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Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update

Alzheimer’s disease (AD) is an age-related progressive neurodegenerative disorder, characterized by the deposition of amyloid-β within the brain parenchyma resulting in a significant decline in cognitive functions. The pathophysiological conditions of the disease are recognized by the perturbation o...

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Autores principales: Khan, Mahmood Ahmad, Alam, Qamre, Haque, Absarul, Ashafaq, Mohammad, Khan, Mohd Jahir, Ashraf, Ghulam Md, Ahmad, Mahboob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425074/
https://www.ncbi.nlm.nih.gov/pubmed/30152284
http://dx.doi.org/10.2174/1570159X16666180828100002
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author Khan, Mahmood Ahmad
Alam, Qamre
Haque, Absarul
Ashafaq, Mohammad
Khan, Mohd Jahir
Ashraf, Ghulam Md
Ahmad, Mahboob
author_facet Khan, Mahmood Ahmad
Alam, Qamre
Haque, Absarul
Ashafaq, Mohammad
Khan, Mohd Jahir
Ashraf, Ghulam Md
Ahmad, Mahboob
author_sort Khan, Mahmood Ahmad
collection PubMed
description Alzheimer’s disease (AD) is an age-related progressive neurodegenerative disorder, characterized by the deposition of amyloid-β within the brain parenchyma resulting in a significant decline in cognitive functions. The pathophysiological conditions of the disease are recognized by the perturbation of synaptic function, energy and lipid metabolism. In Addition deposition of amyloid plaques also triggers inflammation upon the induction of microglia. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors known to play important role in the regulation of glucose ab-sorption, homeostasis of lipid metabolism and are further known to involved in repressing the expression of genes related to inflammation. Therefore, agonists of this receptor represent an attractive therapeutic target for AD. Recently, both clinical and preclinical studies showed that use of Peroxisome proliferator-activated receptor gamma (PPARγ) agonist improves both learning and memory along with other AD related pathology. Thus, PPARγ signifies a significant new therapeutic target in treating AD. In this review, we have shed some light on the recent progress of how, PPARγ agonist selectively modulated different cellular targets in AD and its amazing potential in the treatment of AD.
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spelling pubmed-64250742019-09-01 Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update Khan, Mahmood Ahmad Alam, Qamre Haque, Absarul Ashafaq, Mohammad Khan, Mohd Jahir Ashraf, Ghulam Md Ahmad, Mahboob Curr Neuropharmacol Article Alzheimer’s disease (AD) is an age-related progressive neurodegenerative disorder, characterized by the deposition of amyloid-β within the brain parenchyma resulting in a significant decline in cognitive functions. The pathophysiological conditions of the disease are recognized by the perturbation of synaptic function, energy and lipid metabolism. In Addition deposition of amyloid plaques also triggers inflammation upon the induction of microglia. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors known to play important role in the regulation of glucose ab-sorption, homeostasis of lipid metabolism and are further known to involved in repressing the expression of genes related to inflammation. Therefore, agonists of this receptor represent an attractive therapeutic target for AD. Recently, both clinical and preclinical studies showed that use of Peroxisome proliferator-activated receptor gamma (PPARγ) agonist improves both learning and memory along with other AD related pathology. Thus, PPARγ signifies a significant new therapeutic target in treating AD. In this review, we have shed some light on the recent progress of how, PPARγ agonist selectively modulated different cellular targets in AD and its amazing potential in the treatment of AD. Bentham Science Publishers 2019-03 2019-03 /pmc/articles/PMC6425074/ /pubmed/30152284 http://dx.doi.org/10.2174/1570159X16666180828100002 Text en © 2019 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Khan, Mahmood Ahmad
Alam, Qamre
Haque, Absarul
Ashafaq, Mohammad
Khan, Mohd Jahir
Ashraf, Ghulam Md
Ahmad, Mahboob
Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update
title Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update
title_full Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update
title_fullStr Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update
title_full_unstemmed Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update
title_short Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimer's Disease: An Update
title_sort current progress on peroxisome proliferator-activated receptor gamma agonist as an emerging therapeutic approach for the treatment of alzheimer's disease: an update
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425074/
https://www.ncbi.nlm.nih.gov/pubmed/30152284
http://dx.doi.org/10.2174/1570159X16666180828100002
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