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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 38 (1982), S. 844-845 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The inhibition of monoamine oxidase (MAO) activity by d-amphetamine was measured in homogenates of cat superior cervical ganglion and nictitating membrane, using tyramine (TM) and noradrenaline (NA) as substrates. In both tissues, d-amphetamine was shown to be a competitive inhibitor of the oxidation of TM. The Ki for d-amphetamine, as a MAO inhibitor, was lower in the ganglia than in the peripheral nerve endings.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 23 (1967), S. 665-666 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Zusammenfassung Die Autoren stellen fest, dass bei Ratten durch Kastration der Gehalt an Noradrenalin und Dopamin im vordern Teil des Hypothalamus ansteigt. Erst hohe Dosen von Östradiol und Progesteron können den Kastrationseffekt wieder zum Verschwinden bringen.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 299 (1977), S. 225-238 
    ISSN: 1432-1912
    Keywords: Stereoselective metabolism of noradrenaline ; Neuronal efflux ; Cocaine ; Phenoxybenzamine ; Rat vas deferens
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The metabolism of 3H-(-)- and 3H-(±)-noradrenaline (NA) was studied in the isolated rat vas deferens either under conditions of uptake or of efflux of the amine. Any differences obtained between 3H-(-)-and 3H-(±)NA as substrate were interpreted as being a reflection of differences between the two isomers of the amine. 2. Uptake experiments (0.13 μM; 7.5 min) showed that neuronal mechanisms of amine disposition prevail over extraneuronal ones. Thus, most of the metabolites of 3H-NA formed during incubation with the amine (including the O-methylated products) were of neuronal origin. The acid deaminated metabolite 3,4-dihydroxymandelic acid (DOMA), tended to be much better retained by the tissue than the neutral deaminated metabolite, 3,4-dihydroxyphenylethyleneglycol (DOPEG). While neuronal uptake exhibited no stereoselectivity, a pronounced stereoselectivity was found for monoamine oxidase (MAO) [(-)NA〉 (+)NA] as well as for the enzymes which are in series with MAO, namely, aldehyde reductase and aldehyde dehydrogenase [(-)DOPEG〉 (+)DOPEG; (-)DOMA 〈(+)DOMA]. 3. After about 2 h of washout, the efflux of radioactivity from the tissue [which was previously incubated for 30 min with 1.2 μM of either 3H-(-)- or 3H-(±)NA] originated from one neuronal compartment with no stereoselectivity of the rate constant for the efflux of total tritium. The rate-limiting step for the neuronal efflux of tritium resided either in the net efflux of amine from the storage vesicles (normal tissues) or in the net efflux across the axonal membrane (tissues with the amine metabolizing enzymes inhibited). The effects of cocaine and phenoxybenzamine on the neuronal efflux of tritiated compounds strongly depended on the intraneuronal distribution of the 3H-amine. The results indicate that cocaine has only one site of action (neuronal uptake), while phenoxybenzamine exerts reserpine-like as well as cocaine-like effects. 4. The neuronal efflux of tritium from normal tissues preloaded with 3H-(-)- or 3H-(±)NA consisted mainly of amine metabolites (90% of the total; most of this was DOPEG). Since after 2 h of washout the tissue contained hardly any metabolites, these metabolites did not represent pre-formed metabolites (formed during the period of preloading) but newly formed metabolites resulting from the catabolism of the neuronally stored amine. This catabolism was brought about through the activity of presynaptic enzymes and was stereoselective in that more DOPEG, less DOMA and less O-methylated metabolites were formed from (-)-than from (+)NA.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 329 (1985), S. 289-292 
    ISSN: 1432-1912
    Keywords: α2-Agonists ; Salivary secretion ; Postsynaptic α2-adrenoceptors ; Guanabenz ; Guanfacine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of two α2-agonists (guanfacine and guanabenz) on both the submaxillary and parotid gland of the rat were studied. Whereas guanfacine in doses ranging between 1,000 and 30,000 μg/kg i.v. produced an immediate and persistent secretion of saliva from the submaxillary gland, guanabenz in doses as high as 40,000 μg/kg did not induce measurable secretion either from the parotid or the submaxillary gland. Secretion clicited by guanfacine was not modified by yohimbine (300 μg/kg) but was abolished by prazosin (100 μg/kg). In both glands, low doses of either guanabenz (10 μg/kg) or guanfacine (100 μg/kg) markedly inhibited the secretory responses induced by noradrenaline, methacholine and substance P, but not that induced by isoprenaline. The inhibition caused by the α2-agonists was greater for noradrenaline than for either methacholine or substance P. Blockade of α2-adrenoceptors with yohimbine (300 μg/kg) did not modify the response to noradrenaline, methacholine or substance P in either gland. However, the same dose of yohimbine injected 5 min before the α2-agonists prevented the inhibitory effects of guanfacine and guanabenz on the response induced by either one of the three sialagogic agents. Guanabenz (10 μg/kg) did not modify the increase in mean blood pressure observed after the different doses of noradrenaline employed to induce salivary secretion. Guanabenz (10 μg/kg) and guanfacine (100 μg/kg) did not change the time course of the secretion elicited by either noradrenaline, methacholine or substance P, since the degree of inhibition was of similar magnitude at all the periods of time analyzed. The results obtained give further support to the hypothesis that activation of α2-adrenoceptors in the submaxillary as well as parotid gland of the rat inhibits secretory responses which are mediated by either muscarine, substance P and α1-receptors and not those elicited by β-adrenoceptors.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 326 (1984), S. 313-316 
