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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 20 (1973), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The Presence of endogenous 2-phenylethylamine in mammalian tissues has long been suspected, in view of the fact that L-phenylanine, a substrate for L-aromatic amino acid decarboxylase (Lovenberg, Weissbach and Udenfriend, 1962), is found in substantial amounts in many neural and non-neural tissues. It has been difficult to demonstrate the presence of phenylethylamine in tissues of untreated animals because this amine is an excellent substrate for monoamine oxidase (Mantegazza and Riva, 1963). Using paper chromatography and electrophoresis, Nakajima, Kakimoto and Sano (1964) tentatively identified phenylethylamine in many organs of animals pretreated with monoamine oxidase inhibitors. Phenylethylamine exerts, in animals pretreated with such inhibitors, behavioural stimulant effects similar to those induced by amphetamine (Mantegazza and Riva, 1963). These effects may in part be attributable to catecholamine release (Fuxe, Grobecker and Jonsson, 1967) and partly to a direct effect exerted by phenylethylamine itself (Fischer, Ludmer and Sabelli, 1967; Giardina, Pedemonte and Sabelli, 1972). The brain content of phenylethylamine in mice (Mosnaim and Sabelli, 1971), rabbits (Sabelli, Giardina, Mosnaim and Inwang, 1972) and rats (Fischer, Spatz, Heller and Reggiani, 1972) is increased by antidepressive treatments (imipramine, monoamine oxidase inhibitors, electroshock) and reduced by reserpine. The urinary excretion of phenylethylamine is decreased in depressed patients (Fischer, Heller and Miró, 1968; Boulton and Milward, 1971; Inwang, Sugerman, Mosnaim and Sabelli, 1972; Fischeret al., 1972).However, the presence of phenylethylamine in brain has not yet been conclusively demonstrated because the analytical procedures used in the above-mentioned investigations were not sufficiently specific. In the present study we isolated and identified, by a number of analytical procedures, phenylethylamine and its metabolite 2-hydroxy-2-phenylethylamine (phenylethanolamine) from human brain. Molinoff, Landsberg and Axelrod (1969) have shown by enzymatic methods the formation of phenylethanolamine following the administration of phenylethylamine.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 187 (1960), S. 784-785 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The results obtained with norepinephrine, epine-phrine, phenylephrine, ephedrine, d-I-amphetamine, d-amphetamine, and mephentermine confirmed that reserpine potentiates or leaves unchanged the motor effects of catechol or phenolethanolamines, but inhibits those of phenylethanolamines reversibly and ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 248 (1974), S. 144-145 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Brain levels of 2-phenylethylamine were determined in rabbits (New Zealand, male, 2-3 kg) using the method of Mosnaim and Inwang15, which measures the ultraviolet absorbance at 287 nm of the reaction product of PEA with eerie sulphate and HC1. For behavioural observation, ten male white Swiss mice ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 223 (1969), S. 73-74 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Electrophysiological studies were conducted in un-anaesthetized rabbits with chronically implanted epidural electrodes. The evoked response was elicited by a 10 ms red flash presented once every 2 s during a 2-3 h session. Optic cortex potentials were recorded monopolarly. Fifty evoked responses ...
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 27 (1971), S. 64-65 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Resumen El estudio de la curva dosis-respuesta demuestra que el 5-hidroxi-triptofol y el acido 5-hidroxi-indolacético son tan potentes como la serotonina en modificar las respuestas corticales ópticas en el conejo. Pretratamiento con pargilina o con disulfiram, dos inhibidores distintos del metabolismo de las neuroaminas, influenció marcadamente los efectos de la serotonina sin cambiar los efectos de sus metabolitos.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 26 (1970), S. 48-49 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Resumen La adrenalina (0.1 a 0.5 mg/rana) hiperpolarizó los hepatocitos deR. pipiens y depolarizó a dosis mas altas. El inhibidor de la monoamino oxidasa pargilina (100 mg/kg, 24–48 h antes) impidió este efecto.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 26 (1970), S. 58-60 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Resumen En el conejo no anestesiado, el acido 5-hidroxiindoleacético y el 5-hidroxitriptofol modifican los potenciales ópticos evocados de manera similar que la serotonina. Los derivados deaminados de la serotonina probablemente modulan las sinápsis serotonérgicas.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 31 (1975), S. 1049-1051 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The microiontophoretic administration of putative neuromodulators (acetylcholine, norepinephrine, dopamine, 2-phenylethylamine, tryptamine, histamine) triggered firing or inhibited on-going activity in isolated frog sciatic nerves.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 42 (1975), S. 117-125 
    ISSN: 1432-2072
    Keywords: Phenylethylamine ; Phenylethanolamine ; Neuromodulators ; Evoked Responses ; Electroshock ; Mouse Behavior ; Rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The electrophysiological and behavioral effects of phenylethanolamine (OHPEA) and of its precursor 2-phenylethylamine (PEA) were studied in mice and rabbits. In animals pretreated with MAOI, PEA was found to exert strong amphetamine-like effects, EEG alerting, reduction of visual evoked responses, increased locomotor activity, and blockade of tonic seizures induced by electroshock. OHPEA exerted weaker amphetamine-like effects. Inhibition of dopamine-Β-hydroxylase increased most of the effects of PEA. In non-pretreated animals, OHPEA was found to shorten electroshock latency and to prolong the duration of visual evoked responses. PEA (but not OHPEA) potentiated the excitement induced by δ9-tetrahydrocannabinol in MAOI-pretreated mice. Reserpine pretreatment reduced but did not abolish the CNS effects of OHPEA and PEA. One may speculate that endogenous PEA is more likely to serve as a modulator for ergotropic functions than is endogenous OHPEA.
    Type of Medium: Electronic Resource
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