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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 270 (1971), S. 289-309 
    ISSN: 1432-1912
    Keywords: Amine Uptake Mechanisms ; Catecholamines ; Extraneuronal Binding ; Blood Flow ; Protriptyline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The retention of total radioactivity or3H-noradrenaline (3]H-NA) and in some experiments also its metabolites after administration of (±)-3H-NA was studied in rat hearts and salivary glandsin vitro andin vivo. Intact, atrophied and postganglionically sympathectomized (chronically denervated) glands were used. Protriptyline was administered to interfere with the neuronal amine uptake mechanism. In order to study the possible influence of amine catabolizing enzymes,3H-metaraminol was also used as substratein vitro. At a low3H-NA concentration about equal amounts of radioactivity were retained by intact and atrophied salivary gland slices and by heart slicesin vitro, while in the denervated gland smaller amounts were recovered. By increasing the3H-NA concentration significantly lower amounts of radioactive material were retained in the atrophied than in the intact salivary gland slices, indicating a reduced extraneuronal binding in the atrophied gland tissue.In vitro administration of protriptyline in different concentrations inhibited the retention of radioactivity in heart and atrophied salivary gland slices to about the same extent, while in intact salivary gland slices the effect of the drug was much less pronounced. The difference persisted after using maximally effectives protriptyline concentrations, and was attributed to the high level of NA catabolites, especially normetanephrine (NM), found in the intact glands after protriptyline. When this drug was administeredin vivo in low doses the effect was less pronounced in the atrophied gland slices than in the intact ones. As this difference disappeared when higher doses of protriptyline was administered, it was interpreted as a result of an unequal distribution of the drug by the blood flow. Maximally effective doses of protriptyline exerted at greater effect on the accumulation of total radioactivityin vivo in hearts than in salivary glands.3H-NA, however, was reduced to about the same low level in hearts as in intact salivary glands. A high amount of8H-NM in the intact glands explains this difference. Certain differences in the dose-response relationship for protriptyline between the different organs were observed, which might be attributed to differences in blood flow. Also when3H-metaraminol was used as substrate, protriptyline, when given bothin vitro andin vivo, reduced the amine retention to a greater extent in atrophied salivary gland slices than in intact ones. Since in this case an influence of monoamine oxidase and catechol-O-methyl transferase can be excluded the data point to the importance of a parenchymal uptake mechanism for amine retention.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 21-35 
    ISSN: 1432-1912
    Keywords: Adrenergic Receptors ; Catecholamines ; Extraneuronal Uptake ; Phenoxybenzamine ; β-Receptor Blocking Agents ; Salivary Glands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of an α-receptor blocking agent, phenoxybenzamine, and a series of β-receptor blocking agents on extraneuronal uptake and retention of radioactivity after incubation of rat salivary gland slices with 3H-noradrenaline or 3H-isoprenaline has been investigated. In some experiments with 3H-noradrenaline as substrate, neuronal uptake was prevented by adding protriptyline to the incubation medium. Phenoxybenzamine reduced extraneuronal accumulation of radioactivity after both 3H-noradrenaline and 3H-isoprenaline in a concentration-dependent manner, whereas after propranolol the levels of extraneuronally retained radioactive material were markedly increased, the efflux from the slices not being diminished. Some other nonselective and selective β-receptor blocking agents with and without intrinsic activity were found to produce the same effect as propranolol upon the retention of radioactivity after incubation with 3H-noradrenaline and 3H-isoprenaline. When both phenoxybenzamine and propranolol were present in the incubation medium the effect of extraneuronally retained radioactivity after 3H-noradrenaline as well as after 3H-isoprenaline was the same as when only phenoxybenzamine was used. The metabolic pattern of the radioactivity in the slices revealed that the extraneuronally retained radioactive compounds consisted mainly of tritiated catabolites, especially 3-O-methylated ones. The relationship between the extraneuronal accumulation and adrenergic receptor mechanisms is discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 341 (1990), S. 215-220 
    ISSN: 1432-1912
    Keywords: (±)-Sotalol ; (+)-Sotalol ; (−)-Sotalol ; Monophasic action potential duration ; β-Adrenoceptor affinity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The racemate (±) and the two enantiomers of sotalol were studied with regard to the effects on cardiac repolarization. In addition, the affinity to cardiac β-adrenoceptors was investigated for the enantiomers. The effect on left ventricular monophasic action potential duration was assessed in the isolated perfused guinea-pig heart and the β-adrenoceptor affinity of the compounds was studied, using α1- radioligand binding technique, in cellular membranes prepared from the left ventricular free wall of the cat. Moreover, the β-adrenoceptor blocking potency of (+)-sotalol was studied in isolated strips of guinea-pig papillary muscles. Both the racemate and the two enantiomers of sotalol caused α1- concentration-dependent prolongation of the ventricular monophasic action potential duration. The maximal effect and the concentration causing half maximal effect (EC50 = 13 μmol/l) were similar for the racemate and the enantiomers, indicating lack of stereoselectivity for this effect. The β-adrenoceptor affinity (equilibrium dissociation constant) of (+)-sotalol was 11 μmol/l and 4 μmol/l as estimated by the binding technique and in the isolated muscle strips, respectively. The affinity for (−)-sotalol, estimated by binding, was 0.6 μmol/l. Thus, at concentrations of (+)-sotalol required for α1- significant prolongation of cardiac repolarization, this isomer may cause significant β-blockade. In this study the enantiomeric purity was better than 98%, so that the degree of β-blockade may be even more pronounced if the enantiomeric purity of the (+)-enantiomer is less than 98%.
    Type of Medium: Electronic Resource
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