Literature DB >> 9790915

Exercise stimulates c-Jun NH2 kinase activity and c-Jun transcriptional activity in human skeletal muscle.

D Aronson1, M D Boppart, S D Dufresne, R A Fielding, L J Goodyear.   

Abstract

Exercise causes selective changes in gene expression leading to alterations in the structure and function of human skeletal muscle. However, little is known about the specific signaling pathways that enable exercise to modulate gene regulatory events. We determined the effects of exercise on c-Jun NH2-terminal kinase (JNK) activity, a signaling molecule involved in the regulation of transcription. Biopsies of vastus lateralis muscle were taken from eight subjects at rest and after 60 min of cycle ergometer exercise. Exercise increased JNK activity in all subjects (5.9 +/- 1.8 fold above basal). JNK activation was associated with an increased expression of its downstream nuclear target c-Jun mRNA. When two additional subjects were studied using a one-legged exercise protocol, JNK activity increased only in the exercising leg, indicating that exercise-induced JNK signaling represents an intrinsic response of the contracting muscle, rather than a systemic response to exercise. These studies demonstrate that the JNK pathway may serve as a link between contractile activity and transcriptional responses in human skeletal muscle. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9790915     DOI: 10.1006/bbrc.1998.9435

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  24 in total

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Review 5.  PGC-1alpha regulation by exercise training and its influences on muscle function and insulin sensitivity.

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7.  Marathon running transiently increases c-Jun NH2-terminal kinase and p38 activities in human skeletal muscle.

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8.  Contraction-induced interleukin-6 gene transcription in skeletal muscle is regulated by c-Jun terminal kinase/activator protein-1.

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Journal:  J Sports Sci Med       Date:  2002-12-01       Impact factor: 2.988

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