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  • 1
    ISSN: 1432-2072
    Keywords: Key wordsd-Amphetamine ; Haloperidol ; Procedural learning ; Automatic processing ; Dopamine ; Neuroleptic medication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of an indirect dopamine-agonist, d-amphetamine, and a non-selective dopamine receptor antagonist, haloperidol, were investigated in normal male volunteers using a between-subjects double-blind design in a procedural learning task, thought mainly to involve unconscious/automatic learning. The results showed: (1) d-amphetamine facilitated response speed, whereas haloperidol inhibited it, in comparison to placebo; (2) the linear increase in procedural learning corresponded with pharmacological manipulation of degree of dopaminergic activity, i.e. subjects given haloperidol showed the least, and subjects given d-amphetamine the greatest, procedural learning. The implications of these findings are discussed in relation to investigation of abnormalities of procedural learning processes in schizophrenia.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: 5-Hydroxytryptophan ; Serotonin ; Neuroleptics ; Methysergide ; Dopamine ; Hyper-sensitivity ; Apomorphine ; Amphetamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract It has been proposed that prolonged pharmacologic blockade of specific receptor sites by specific antagonists results in specific denervation hypersensitivity. The exact specificity of such antagonist-induced behavioral hypersensitivity has not previously been investigated. The present study was undertaken to determine whether hypersensitivity induced by a chronic dopamine antagonist (chlorpromazine or haloperidol) and by a serotonin antagonist (methysergide) is specific to their respective agonists or whether the induced physiologic alterations are more generalized. Chlorpromazine, haloperidol, or methysergide was given to guinea pigs daily for 21 days and the subsequent behavioral responses to d-amphetamine, apomorphine, and d,l-5-hydroxytryptophan were observed. Chronic dopaminergic antagonism resulted in hypersensitivity to dopamine agonism but did not change the response to serotonin agonism as gauged by 5-hydroxytryptophan-induced stereotypy. Chronic serotonin antagonism was shown to result in hypersensitivity to serotonin agonism, which was not associated with any increase in the behavioral response to either direct or indirect dopamine antagonists. These findings indicate that the chronic administration of dopamine and serotonin antagonists results in behavioral hypersensitivity, which is limited to the system antagonized, and that antagonist-induced hypersensitivity involves the transmitter-specific receptors blocked by the antagonist in question.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: Dopamine ; Noradrenaline ; Caudate nucleus ; Cats ; Annual rhythm ; Behaviour
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two aspects of the functional interaction between the neurotransmitters dopamine (DA) and noradrenaline (NE) were studied: the role of NE within brain structures marked by DA terminals and the occurrence of annual changes in their functional interaction. The behavioral changes produced by single or combined administration of DA, (3,4-dihydroxyphenylamino)-2-imidazoline (DPI), ergometrine, ET-495, NE, oxymetazoline, and phentolamine into the caudate nucleus of freely moving cats were analyzed. NE and oxymetazoline produced effects that differed from those elicited by DA or DPI. NE-dependent effects were antagonized by phentolamine, and DA- or DPI-induced effects were antagonized by ergometrine. Ergometrine, NE, and oxymetazoline were effective in November, December, and January, lost their effectiveness in March, April, and May, regained it in July, and lost it again in August, September, and October. The annual pattern of DA, DPI, and phentolamine on the other hand, was just the opposite. DA agonists suppressed NE- or oxymetazoline-induced effects, while the DA antagonist suppressed phentolamine-induced effects. Noradrenergic agents were unable to modulate the DA-dependent effects under certain circumstances. It is concluded that (1) NE-dependent processes within the feline caudate nucleus inhibit DA-dependent processes within this structure, and (2) there exists a reciprocal relationship between the annual changes in the feline's susceptibility to DA, DPI, and phentolamine, on the one hand, and to ergometrine, NE, and oxymetazoline, on the other hand.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: Chronic schizophrenic ; Type ; Serotonin ; Dopamine ; Setoperone ; Autism ; Mood ; Parkinson ; Extrapyramidal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The new antipsychotic drug setoperone is pharmacologically characterized by its potent serotonin and moderate dopamine receptor blocking properties. Forty chronic schizophrenic patients were included and 34 completed this pilot study. Following a drug free period of 1 week the patients received setoperone 5 mg t.i.d. After 1 month of treatment, the psychotic symptoms, as measured by the BPRS, improved by approximately 50% (P〈0.001) as compared with the condition under previous neuroleptic medication. Blockade of serotonin receptors may be related to improvement of autistic behaviour, dysphoria, and parkinson-like symptoms. In residual schizophrenic patients, the need for dopamine blockade, which is normally correlated with the therapeutic effect on positive symptoms, can be reduced substantially.
    Type of Medium: Electronic Resource
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