    ISSN: 1432-1912
    Keywords: Salivary secretion ; Postsynaptic α2-adrenoreceptors ; Clonidine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of clonidine on the submaxillary gland of the rat were studied. Doses ranging between 100 to 3.000 μg/kg produced a sustained secretory response which was blocked by 0.1 mg/kg of prazosin but not by 1 mg/kg of yohimbine. Clonidine 10 μg/kg markedly inhibited the salivation induced by noradrenaline, methacholine and substance P but not that induced by isoproterenol. The inhibition caused by the α2-agonist was greater for noradrenaline than for either methacholine or substance P. Blockade of α2 adrenoceptors with yohimbine (0.3–1 mg/kg) prevented the inhibition by clonidine of noradrenaline, methacholine and substance P induced salivation. On the other hand, prazosin 0.1 mg/kg did not modify the inhibition by clonidine of methacholine induced secretion. The results obtained indicate that clonidine exerts a dual effect on salivary secretion: at high doses it elicits salivation through activation of α1-adrenoreceptors; at the dose of 10 μg/kg clonidine activates α2-adrenoreceptors which inhibit the secretory response evoked through either muscarine, substance P and α1-adrenorecptors agonists.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 328 (1984), S. 135-141 
    ISSN: 1432-1912
    Keywords: Adrenergic nerve endings ; Inhibition of MAO ; Saturation of MAO in intact cells ; 3H-(-)-Noradrenaline ; Rat vas deferens
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary After pretreatment of the rats with reserpine and pargyline (to inhibit vesicular uptake and MAO), after an additional in vitro treatment with pargyline, and in the presence of U-0521 (to inhibit COMT), the adrenergic nerve endings of vasa deferentia were loaded with 3H-(-)-noradrenaline by exposure to various concentrations of this amine. Subsequently, tissues were washed out with amine-free solution, and the neuronal efflux of tritium was analysed. 1. During 180 min of wash-out the apparent rate constant for the efflux of tritium decreased with increasing tritium content of the tissue. 2. Prolongation of the wash-out period to 305 min revealed that efflux curves for tritium from heavily loaded tissues became steeper after the 180th min of wash-out. This phenomenon is indicative of saturation (followed by desaturation) of a process that limits the efflux of tritium from heavily loaded tissues. 3. Analysis of the radioactivity of the efflux revealed a characteristic efflux curve for DOPEG: the formation of DOPEG appears to be saturated when the 3H-(-)-noradrenaline content of the tissue is high, in order to become desaturated during prolonged wash-out. These results cannot distinguish between MAO and alcohol dehydrogenase as the saturable enzyme. 4. The formation of the mainly deaminated metabolites (during 60 min of wash-out) was determined in lightly and in heavily loaded tissues. The ratio “formation of metabolites/3H-(-)-noradrenaline content” was lower in heavily than in lightly loaded tissues; the relative decline in DOPEG formation was not accompanied by a compensatory increase in the formation of DOMA. Hence, in heavily loaded tissues, MAO must have been saturated by the pronounced accumulation of axoplasmic 3H-(-)-noradrenaline. 5. From the 100th to the 115th min of wash-out, the fractional rate of loss of DOPEG was negatively correlated with the 3H-(-)-noradrenaline content of the tissue; but no such correlation was observed for the fractional rate of loss of 3H-(-)-noradrenaline. 6. The results are interpreted as indicating that any very pronounced inhibition of intraneuronal MAO (by pargyline) enables the nerve ending to achieve such very high axoplasmic noradrenaline concentrations that two phenomena occur simultaneously: a) there is very little obvious sign of any inhibition of MAO, since the great loss of enzyme activity is largely compensated for by the greatly increased intraneuronal substrate concentration; consequently, DOPEG continues to be formed at a brisk rate; b) the axoplasmic noradrenaline concentration then reaches levels that saturate the intraneuronal enzyme.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 337 (1988), S. 115-117 
    ISSN: 1432-1912
    Keywords: D-1/D-2 receptors ; Reserpine ; Akinesia ; Locomotor activity ; Pergolide ; Sulpiride
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In reserpinized (5 mg/kg, s.c.) mice treated with alpha-methyl-p-tyrosine (200+100 mg/kg, i.p.), increasing doses of the D-2 antagonist sulpiride had varying effects on locomotor activity induced by the mixed D-1/D-2 agonist pergolide (2 mg/kg, s.c.). Low doses of sulpiride (1 mg/kg, i.p.) significantly enhanced this activity whereas at higher doses (50 mg/kg) an inhibitory effect was observed. Amphetamine (3 mg/kg, i.p.) failed to reverse akinesia in this animal model, precluding the possibility of a presynaptically mediated phenomenon; in contrast, mice receiving reserpine alone showed a high degree of locomotor activity when challenged with amphetamine. The bimodal effect of sulpiride is thought to be mediated either by two different D-2 receptors located on the same cell or by the same receptor with different topographical localization on postsynaptic neurons mediating opposite functions.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 389-407 
