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  • Analytical Chemistry and Spectroscopy  (3)
  • Glycogen  (1)
  • 1980-1984  (3)
  • 1965-1969  (1)
Document type
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 389 (1981), S. 277-282 
    ISSN: 1432-2013
    Keywords: Lactate ; Glycogenolysis ; Muscle contraction ; Glycogen ; Human muscle ; Recovery
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Isometric contraction of the quadriceps muscle sustained to fatigue with a force of 66% of the maximum voluntary contraction force resulted in a mean glycogen utilization of 80.4 (S.D. 58.4) mmol glucosyl units/kg dry muscle (d.m.) and an accumulation of glycolytic intermediates and glucose corresponding to 82.9 (S.D. 17.5) mmol glucosyl units/kg d.m. Accumulation of hexose phosphates (principally glucose 6-phosphate) accounted for 35.4% (S.D. 4.1) of the total increase and lactate for 59.3% (S.D. 2.8). During a 4 min recovery period glucose 6-[hosphate content showed a linear decrease with a half time of 2.0 min and lactate decreased exponentially with a half time of 2.5 min. The rate of lactate disappearance from the muscle was approximately 4 times as fast as that observed previously after maximal bicycle exercise. This was probably due to a lower lactate concentration in blood after isometric contraction resulting in a larger muscle-blood gradient for lactate. Muscle content of free glucose was increased after contraction and increased further during recovery. It is concluded that the glucose increase is confined to the intracellular pool and is an effect of hexokinase inhibition by accumulated glucose 6-phosphate. Occlusion, of the local circulation after the contraction inhibited the recovery processes for lactate and glucose 6-phosphate.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 22 (1984), S. 784-788 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-resolution 13C NMR spectra of solid 1,4-bis(n-butylamino)anthraquinone are presented. In spectra measured at 22.6 MHz the effects of two short-range and two long-range residual (13C, 14N) dipolar couplings have been observed. Only the short-range effects are observable in the 50.3 MHz spectra. These typical asymmetric doublets allow the determination of the 14N nuclear quadrupole coupling constant (χ=e2Qq/h=-3.0 MHz), the asymmetry parameter (η=0.3) and the orientation of the electric field gradient tensor of the 14N in the molecular framework.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 1 (1969), S. 329-335 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proton magnetic resonance spectra of methylene dichloride solutions containing N-methyl morpholine and sulphur dioxide have been studied as a function of temperature. Complex formation reduces the rate of interchange of magnetic sites via inversion at nitrogen but increases the rate of ring inversion. The conformational preference of the complex is discussed. It is suggested that interaction with SO2 may be a useful general method of studying nitrogen inversion.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 21 (1983), S. 464-464 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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