Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications

Peroxisome proliferator-activated receptor β/δ (PPARβ/δ) has emerged as a powerful metabolic regulator in diverse tissues including fat, skeletal muscle, and the heart. It is now established that activation of PPARβ/δ promotes fatty acid oxidation in several tissues, such as skeletal muscle...

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Main Author: Adnan Erol
Format: Article
Language:English
Published: Hindawi Limited 2007-01-01
Series:PPAR Research
Online Access:http://dx.doi.org/10.1155/2007/30578
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spelling doaj-36f1094684f84d96ba87c336a1e4fa172020-11-25T01:03:23ZengHindawi LimitedPPAR Research1687-47571687-47652007-01-01200710.1155/2007/3057830578Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style ModificationsAdnan Erol0Department of Internal Medicine, Faculty of Medicine, Celal Bayar University, Manisa 45040, TurkeyPeroxisome proliferator-activated receptor β/δ (PPARβ/δ) has emerged as a powerful metabolic regulator in diverse tissues including fat, skeletal muscle, and the heart. It is now established that activation of PPARβ/δ promotes fatty acid oxidation in several tissues, such as skeletal muscle and adipose tissue. In muscle, PPARβ/δ appears to act as a central regulator of fatty acid catabolism. PPARβ/δ contents are increased in muscle during physiological situations such as physical exercise or long-term fasting, characterized by increased fatty acid oxidation. Targeted expression of an activated form of PPARβ/δ in skeletal muscle induces a switch to form increased numbers of type I muscle fibers resembling the fiber type transition by endurance training. Activation of PPARβ/δ also enhances mitochondrial capacity and fat oxidation in the skeletal muscle that resembles the effect of regular exercise. Therefore, it is hypothesized that muscle-specific PPARβ/δ agonists could be a key strategy to support the poor cardiorespiratory fitness associated with metabolic disorders.http://dx.doi.org/10.1155/2007/30578
collection DOAJ
language English
format Article
sources DOAJ
author Adnan Erol
spellingShingle Adnan Erol
Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications
PPAR Research
author_facet Adnan Erol
author_sort Adnan Erol
title Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications
title_short Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications
title_full Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications
title_fullStr Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications
title_full_unstemmed Muscle-Specific PPARβ/δ Agonism May Provide Synergistic Benefits with Life Style Modifications
title_sort muscle-specific pparβ/δ agonism may provide synergistic benefits with life style modifications
publisher Hindawi Limited
series PPAR Research
issn 1687-4757
1687-4765
publishDate 2007-01-01
description Peroxisome proliferator-activated receptor β/δ (PPARβ/δ) has emerged as a powerful metabolic regulator in diverse tissues including fat, skeletal muscle, and the heart. It is now established that activation of PPARβ/δ promotes fatty acid oxidation in several tissues, such as skeletal muscle and adipose tissue. In muscle, PPARβ/δ appears to act as a central regulator of fatty acid catabolism. PPARβ/δ contents are increased in muscle during physiological situations such as physical exercise or long-term fasting, characterized by increased fatty acid oxidation. Targeted expression of an activated form of PPARβ/δ in skeletal muscle induces a switch to form increased numbers of type I muscle fibers resembling the fiber type transition by endurance training. Activation of PPARβ/δ also enhances mitochondrial capacity and fat oxidation in the skeletal muscle that resembles the effect of regular exercise. Therefore, it is hypothesized that muscle-specific PPARβ/δ agonists could be a key strategy to support the poor cardiorespiratory fitness associated with metabolic disorders.
url http://dx.doi.org/10.1155/2007/30578
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