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Natural products, PGC-1α, and Duchenne muscular dystrophy

Peroxisome proliferator-activated receptor γ (PPARγ) is a transcriptional coactivator that binds to a diverse range of transcription factors. PPARγ coactivator 1 (PGC-1) coactivators possess an extensive range of biological effects in different tissues, and play a key part in the regulation of the o...

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Autores principales: Suntar, Ipek, Sureda, Antoni, Belwal, Tarun, Sanches Silva, Ana, Vacca, Rosa Anna, Tewari, Devesh, Sobarzo-Sánchez, Eduardo, Nabavi, Seyed Fazel, Shirooie, Samira, Dehpour, Ahmad Reza, Xu, Suowen, Yousefi, Bahman, Majidinia, Maryam, Daglia, Maria, D'Antona, Giuseppe, Nabavi, Seyed Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276681/
https://www.ncbi.nlm.nih.gov/pubmed/32528825
http://dx.doi.org/10.1016/j.apsb.2020.01.001
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author Suntar, Ipek
Sureda, Antoni
Belwal, Tarun
Sanches Silva, Ana
Vacca, Rosa Anna
Tewari, Devesh
Sobarzo-Sánchez, Eduardo
Nabavi, Seyed Fazel
Shirooie, Samira
Dehpour, Ahmad Reza
Xu, Suowen
Yousefi, Bahman
Majidinia, Maryam
Daglia, Maria
D'Antona, Giuseppe
Nabavi, Seyed Mohammad
author_facet Suntar, Ipek
Sureda, Antoni
Belwal, Tarun
Sanches Silva, Ana
Vacca, Rosa Anna
Tewari, Devesh
Sobarzo-Sánchez, Eduardo
Nabavi, Seyed Fazel
Shirooie, Samira
Dehpour, Ahmad Reza
Xu, Suowen
Yousefi, Bahman
Majidinia, Maryam
Daglia, Maria
D'Antona, Giuseppe
Nabavi, Seyed Mohammad
author_sort Suntar, Ipek
collection PubMed
description Peroxisome proliferator-activated receptor γ (PPARγ) is a transcriptional coactivator that binds to a diverse range of transcription factors. PPARγ coactivator 1 (PGC-1) coactivators possess an extensive range of biological effects in different tissues, and play a key part in the regulation of the oxidative metabolism, consequently modulating the production of reactive oxygen species, autophagy, and mitochondrial biogenesis. Owing to these findings, a large body of studies, aiming to establish the role of PGC-1 in the neuromuscular system, has shown that PGC-1 could be a promising target for therapies targeting neuromuscular diseases. Among these, some evidence has shown that various signaling pathways linked to PGC-1α are deregulated in muscular dystrophy, leading to a reduced capacity for mitochondrial oxidative phosphorylation and increased reactive oxygen species (ROS) production. In the light of these results, any intervention aimed at activating PGC-1 could contribute towards ameliorating the progression of muscular dystrophies. PGC-1α is influenced by different patho-physiological/pharmacological stimuli. Natural products have been reported to display modulatory effects on PPARγ activation with fewer side effects in comparison to synthetic drugs. Taken together, this review summarizes the current knowledge on Duchenne muscular dystrophy, focusing on the potential effects of natural compounds, acting as regulators of PGC-1α.
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spelling pubmed-72766812020-06-10 Natural products, PGC-1α, and Duchenne muscular dystrophy Suntar, Ipek Sureda, Antoni Belwal, Tarun Sanches Silva, Ana Vacca, Rosa Anna Tewari, Devesh Sobarzo-Sánchez, Eduardo Nabavi, Seyed Fazel Shirooie, Samira Dehpour, Ahmad Reza Xu, Suowen Yousefi, Bahman Majidinia, Maryam Daglia, Maria D'Antona, Giuseppe Nabavi, Seyed Mohammad Acta Pharm Sin B Review Peroxisome proliferator-activated receptor γ (PPARγ) is a transcriptional coactivator that binds to a diverse range of transcription factors. PPARγ coactivator 1 (PGC-1) coactivators possess an extensive range of biological effects in different tissues, and play a key part in the regulation of the oxidative metabolism, consequently modulating the production of reactive oxygen species, autophagy, and mitochondrial biogenesis. Owing to these findings, a large body of studies, aiming to establish the role of PGC-1 in the neuromuscular system, has shown that PGC-1 could be a promising target for therapies targeting neuromuscular diseases. Among these, some evidence has shown that various signaling pathways linked to PGC-1α are deregulated in muscular dystrophy, leading to a reduced capacity for mitochondrial oxidative phosphorylation and increased reactive oxygen species (ROS) production. In the light of these results, any intervention aimed at activating PGC-1 could contribute towards ameliorating the progression of muscular dystrophies. PGC-1α is influenced by different patho-physiological/pharmacological stimuli. Natural products have been reported to display modulatory effects on PPARγ activation with fewer side effects in comparison to synthetic drugs. Taken together, this review summarizes the current knowledge on Duchenne muscular dystrophy, focusing on the potential effects of natural compounds, acting as regulators of PGC-1α. Elsevier 2020-05 2020-01-08 /pmc/articles/PMC7276681/ /pubmed/32528825 http://dx.doi.org/10.1016/j.apsb.2020.01.001 Text en © 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Suntar, Ipek
Sureda, Antoni
Belwal, Tarun
Sanches Silva, Ana
Vacca, Rosa Anna
Tewari, Devesh
Sobarzo-Sánchez, Eduardo
Nabavi, Seyed Fazel
Shirooie, Samira
Dehpour, Ahmad Reza
Xu, Suowen
Yousefi, Bahman
Majidinia, Maryam
Daglia, Maria
D'Antona, Giuseppe
Nabavi, Seyed Mohammad
Natural products, PGC-1α, and Duchenne muscular dystrophy
title Natural products, PGC-1α, and Duchenne muscular dystrophy
title_full Natural products, PGC-1α, and Duchenne muscular dystrophy
title_fullStr Natural products, PGC-1α, and Duchenne muscular dystrophy
title_full_unstemmed Natural products, PGC-1α, and Duchenne muscular dystrophy
title_short Natural products, PGC-1α, and Duchenne muscular dystrophy
title_sort natural products, pgc-1α, and duchenne muscular dystrophy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276681/
https://www.ncbi.nlm.nih.gov/pubmed/32528825
http://dx.doi.org/10.1016/j.apsb.2020.01.001
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