» Articles » PMID: 14633846

Endurance Training in Humans Leads to Fiber Type-specific Increases in Levels of Peroxisome Proliferator-activated Receptor-gamma Coactivator-1 and Peroxisome Proliferator-activated Receptor-alpha in Skeletal Muscle

Overview
Journal Diabetes
Specialty Endocrinology
Date 2003 Nov 25
PMID 14633846
Citations 188
Authors
Affiliations
Soon will be listed here.
Abstract

The peroxisome proliferator-activated receptor (PPAR)-gamma coactivator-1 (PGC-1) can induce mitochondria biogenesis and has been implicated in the development of oxidative type I muscle fibers. The PPAR isoforms alpha, beta/delta, and gamma control the transcription of genes involved in fatty acid and glucose metabolism. As endurance training increases skeletal muscle mitochondria and type I fiber content and fatty acid oxidative capacity, our aim was to determine whether these increases could be mediated by possible effects on PGC-1 or PPAR-alpha, -beta/delta, and -gamma. Seven healthy men performed 6 weeks of endurance training and the expression levels of PGC-1 and PPAR-alpha, -beta/delta, and -gamma mRNA as well as the fiber type distribution of the PGC-1 and PPAR-alpha proteins were measured in biopsies from their vastus lateralis muscle. PGC-1 and PPAR-alpha mRNA expression increased by 2.7- and 2.2-fold (P < 0.01), respectively, after endurance training. PGC-1 expression was 2.2- and 6-fold greater in the type IIa than in the type I and IIx fibers, respectively. It increased by 2.8-fold in the type IIa fibers and by 1.5-fold in both the type I and IIx fibers after endurance training (P < 0.015). PPAR-alpha was 1.9-fold greater in type I than in the II fibers and increased by 3.0-fold and 1.5-fold in these respective fibers after endurance training (P < 0.001). The increases in PGC-1 and PPAR-alpha levels reported in this study may play an important role in the changes in muscle mitochondria content, oxidative phenotype, and sensitivity to insulin known to be induced by endurance training.

Citing Articles

Skeletal muscle atrophy and dysfunction in obesity and type-2 diabetes mellitus: Myocellular mechanisms involved.

Castillo I, Argiles J, Rueda R, Ramirez M, Pedrosa J Rev Endocr Metab Disord. 2025; .

PMID: 40064750 DOI: 10.1007/s11154-025-09954-9.


Role of the Gene and Its rs8192678 Polymorphism on Sport Performance, Aerobic Capacity, Muscle Adaptation and Metabolic Diseases: A Narrative Review.

Varillas-Delgado D Genes (Basel). 2025; 15(12.

PMID: 39766897 PMC: 11675316. DOI: 10.3390/genes15121631.


Impact of exercise and fasting on mitochondrial regulators in human muscle.

Menezes E, Islam H, Arhen B, Simpson C, McGlory C, Gurd B Transl Exerc Biomed. 2024; 1(3-4):183-194.

PMID: 39703531 PMC: 11653475. DOI: 10.1515/teb-2024-0014.


The muscle-intervertebral disc interaction mediated by L-BAIBA modulates extracellular matrix homeostasis and PANoptosis in nucleus pulposus cells.

Qin T, Shi M, Zhang C, Wu J, Huang Z, Zhang X Exp Mol Med. 2024; 56(11):2503-2518.

PMID: 39511429 PMC: 11612187. DOI: 10.1038/s12276-024-01345-5.


Relationships between endurance exercise training-induced muscle fiber-type shifting and autophagy in slow- and fast-twitch skeletal muscles of mice.

Kwon I, Kim K, Lee Y Phys Act Nutr. 2024; 28(2):23-34.

PMID: 39097995 PMC: 11298286. DOI: 10.20463/pan.2024.0013.