Skeletal muscle metabolism, contraction force and glycogen utilization during prolonged electrical stimulation in humans. 1986

E Hultman, and L L Spriet

Muscle metabolism and contraction force were examined in the quadriceps femoris muscles of seven volunteers during 45 min of electrical stimulation. Intermittent stimulation was used, with tetanic trains at 20 Hz lasting 1.6 s, separated by pauses of 1.6 s. Muscle biopsies were taken at rest and during stimulation (80 s, 15, 30 and 45 min). During the initial 80 s of stimulation contraction force decreased to 72% of initial force. The glycogenolytic rate was 40.9 mmol glucosyl units kg-1 dry muscle min-1 and glycolytic intermediate levels increased several fold. Muscle phosphocreatine decreased to 26% of resting concentration and the ATP turnover rate from anaerobic sources was 4.99 mmol kg-1 dry muscle s-1. With continued stimulation from 80 s to 15 min, force decreased to 43% of the initial value at 5 min and 31% at 15 min. Glycogenolysis fell to 5.4 mmol kg-1 dry muscle min-1 and glycolytic intermediate levels decreased suggesting that anaerobic glycolysis contributed progressively less ATP for force production. The final 30 min of stimulation was characterized by a low rate of glycogenolysis (1.35-1.67 mmol kg-1 dry muscle min-1) and a constant force production (25.5% of initial). The ATP turnover rate, assuming glycogen was metabolized aerobically, was 1.86 mmol kg-1 dry muscle s-1. Phosphocreatine, ATP and glycolytic intermediates returned to near resting levels, indicating that anaerobic energy pathways were not reactivated.(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D007537 Isometric Contraction Muscular contractions characterized by increase in tension without change in length. Contraction, Isometric,Contractions, Isometric,Isometric Contractions
D008297 Male Males
D009119 Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. Inotropism,Muscular Contraction,Contraction, Muscle,Contraction, Muscular,Contractions, Muscle,Contractions, Muscular,Inotropisms,Muscle Contractions,Muscular Contractions
D009132 Muscles Contractile tissue that produces movement in animals. Muscle Tissue,Muscle,Muscle Tissues,Tissue, Muscle,Tissues, Muscle
D010725 Phosphocreatine An endogenous substance found mainly in skeletal muscle of vertebrates. It has been tried in the treatment of cardiac disorders and has been added to cardioplegic solutions. (Reynolds JEF(Ed): Martindale: The Extra Pharmacopoeia (electronic version). Micromedex, Inc, Englewood, CO, 1996) Creatine Phosphate,Neoton,Phosphocreatine, Disodium Salt,Phosphorylcreatine,Disodium Salt Phosphocreatine,Phosphate, Creatine
D004558 Electric Stimulation Use of electric potential or currents to elicit biological responses. Stimulation, Electric,Electrical Stimulation,Electric Stimulations,Electrical Stimulations,Stimulation, Electrical,Stimulations, Electric,Stimulations, Electrical
D005260 Female Females
D006003 Glycogen
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000255 Adenosine Triphosphate An adenine nucleotide containing three phosphate groups esterified to the sugar moiety. In addition to its crucial roles in metabolism adenosine triphosphate is a neurotransmitter. ATP,Adenosine Triphosphate, Calcium Salt,Adenosine Triphosphate, Chromium Salt,Adenosine Triphosphate, Magnesium Salt,Adenosine Triphosphate, Manganese Salt,Adenylpyrophosphate,CaATP,CrATP,Manganese Adenosine Triphosphate,MgATP,MnATP,ATP-MgCl2,Adenosine Triphosphate, Chromium Ammonium Salt,Adenosine Triphosphate, Magnesium Chloride,Atriphos,Chromium Adenosine Triphosphate,Cr(H2O)4 ATP,Magnesium Adenosine Triphosphate,Striadyne,ATP MgCl2

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