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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 86 (1985), S. 270-273 
    ISSN: 1432-2072
    Keywords: Hashish extract ; Δ 9-Tetrahydrocannabinol ; Social learning model ; Submissive behavior ; Retention deficit ; State dependency ; Analgesia ; C3H mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of hashish extract on adaptive behavior of male mice were studied in a paradigm which allows the investigation of learning mechanisms in a social context. Mice of the C3H strain, which were not submissive in a confrontation with a nonaggressive DBA mouse on day 1, were defeated on day 2 over 3 min by aggressive, isolated DBA mice, and showed conditioned submissive behavior upon mere contact with a nonaggressive DBA mouse on day 3. A hashish extract containing 38.6–39.4% Δ 9-tetrahydrocannabinol (Δ 9-THC), 11.6–12.0% cannabinol and 47.7–48.5% cannabidiol was administered orally in all experiments. Hashish extract given 90 min before defeat on day 2, in dosages corresponding to 1, 5, and 10 mg Δ 9-THC/kg, impaired retention of defensive upright, defensive sideways and immobility on day 3 (experiment 1). Experiment 2 showed that the drug (5, and 10 mg Δ 9-THC/kg) had no antinociceptive potency in mice and did not modify defeat-induced analgesia. Experiment 3, with drug (5 mg Δ 9-THC/kg) or solvent administration on day 2 and day 3, showed that the retention deficit was neither due to state-dependent learning, nor to impaired retrieval. It is suggested that hashish extract administered before learning may interfere with memory processing.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 40 (1957), S. 888-906 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird die Synthese von substituierten β-Amino-tetrahydrofuranen und deren quaternären Salzen beschrieben. Als Ausgangsmaterialien dienten entweder γ-Lactone oder α-Acetylenketone oder Furan-3-carbonsäure. Von den [2-(α-Hydroxyäthy1)-tetrahydro-furyl-(4)]-trimethylammonium-Verbindungen wurden zwei Racemate isoliert, die sich als verschieden von Muscarin erwiesen. Katalytische Oxydation rnit Platin-Sauerstoff ergab beim Muscarin ein Keton (Ketomuscarin), dessen IR.-Spektrum auf ein Fünfring-Keton schliessen lässt. Aus dem Verhalten des Ketomuscarins gegenüber Alkali ist zu schliessen, dass die Trimethylammoniumgruppe nicht in α- oder β-Stellung zur Carbonylgruppe stehen kann, und dass dem Muscarin folglich Formel III zuzuweisen ist.Die pharmakologische Prüfung der synthetischen Produkte an Froschorganen und Katzen auf muscarinische, nikotinische und curareartige Wirkungen ergab eine gegenüber Muscarin geringere muscarin-, hingegen verstärkte nikotin- und curareartige Wirksamkeit.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Furan-4-carbonester lassen sich mit Dimethylformamid und Phosphoroxychlorid in Stellung 2 formylieren. Die reduktive Aminierung der Aldehydgruppe gelingt katalytisch mittels LINDLAR-Katalysator ohne überwiegenden EMDE-Abbau.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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