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Expression of IGF-I splice variants in young and old human skeletal muscle after high resistance exercise
Open accessAbstract
The mRNA expression of two splice variants of the insulin-like growth factor-I (IGF-I) gene, IGF-IEa and mechano growth factor (MGF), were studied in human skeletal muscle. Subjects (eight young, aged 25-36 years, and seven elderly, aged 70-82 years) completed 10 sets of six repetitions of single legged knee extensor exercise at 80 % of their one repetition maximum. Muscle biopsy samples were obtained from the quadriceps muscle of both the control and exercised legs 2.5 h after completion of the exercise bout. Expression levels of the IGF-I mRNA transcripts were determined using real-time quantitative RT-PCR with specific primers. The resting levels of MGF were significantly (approximately 100-fold) lower than those of the IGF-IEa isoform. No difference was observed between the resting levels of the two isoforms between the two subject groups. High resistance exercise resulted in a significant increase in MGF mRNA in the young, but not in the elderly subjects. No changes in IGF-IEa mRNA levels were observed as a result of exercise in either group. The mRNA levels of the transcription factor MyoD were greater at rest in the older subjects (P < 0.05), but there was no significant effect of the exercise bout. Electrophoretic separation of myosin heavy chain (MHC) isoforms showed the older subjects to have a lower (P < 0.05) percentage of MHC-II isoforms than the young subjects. However, no association was observed between the composition of the muscle and changes in the IGF-I isoforms with exercise. The data from this study show an attenuated MGF response to high resistance exercise in the older subjects, indicative of age-related desensitivity to mechanical loading. The data in young subjects indicate that the MGF and IGF-IEa isoforms are differentially regulated in human skeletal muscle.
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“The hypertrophic response to strength training exercise has been reported to be greater in type II fibres which express the MHC-IIa and IIX isoforms (Tesch et al. 1985; Kadi et al. 1999; Aagaard et al. 2001; Andersen & Aagaard, 2000).”
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Metadata
- Authors
- Hameed, M., Orrell, R. W., COBBOLD, M., Goldspink, G., & Harridge, S. D. R.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2002-12-20
- Volume
- 547
- Issue
- 1
- Pages
- 247-254
- ISSN
- 0022-3751 (ISSN-L)
- OpenAlex
- W2156148379
- Cited by
- 416
- References
- 3
- FWCI
- 7.02
- Type
- journal article
- Language
- en
- Open access
- green
- Licence
- doi.wiley.com/10.1002/tdm_license_1 (tdm, 4638 d)
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