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  • 1970-1974  (2)
  • Extraneuronal O-Methylation  (1)
  • Perfused Rabbit Hearts  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 191-218 
    ISSN: 1432-1912
    Keywords: Isoprenaline ; Extraneuronal Uptake ; Extraneuronal O-Methylation ; Rat Heart ; Removal of Isoprenaline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Isolated rat and guinea-pig hearts were perfused with 0.95 μM (±)-isoprenaline or 3H(±)-isoprenaline, a catecholamine which is taken up by extraneuronal mechanisms only. From measurements of the arterio-nevous difference (by fluorimetry and by scintillation counting, respectively) the rate of removal of the amine from the perfusion fluid was measured; in addition, the rate of appearance of its metabolite (3-O-methyl-3H-isoprenaline; 3H-OMI) was determined in the venous effluent as well as the accumulation of 3H-isoprenaline and 3H-OMI in the heart. 2. Experiments with sodium thiocyanate and 14C-sorbitol showed that these agents distributed into the extracellular space (about 350 μl/g; t/2 for efflux of about 1.2 min) and into ventricular and atrial cavities (about 1500 μl/g; t/2 for efflux of 0.1 to 0.2 min). 3. The removal of 3H-isoprenaline from the perfusion fluid declined biphasically with time; after an initial rapid decline the rate of removal approached steadystate levels within about 30 min. After block of COMT (by the presence of 100 μM U-0521) the second phase of decline approached zero. In the absence of U-0521 the steady-state rate of removal was 10 times higher in rat than in guinea-pig hearts; in the presence of U-0521 the approach to zero was faster for guinea-pig than for rat hearts. 4. When COMT was intact, 3H-OMI appeared in the venous effluent, first at a rapidly increasing rate, from the 9th minute of perfusion onward at a steady rate which was identical with the steady-state rate of removal of 3H-isoprenaline. No 3H-OMI was detected after block of COMT. 5. The accumulation of 3H-isoprenaline in the heart reached a steady level within about 30 min; block of COMT increased the time required for approach to steady levels and increased the accumulation of 3H-isoprenaline in the rat (but not in the guinea-pig) heart. When COMT was intact, the accumulation of 3H-OMI in the heart reached steady-state levels within 10 min. 6. The time-dependent decline of the rate of removal of 3H-isoprenaline by hearts whose COMT had been inhibited was due to a time-dependent increase of the rate of efflux of the amine from the stores; there did not seem to be any change in the rate of gross influx. 7. Isoprenaline-induced ventricular fibrillation reduced the rate of O-methylation of 3H-isoprenaline significantly. 8. Perfusion of hearts with 0.095 μM (±)-isoprenaline resulted in a significantly greater accumulation of the amine in rat than in guinea-pig and rabbit hearts.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 271 (1971), S. 1-28 
    ISSN: 1432-1912
    Keywords: Noradrenaline Uptake ; Block of Monoamine Oxidase ; Reserpine ; Axoplasmic Noradrenaline ; Perfused Rabbit Hearts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Isolated rabbit hearts were perfused with 20 to 200 ng/ml of (−)-noradrenaline and arterio-venous differences were determined at various times to measure the rate of net removal of the amine from the perfusion fluid. Animals were untreated or pretreated with reserpine and/or pargyline to block vesicular retention and/or intraneuronal monoamine oxidase (MAO). The arterio-venous difference (in percent of the arterial concentration) remained rather constant during prolonged perfusions of untreated hearts with (−)-noradrenaline, the magnitude of the difference being inversely related to the arterial concentration. After block of MAO the rate of net removal declined exponentially with time; the rate of decline increased with increasing arterial concentration of the amine and also after the additional pretreatment with reserpine. The time-dependent decline in the rate of net removal was shown to be due to an increased efflux of the amine from the nerve endings. The net removal of noradrenaline-H3 at the 5th min of perfusion of pargyline-pretreated hearts was mainly due to neuronal net uptake, since a) O-methylation accounted for only 5% of the removal, and b) cocaine (10–30 (μg/ml) virtually abolished net removal. Initial rates of removal were not affected by the various pretreatments. In untreated hearts retention of exogenous (−)-noradrenaline increased linearly with the duration of the perfusion but the increase was exponential after block of MAO. Apparently, the storage capacity becomes exhausted during prolonged perfusions of pargyline-pretreated hearts. The ratio “noradrenaline retained by the heart/noradrenaline removed by the heart” was quite small in untreated (0.16), very small in reserpine-pretreated (0.03) and nearly unity in pargyline-pretreated hearts. It is concluded that any impairment of the intraneuronal mechanisms of inactivation (vesicular storage and MAO) leads to an increase in the axoplasmic concentration of free noradrenaline which causes an increased efflux of the amine, while the influx remains unchanged. The axoplasmic concentration of free noradrenaline seems to rise more after block of MAO than after pretreatment with reserpine and is most pronounced after both. Changes in the sensitivity of the pacemaker to (−)-noradrenaline were found to be correlated with changes in the rate of removal of the amine from the perfusion fluid.
    Type of Medium: Electronic Resource
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