    ISSN: 1432-1912
    Keywords: Heterotopic heart transplant ; Cardiac denervation ; Noradrenaline ; Isoprenaline ; Supersensitivity of the allografted heart ; Cardiac Rate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A technique for the heterotopic heart transplant into the abdominal cavity of the cat has been developed as an experimental model for studies of the development of sympathetic denervation and of allograft rejection. Under our experimental conditions and in the absence of immunosuppressive treatment the survival rate of the transplant was higher than that reported for dogs. Immediately after the operation the cardiac rate of the transplanted heart was reduced from 153±9 (n=36) to 131±9 beats/min (n=36). After the third postoperative day the rate of the graft increased steadily, reaching 185±8 beats/min (n=15) on the seventh day. The endogenous noradrenaline (NA) content in the right atrium was completely depleted 3 days after the operation (controls 2.07±0.45 μg NA/g; transplants 0.09±0.04 μg NA/g). In the ventricles a similar degree of depletion was obtained on the seventh postoperative day (controls 1.69±0.25 μg NA/g; transplants 0.06±0.02 μg NA/g). “In vitro” studies of strips of left atria revealed supersensitivity to the inotropic effect of (−)-noradrenaline 7 days after the surgical procedures. On the 7th day maximal responses of the atria to (−)-noradrenaline were significantly lower than those of the corresponding controls. There was no increase in sensitivity to (−)-isoprenaline 7 days after the operation. The results obtained demonstrate that the transplanted heart undergoes sympathetic denervation and develops supersensitivity to noradrenaline. The latter appears to be the reason for the tachycardia which develops between the third and the seventh day after the operation.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 298 (1977), S. 245-253 
    ISSN: 1432-1912
    Keywords: 6-Hydroxydopamine ; Supersensitivity ; Chemical denervation ; Degeneration secretion ; Sympathectomy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Injection of 6-hydroxydopamine (6-OH-DA) elicited a marked and sustained secretory response of control and surgically sympathectomized submaxillary glands of rats. These responses were diminished by previous treatment with reserpine 0.1 mg/kg 48 and 24h before the experiment and almost abolished by 5 mg/kg reserpine 6 h before the administration of 6-OH-DA. The responses to 6-OH-DA were potentiated in control glands by previous preganglionic denervation of either the parasympathetic or sympathetic nerves of the gland. Development of postjunctional supersensitivity in denervated glands also increased the responses to 6-OH-DA, while atropine had a feeble blocking action. For all these responses, the adrenal catecholamines played no role. After two consecutive doses of 6-OH-DA a third dose of the drug still elicited a secretory response that was 50% of that of the first dose. It is concluded that for the responses to 6-OH-DA the leakage of noradrenaline from the degenerating adrenergic nerve endings of the submaxillary gland plays a partial role. Noradrenaline released by the drug from other tissues and reaching the gland via the circulation also contributes to the responses observed. A muscarinic component may also participate in the secretory effects of 6-OH-DA.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-1912
    Keywords: Submaxillary glands ; Presynaptic receptors ; Potassium ; Phentolamine ; Transmitter release ; Noradrenaline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Fifteen days after duct ligation, the wet weight of the rat submaxillary gland was reduced to 40% of the contralateral control. Under these experimental conditions, the noradrenaline (NA) content expressed as μg/g was 1.2±0.1 in the control glands and 1.9±0.2 in the atrophied glands. The accumulation of 3H-NA in the tissue expressed as μCi/gland, did not differ when the atrophied glands were compared with the corresponding controls. Consequently, the uptake and retention of 3H-NA was not modified by the atrophy of the secretory cells of the gland. The spontaneous efflux of radioactivity from normal and atrophied submaxillary glands prelabelled with 3H-NA was similar. The analysis of the metabolic pattern in both experimental groups revealed that in the spontaneous outflow and also during potassium-induced depolarization, the formation of the O-methylated metabolite, 3H-normetanephrine (NMN) was reduced by more than 50% in the atrophied glands. During depolarization induced by K+, a 2-fold increase in the outflow of the deaminated glycol 3H-3,4-dihydroxyphenylglycol (DOPEG) was observed. The effect of phentolamine on the release of radioactivity induced by 60 mM K+ in normal and in atrophied submaxillary gland slices prelabelled with 3H-NA was also investigated. In both experimental groups, the fractional release of total radioactivity induced by K+ was similar. Phentolamine, 3.1 μM, produced a 3-fold increase in the fractional release of radioactivity both in the control and the atrophied glands. These results indicate that the increase of K+-induced release of 3H-NA induced by phentolamine was independent of the presence or absence of the postsynaptic structures. It is concluded that phentolamine increases transmitter release by blocking alpha-adrenoceptors located in the noradrenergic nerve endings of the rat submaxillary gland.
    Type of Medium: Electronic Resource
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