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Chapter 6. muscular mechanism in aerobic endurance training. PF. Gardiner, Advanced neuromuscular exercise physiology. Limitations of techniques. Muscle biopsy Combination of fiber types Representative of entire muscle? Chronic electric stimulation Non-voluntary
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Chapter 6. muscular mechanism in aerobic endurance training PF. Gardiner, Advanced neuromuscular exercise physiology
Limitations of techniques • Muscle biopsy • Combination of fiber types • Representative of entire muscle? • Chronic electric stimulation • Non-voluntary • Unreachable training volume/intensity
Coordination of muscle protein systems • The coordinated expression of many proteins simultaneously • common transcription factors and metabolic signals that promote the expression of several genes • Changes in type 1 fibers,including heavy chains, light chains, and thin filament proteins
Pre-translational control • Changes in mRNA abundance • Transcription rate, mRNA processing, mRNA stability • Can happen after several contractions, up to several hours after exercise • In chronically stimulated muscles, mRNA levels generally reflect protein levels • Mitochondrial mRNA/DNA ratio remain unchanged • Mitochondria proliferation ↑DNA
Hypoxic training • Hypoxia alone has a unique stimulatory effect • expression of several genes associated with improved metabolism and performance. • Induction of hypoxia-inducible factor-1 (HIF-1) • involved in upregulatingthe expression of proteins involved in glycolysis, pH regulation, and angiogenesis
Translational control • Initiation, elongation, termination • Receptor-binding and mitogen-activated protein kinase (MAPK) signaling systems • ↑ribosomal RNA 7X in first 2 weeks of stimulation in rabbit muscles • Enhanced translational efficiency • Translation may be altered in order to coordinate the expression of two proteins whose functions are closely linked
Time course of changes in mRNA and protein concentration SERCA: sarco/endop1asmic reticu1um calcium.ATPase
Posttranslational modifications • Phosphorylation, subunit assembly, transport, degradation • Protein synthesis rate < its incorporation into fiber as functional component
Posttranslational modifications • Ubiquitin proteasome system • Principal protein degradation mechanism in muscle fibers • ↑protein stability • ↑protein concentration without ↑mRNA
Adaptations can occur ex vivo • adaptations to chronic electrical stimulation can be reproduced quite closely in denervatedmuscles and in culture • Do NOT require intact innervation • Do NOT require voluntarily contraction
Metabolic signals and adaptation • Metabolic signaling • ATP/ADP • AMP-activated kinase (AMPK) • PPARs: free fatty acids • Ca2+ signaling • ↑intracellular Ca after days of electric stimulation • Calcineurin; calcium-regulated phosphatase • Ionophore A23187
Metabolic signals and adaptation • Mechanical signaling • Activation of MAPK signaling pathways, activated by several types of stresses • JNK family: stress-activated protein kinases • Hormones, autocrine or paracrine factors • Insulin-like growth factor 1 (IGF-1) • Hypoxia, H+, reactive-oxygen species
Hormone nuclear receptors Ex Biochem c8-signal transduction
25.7 Response Elements Are Recognized by Activators • Response elements may be located in promoters or enhancers. Figure 25.11 Ex Biochem c8-signal transduction
Class II hormone nuclear receptor Ex Biochem c8-signal transduction
粒線體生合成的基因調控機制 Reznick et al, 2006
Proposed mechanism Ex Biochem c8-signal transduction PGC1a: peroxisome proliferator-activated receptor coactivator-1alpha
WT: wild type TG: transgenic, expression of an activated form of PPARdelta in skeletal muscle GW501516, GW1516PPARdelta agonist Wang YX, PLOSB 2004