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运动对大鼠骨骼肌IGF-Ⅰ、MGF基因表达的影响 被引量:4

Effects of Exercise on The Insulin-like Growth Factor-Ⅰ mRNA、MGF mRNA Expression in Skeletal Muscle of Rats
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摘要 目的探讨三种不同训练方式对大鼠骨骼肌IGF-Ⅰ、MGF基因表达的影响。方法32只SD大鼠随机分为安静组(C),长期训练组(T),负重训练组(O)和一次急性负重运动组(AO),每组8只。T组进行8周每天60 min的游泳运动;O组进行4周每天60 min的负重游泳运动;AO组在处死当天负重游泳60 min。T组和O组末次训练后24 h切取腓肠肌,Real-time PCR检测IGF-Ⅰ Ea和MGF的mRNA表达。结果(1)T组IGF-Ⅰ Ea mRNA表达显著高于C组(P<0.05),O组IGF-Ⅰ Ea mRNA表达显著高于C组(P<0.05),AO组IGF-Ⅰ Ea mRNA表达非常显著地高于C组(P<0.01);(2)T组MGF mRNA表达显著高于C组(P<0.05),O组MGF mRNA表达显著高于C组(P<0.05),AO组MGF mRNA表达极显著地高于C组(P<0.01)。结论负重游泳运动致使IGF-Ⅰ Ea mRNA和MGF mRNA表达升高,骨骼肌产生损伤,同时卫星细胞增殖,骨骼肌细胞进行损伤再修复过程。说明IGF-Ⅰ有刺激卫星细胞增殖,并促进增殖的细胞分化,改善骨骼肌结构,修复损伤肌肉。 Objective To investigate the effects of exercise on the gene expression of IGF- I and MGF. Methods 32 male SD rats were randomly and equally divided into four groups: control group (C), training group (T), overload training group (O) and acute bout overload exercise group (AO). The rats of training group take 8 weeks (60 min/d) swimming exercise; the rats of overload training group take 4 weeks (60 min/d) swimming exercise with overload; the rots of acute bout overload exercise group take 60rain swimming exercise with overload before killed. 24h after the last training, the rats of T group and O group were killed, gastrocnernius was excised quickly for Real - time PCR analysis. Results ( 1 ) The IGF - I Ea mRNA expression was upregulated significantly in T and O ( P 〈 0.05), and was uprcgulated significantly in AO ( P 〈0.01); (2) The MGF mRNA expression was upregulated significantly in T and O ( P 〈 0.05), and was upregulated significantly in AO ( P 〈 0.01 ). Conclusion The expression of skeletal muscle IGF - I Ea and MGF mRNA in overload group and acute bout overload group significantly increased compared with control group, indicated that muscle satellite cell were stimulated and were required for local muscle repair by IGF- I.
出处 《西安体育学院学报》 CSSCI 北大核心 2010年第1期80-83,共4页 Journal of Xi'an Physical Education University
关键词 胰岛素样生长因子-Ⅰ 胰岛素样生长因子-IEa 机械生长因子 肌卫星细胞 骨骼肌 运动 IGF-I IGF-I Ea MGF muscle satellite (stem) cells skeletal muscle exercise
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  • 1Goldspink G, Scutt A, Loughna PT, et al. Gene expression in skeletal muscle in response to stretch and force generation [J].Am J Physiol, 1992, 262(3) : 356-363. 被引量:1
  • 2Yang S Y, Alnaqeeb Majed, Simpson Hamish, et al. Cloning and characterization of an IGF-Ⅰ isoform expressed in skeletal muscle subjected to stretch [ J]. J Muscle Res Cell Motility, 1996, 17(4) : 487-495. 被引量:1
  • 3McKoy G, Ashley W, Mander J, et al. Expression of insulin-like growth factor-Ⅰ splice variant and structural genes in rabbit skeletal muscle induced by stretch and stimulation [ J]. J Physiol, 1999, 516(2): 583-592. 被引量:1
  • 4Ploug T, Stallknecht B M, Pedersen O, et al. Effect of endurance training on glucose transport capacity and glucose transporter expression in rat skeletal muscle [ J]. Am J Physiol Endocrinol Metab, 1990, 259(6): E778-E786. 被引量:1
  • 5Mariana de Rezende Gomes, Ivanir Santana de Oliveira Pires, Inar Alves de Castro, et al. Effect of moderate physical exercise on plasma and tissue levels of insulin-like growth factor-I in adult rats[J]. Nutrition Research, 2004, 24(7): 555-564. 被引量:1
  • 6Brown S C, Stickland N C, Satellite cell content in muscles of large and small mice [J]. J Anat, 1993, 183(1): 91-96. 被引量:1
  • 7Gregory R,Adams, Samuel A,et al. localized infusion of IGF-Ⅰ results in skeletal muscle hypertrophy in rats [ J ]. J Appl Physiol, 1998, 84(5): 1716-1722. 被引量:1
  • 8Humbel R E. Insulin-like growth factor 1 and 2 [ J ]. Eur J Biochem, 1990, 190(3): 445-462. 被引量:1
  • 9Hameed M, Orrell R W, Cobbold M,et al. Expression of IGF-Ⅰ splice variants in young and old human skeletal muscle after high resistance exercise [J]. J Physiol, 2003, 547(1) : 247-254. 被引量:1
  • 10Maria Hill, Geoffrey Goldspink. Expression and splicing of the insulin-like growth factor gene in rodent muscle is associated with muscle satellite (stem) cell activation following local tissue damage [J]. J Physiol, 2003, 549(1): 409-418. 被引量:1

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