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  • Chemistry  (2)
  • Cycloheximide  (2)
  • Chlorpromazine  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Psychopharmacology 21 (1971), S. 309-316 
    ISSN: 1432-2072
    Schlagwort(e): Memory ; Mice ; PassiveAvoidance ; Cycloheximide ; Detention
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract After training in a passive avoidance task, mice were detained in the safe compartment of the conditioning apparatus. This detention produced an impairment of rentention on the retest trial. Detention did not prolong the cycloheximide susceptible phase of memory formation. A summation of the amnestic effects of the two treatments occurred only at a time when both were effective alone. Cycloheximide was without effect upon the detention experience itself.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Psychopharmacology 16 (1969), S. 147-155 
    ISSN: 1432-2072
    Schlagwort(e): Amphetamine ; Chlorpromazine ; Scopolamine ; Drug Interactions ; Delayed Matching
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Two drug combinations, amphetamine-chlorpromazine and amphetamine-scopolamine, were examined in monkeys performing on a delayed matching test. Antagonism between the effects of amphetamine and chlorpromazine on both response rate and accuracy measures of performance was found. Amphetamine and scopolamine had antagonistic effects on response rate but synergistic effects on accuracy.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1432-2072
    Schlagwort(e): Memory ; Mice ; Cycloheximide ; Electroconvulsive Shock ; Passive Avoidance ; Strength of Conditioning
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Delay of punishment 0, 30, 60, 120 and 240 sec after the step-through response in a one trial passive avoidance task was used to obtain in mice conditioned responses of different strengths. Both cycloheximide and ECS given immediately after training had a greater amnesic effect upon the weaker conditioned responses obtained with the longer delays of punishment. A proactive effect of ECS, but not of cycloheximide, was demonstrated with the weaker conditioned responses.
    Materialart: Digitale Medien
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  • 4
    ISSN: 0899-0042
    Schlagwort(e): chiral pharmacokinetics ; rac-flurbiprofen ; rat ; bone pharmacodynamics ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The route of administration of the NSAID, flurbiprofen (sq vs. po) resulted in positive and negative results respectively with regard to enhanced cancellous and cortical bone accumulation in the immature rat. This pharmacokinetic study was an effort to understand the pharmacodynamic difference between the two routes of administration observed when the same dose range of drug, given as single daily doses, had been employed in both studies. Conventional chiral pharmacokinetics were evaluated in young rats. A significant difference was observed in the Tmax of the active (S)-enantiomer by both administration routes (sq 4 h and po 1 h). The bioavailability, as evaluated by AUCs favored the sq route as expected. The plasma concentrations over 18 h, at steady state, for one po dose group (0.5 mg/kg/day) fell well within the therapeutic window described by the 0.1 and 0.5 mg/kg sq doses which had demonstrated anabolic bone activity. Oral dosing had exhibited no significant bone activity. We conclude that the pharmacodynamic difference between routes of administration cannot be simply explained on a pahrmacokinetic basis. Consequently, experiments detailing the pharmacodynamics and pharmacokinetics of single and multiple dose administration of aryl-propionic acids in normal and osteopenic states need further pharmacologic study. © 1994 Wiley-Liss, Inc.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 5 (1993), S. 492-494 
    ISSN: 0899-0042
    Schlagwort(e): GI-side effects ; NSAID ; ulcerogenicity ; rac-flurbiprofen enantiomers ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The most common, and sometimes life-threatening, side-effects associated with the human use of the analgesic, nonsteroidal antiinflammatory drugs (NSAIDs) are gastrointestinal. These include gastritis, ulceration, and severe bleeding. The aryl propionic acid class of NSAIDs are among the most widely used of these drugs in the world, including rac-ibuprofen, rac-flurbiprofen, and rac-ketoprofen. Marketed as racemates, it was assumed that the “inactive” (R)-enantiomers, having no cyclooxygenase inhibiting effect, also had no toxic effect. In a 30-day dose response study of (S)-, (R)-, and rac-flurbiprofen given daily over a range of doses the (R)-isomer alone proved to be without apparent gastrointestinal (GI) toxicity. On the other hand the racemate proved to be 2 to 4 times as ulcerogenic in enantiomerically equivalent doses as the (S)-enantiomer. These results have significant clinical implications. © 1993 Wiley-Liss, Inc.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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