Abstract
The expression of two isoforms of insulin-like growth factor-I (IGF-I): mechano growth factor (MGF) and IGF-IEa were studied in muscle in response to growth hormone (GH) administration with and without resistance training in healthy elderly men. A third isoform, IGF-IEb was also investigated in response to resistance training only. The subjects (age 74 +/- 1 years, mean +/- S.E.M) were assigned to either resistance training with placebo, resistance training combined with GH administration or GH administration alone. Real-time quantitative RT-PCR was used to determine mRNA levels in biopsies from the vastus lateralis muscle at baseline, after 5 and 12 weeks in the three groups. GH administration did not change MGF mRNA at 5 weeks, but significantly increased IGF-IEa mRNA (237%). After 12 weeks, MGF mRNA was significantly increased (80%) compared to baseline. Five weeks of resistance training significantly increased the mRNA expression of MGF (163%), IGF-IEa (68%) and IGF-IEb (75%). No further changes were observed after 12 weeks. However, after 5 weeks of training combined with GH treatment, MGF mRNA increased significantly (456%) and IGF-IEa mRNA by (167%). No further significant changes were noted at 12 weeks. The data suggest that when mechanical loading in the form of resistance training is combined with GH, MGF mRNA levels are enhanced. This may reflect an overall up-regulation of transcription of the IGF-I gene prior to splicing.
Original language | English |
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Journal | The Journal of Physiology |
Volume | 555 |
Issue number | Pt 1 |
Pages (from-to) | 231-40 |
Number of pages | 10 |
ISSN | 0022-3751 |
DOIs | |
Publication status | Published - 15 Feb 2004 |
Keywords
- Aged
- Aged, 80 and over
- Aging/drug effects
- Analysis of Variance
- Double-Blind Method
- Exercise/physiology
- Gene Expression Regulation/drug effects
- Human Growth Hormone/pharmacology
- Humans
- Insulin-Like Growth Factor I/biosynthesis
- Male
- Muscle, Skeletal/drug effects
- Protein Isoforms/biosynthesis
- RNA, Messenger/biosynthesis
- Recombinant Proteins/pharmacology
- Weight Lifting/physiology