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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 398 (1983), S. 210-216 
    ISSN: 1432-2013
    Keywords: Caffeine ; Ca2+-activated force ; Skinned muscle fibres ; Cardiac muscle ; Skeletal muscle ; Theophylline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Skinned fibres prepared by mechanical and/or chemical means from cardiac and skeletal muscles of the rat were activated in solution strongly buffered for Ca2+ (with 50 mM EGTA) in the absence or presence of caffeine 5–40 mM. In all preparations caffeine was found to reversibly shift the relation between steady-state force and free [Ca2+] toward lower free [Ca2+] in a dose dependent manner. This increase in apparent Ca2+ sensitivity was not antagonized by procaine and was the same, within each muscle type, irrespective of the manner in which the skinned fibre was prepared, and consequently the degree to which it retained cellular membranes. The effect was more pronounced in cardiac and slow-twitch than in fast-twitch, myofibrillar preparations. At equivalent concentrations theophylline mimicked this effect of caffeine in all preparations, however, addition of exogenous cyclic AMP neither mimicked nor modified, in any way, the effect. Maximum Ca2+-activated force production was not affected by caffeine below 20 mM but was depressed by concentrations of 20 mM and above. The increase in apparent Ca2+ sensitivity produced by caffeine can not be the result of a mobilization of some cellular store of Ca2+ but must arise from a direct effect of caffeine on the myofilaments which leads to a change in the apparent affinity constant of the force controlling sites for Ca2+.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 831-832 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H NMR spectra of 1,3-benzodithiole and eight derivatives have been analysed. Signals of the protons in positions 4 and 7 are shifted downfield compared with those for the protons in positions 5 and 6. The inter-ring proton-proton couplings have been determined.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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