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PPARγ, neuroinflammation, and disease
BACKGROUND: Peroxisome proliferator-activated receptors (PPARs) are a class of nuclear transcription factors that are activated by fatty acids and their derivatives. One of these, PPARγ, regulates responsiveness to insulin in adipose cells, and PPARγ-activating drugs such as pioglitazone are used in...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC483058/ https://www.ncbi.nlm.nih.gov/pubmed/15285797 http://dx.doi.org/10.1186/1742-2094-1-5 |
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author | Mrak, Robert E Landreth, Gary E |
author_facet | Mrak, Robert E Landreth, Gary E |
author_sort | Mrak, Robert E |
collection | PubMed |
description | BACKGROUND: Peroxisome proliferator-activated receptors (PPARs) are a class of nuclear transcription factors that are activated by fatty acids and their derivatives. One of these, PPARγ, regulates responsiveness to insulin in adipose cells, and PPARγ-activating drugs such as pioglitazone are used in the treatment of type 2 diabetes. PPARγ acts in myeloid-lineage cells, including T-cells and macrophages, to suppress their activation and their elaboration of inflammatory molecules. PPARγ activation also suppresses the activated phenotype in microglia, suggesting that PPARγ-activating drugs may be of benefit in chronic neuroinflammatory diseases. Some, but not all, nonsteroidal anti-inflammatory agents (indomethacin and ibuprofen in particular) also have activating effects on PPARγ. DISCUSSION AND CONCLUSIONS: These observations suggest on the one hand a role for PPARγ-activating drugs in the treatment of chronic neuroinflammatory diseases-as shown for a patient with secondary progressive multiple sclerosis by Pershadsingh et al. in this issue of the Journal of Neuroinflammation-and suggest on the other hand a possible explanation for confusing and contradictory results in trials of nonsteroidal anti-inflammatory agents in Alzheimer's disease. |
format | Text |
id | pubmed-483058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4830582004-07-26 PPARγ, neuroinflammation, and disease Mrak, Robert E Landreth, Gary E J Neuroinflammation Commentary BACKGROUND: Peroxisome proliferator-activated receptors (PPARs) are a class of nuclear transcription factors that are activated by fatty acids and their derivatives. One of these, PPARγ, regulates responsiveness to insulin in adipose cells, and PPARγ-activating drugs such as pioglitazone are used in the treatment of type 2 diabetes. PPARγ acts in myeloid-lineage cells, including T-cells and macrophages, to suppress their activation and their elaboration of inflammatory molecules. PPARγ activation also suppresses the activated phenotype in microglia, suggesting that PPARγ-activating drugs may be of benefit in chronic neuroinflammatory diseases. Some, but not all, nonsteroidal anti-inflammatory agents (indomethacin and ibuprofen in particular) also have activating effects on PPARγ. DISCUSSION AND CONCLUSIONS: These observations suggest on the one hand a role for PPARγ-activating drugs in the treatment of chronic neuroinflammatory diseases-as shown for a patient with secondary progressive multiple sclerosis by Pershadsingh et al. in this issue of the Journal of Neuroinflammation-and suggest on the other hand a possible explanation for confusing and contradictory results in trials of nonsteroidal anti-inflammatory agents in Alzheimer's disease. BioMed Central 2004-05-14 /pmc/articles/PMC483058/ /pubmed/15285797 http://dx.doi.org/10.1186/1742-2094-1-5 Text en Copyright © 2004 Mrak and Landreth; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Commentary Mrak, Robert E Landreth, Gary E PPARγ, neuroinflammation, and disease |
title | PPARγ, neuroinflammation, and disease |
title_full | PPARγ, neuroinflammation, and disease |
title_fullStr | PPARγ, neuroinflammation, and disease |
title_full_unstemmed | PPARγ, neuroinflammation, and disease |
title_short | PPARγ, neuroinflammation, and disease |
title_sort | pparγ, neuroinflammation, and disease |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC483058/ https://www.ncbi.nlm.nih.gov/pubmed/15285797 http://dx.doi.org/10.1186/1742-2094-1-5 |
work_keys_str_mv | AT mrakroberte ppargneuroinflammationanddisease AT landrethgarye ppargneuroinflammationanddisease |