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  • 1
    ISSN: 1432-2013
    Keywords: Skeletal muscle ; Hyperthyroidism ; Fibre types ; 86Rb influx
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The influence of experimental hyperthyroidism on the catecholamine induced stimulation of rubidium ion transport in the soleus (SOL), a slow-twitch muscle and the extensor digitorum longus (EDL), a fast-twitch skeletal muscle of rats was studied. Thyroxine administration (800 μg/kg/day), for ten days induced a rise of ouabainsensitive86Rb uptake in SOL muscle, without affecting the ouabain-insensitive uptake, whereas both fractions of86Rb uptake were increased in EDL muscle from hyperthyroid rats. Isoproterenol (5 μmol/l) caused a two-fold rise in ouabain-sensitive Rb uptake of euthyroid SOL muscle, while in hyperthyroid SOL it could stimulate only the ouabain-insensitive fraction of86Rb influx. On the other hand, the stimulating action of isoproterenol on euthyroid EDL muscle was due to an enhancement of ouabain-insensitive Rb uptake, but in hyperthyroid EDL it failed to stimulate the ouabain-insensitive transport and caused a marked rise in ouabain-sensitive Rb uptake. The changes in catecholamine mediated transport properties in SOL muscle may be related to fibre type trans-formation induced by thyroid hormone, although in EDL the changes of catecholamine stimulation are unlikely due to fibre type conversion. Basal and isoproterenol stimulated cAMP levels were significantly reduced in both EDL and SOL muscles from hyperthyroid rats, in contrast with an insignificant decrease in net rubidium uptake caused by isoproterenol at the same concentration.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0947-3440
    Keywords: Gloeophyllum abietinum ; Oosponol ; Isocoumarin ; Structure-activity relationships ; Antibiotics ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The toxic metabolite of the basidiomycete Gloeophyllum abietinum, oosponol (6b), and the structural analogues (Figure 1) were synthesised in order to investigate which partial structures of the molecules are responsible for their biological activities. Different organisms were employed to test the antibiotic activities of the analogues. From the results obtained with the synthetic analogues of oosponol (6b), it became evident that the toxicity of this fungal metabolite can be attributed to a vinylogous acid anhydride structure, which in nature is produced by dehydrogenation of the nontoxic precursor oospoglycol (7).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0947-3440
    Keywords: Isocoumarin ; Oosponol ; Pseudomonas fluorescens ; Antibiotics ; Secondary fungal metabolite ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The partial synthesis of oosponol (4), which shows significant antibiotic activity, has been accomplished by enzyme catalyzed reactions including regioselective acetylation of (-)-oospoglycol (1) followed by an oxidation step and hydrolysis by a lipase.
    Type of Medium: Electronic Resource
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