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  • 1
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    Unknown
    Washington, etc. : Periodicals Archive Online (PAO)
    Explicator. 25:6 (1967:Feb.) 
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  • 2
    ISSN: 1432-2072
    Keywords: Fetus ; Prenatal drug exposure ; Schizophreniad-Amphetamine ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Recent evidence suggests that mid-pregnancy is a critical period for production of fetal abnormalities that cause behavioral and neuropathological changes in adult offspring. The present experiments provide an animal model of these effects by treating pregnant Sprague-Dawley rats during gestational days 11–14 withd-amphetamine (AM). Offspring were tested for neurological signs, foraging activity, reversal learning, and sensitivity to amphetamine challenge. In the Early Juvenile period, postnatal days (PND) 20–30, female AM offspring initially showed reductions in rearing, holepoking, and midfield activity. On later trials, and as young adults, AM females showed signs of locomotor hyperactivity despite continued poor foraging efficiency, and were also more sensitive to a 1.0 mg/kgd-amphetamine challenge. AM males showed initially slower and more perseverative responding than controls, but then developed excessive response switching. These changes continued during tests for Retention, Reversal, and Extinction in the Late Juvenile/Early Adult stage (PND 50–90), when both AM-exposed sexes showed increased eating time, significantly more perseverative lateral turning preference (right or left), and slower reversal learning than controls. Behavioral data were consistent with aberrations in thalamo-frontal and mesolimbic/nigrostriatal projection systems that have been reported in AM animals and which are also affected by maternal drug abuse and schizophrenia.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: Amphetamine ; Apomorphine ; Neuroleptics ; Dopamine ; Drinking Behaviour ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Hypodipsia produced by injection of d-amphetamine (2.0 mg/kg) or apomorphine (0.8 mg/kg) in rats, was partially antagonized by two DA-specific neuroleptic drugs, Pimozide and Spiramide, respectively. Pimozide revealed a maximal amphetamine-antagonistic effect at dose levels between 0.1–0.4 mg/kg. Hypodipsia could also be produced by Pimozide alone in doses greater than 1.0 mg/kg. Pretreatment of the apomorphine-induced hypodipsia with 0.05 mg/kg Spiramide also reliably counteracted drinking deficits. The interaction of water deprivation combined with the presence or absence of food in the test situation was also examined, but no effect was found. The possibility that perseverative rearing on the hind legs under d-amphetamine might interfere with drinking was tested with high vs. low drinking-tubes in the Pimozide-amphetamine experiments. There was evidence for a slight initial effect of drinking position, but the general form of the dose-response curve was not greatly altered. It was concluded that dopamine effects cannot easily be excluded from a role in the control of drinking, and that the primary role often accorded norepinephrine in relation to amphetamine effects should be re-examined with respect to the specific behavioural functions which are altered.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: flupenthixol ; Long-term treatment ; Cell loss ; Corpus striatum ; Neuroleptics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The number of nerve cells in two different areas of the corpus striatum (i.e., ventrolateral and dorsomedial) was estimated in rat brain after long-term (36 weeks) treatment with the neuroleptic flupenthixol. Nine rats were given weekly injections of 4 mg/kg flupenthixol dissolved in Viscoleo® i.m., and seven rats received Viscoleo® alone. Fourteen to 18 weeks after the last drug injection, the animals were decapitated and half of each brain was fixated with formalin for cellcount analysis and the remaining half used for a biochemical analysis (Nielsen, 1977). Separate cell counts in the ventrolateral and dorsomedial corpus striatum yielded a significant cell loss of approximately 10%, but only in the ventrolateral striatum of treated animals. These results suggest at least one concrete anatomical basis for the behavioral and biochemical deficits found in the same animals, as reported earlier. The results further suggest that persistent irreversible anatomical changes can follow long-term neuroleptic treatment. The inconsistencies of results regarding cell loss in the corpus striatum may be due to neglect of dorsal-ventral structural differences in corpus striatum.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2072
    Keywords: Operant Conditioning ; Amphetamine ; Animal Behaviour ; Stereotypy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two experiments were performed in rats, using operant conditioning techniques and various dose levels of d-amphetamine. Repeated sessions with drugs occurred at intervals of at least four days and were interspersed with saline or non-injection control sessions so that results from each animal could be compared with its own control data. Each animal was tested on one of two schedules of reinforcement, both of which used termination of electric shock as the principle response-contingent event. In the first schedule (Av-R), each lever-press in the presence of shock was followed by a period of no-shock and each subsequent lever-press within this no-shock period further delayed the onset of shock. In the second schedule (Av-H), the shock was off only as long as the animal held the lever in a depressed position and leverrelease was immediately followed by shock. At 1.0 mg/kg d-amphetamine, total avoidance of shock, as compared with control sessions, was increased on the Av-R schedule, but deteriorated on the Av-H schedule, in both cases due to increased lever-pressing (and releasing). At higher doses of 3.0–5.0 mg/kg, shock avoidance responding on the Av-R schedule was even higher in some animals but decreased or disappeared in others, while holding activity on the Av-H schedule was practically unaffected except in very long sessions. Recording of other bodily activities during these sessions revealed dose-related elements of response perseveration and behavioural stereotypy which could be more effectively blended with Av-R responding at low doses and with Av-H responding at higher doses. These results were discussed in relation to the operant conditioning literature on behavioural effects of amphetamine and a theoretical link was suggested between increasingly stereotyped behaviour due to the drug effect and the type of responding seen in the two schedules tested here.
    Type of Medium: Electronic Resource
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