatitis, inflammatory bowel disease, and psoriasis. Recent advances have attributed novel functions to PPARs in blood pressure regulation, neuroinflammation, nerve-cell protection, inflammatory pain reduction, and the hypothalamic control of metabolism. The abundant pleiotropic actions of PPARs suggest that PPAR agonists have enormous therapeutic potential. However, current PPAR-based therapies often have undesired side effects due to the concomitant activation of PPARs in non-target cells. There is therefore growing interest in the development of cell-specific PPAR agonists and improvement of the clinical use of PPAR ligands. This review gives an overview of PPAR functions and discusses the current and potential medical implications of PPAR ligands in various pathologies, ranging from metabolic disorders to cardiovascular disease, chronic inflammation, neurodegenerative disorders and cancer. Keywords: Nuclear receptors, PPAR, transcription, metabolism, inflammation, cardiovascular disease, neuroinflammation, cancer, lipoprotein metabolism, glucose homeostasis, insulin resistance, type 2 diabetes mellitus, atherosclerosis, arthritis, chronic pulmonary inflammation, inflammatory bowel disease

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Crossref · 10.2174/156802612799436669

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  • Thiazolidinediones act as agonists of peroxisome proliferator-activated receptor gamma and exert neuroprotective effects, reducing oxidative stress and weakening the pro-inflammatory response, as well as promoting neuroplasticity via increased production of brain-derived neurotrophic factor.

    “Thiazolidinediones act as agonists of peroxisome proliferator-activated receptor gamma and have been demonstrated to exert neuroprotective effects, reducing oxidative stress and weakening the pro-inflammatory response, as well as promoting neuroplasticity via increased production of BDNF [116].”

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References 428 · Cited by 62

Authors
P. Menendez-Gutierrez, M., Roszer, T., & Ricote, M.
Affiliations
Spanish National Centre for Cardiovascular Research (ES)
Corresponding author
Ricote, Mercedes
Venue
Current Topics in Medicinal Chemistry
Published
2012-03-01
Volume
12
Issue
6
Pages
548-584
ISSN
1568-0266 (ISSN-L)
OpenAlex
W2122671044
Cited by
62
References
428
Citations by year
2025: 1 · 2024: 5 · 2022: 2 · 2021: 3 · 2020: 10 · 2019: 4 · 2018: 1 · 2017: 8 · 2016: 7 · 2015: 6 · 2014: 5 · 2013: 6 · 2012: 4
FWCI
2.70
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Current Topics in Medicinal Chemistry (publishedVersion)
  • PubMed (publishedVersion)
  • LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by-nc-nd)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Paraoxonase enzyme and polymorphisms
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
Keywords
peroxisome proliferator-activated receptors, PPAR agonists, nuclear receptors, ligand-dependent transcription, lipoprotein metabolism, glucose homeostasis, insulin resistance, type 2 diabetes, atherosclerosis, arthritis, chronic lung inflammation, inflammatory bowel disease, psoriasis, neuroinflammation, blood pressure regulation, cardiovascular disease, cancer, neurodegenerative diseases, inflammatory pain
MeSH terms
Animals, Humans, Ligands, Peroxisome Proliferator-Activated Receptors, Molecular Targeted Therapy

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