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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 35 (1974), S. 237-241 
    ISSN: 1432-2072
    Keywords: Morphine ; Phenobarbital ; Ethanol ; Amphetamine ; Aggression ; Rearing ; Biting ; Vocalization ; Paw Shock ; Drug Dependence ; Withdrawal Syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Male rats of Long-Evans strain were chronically administered increasing doses until a maximally tolerated maintenance-dose of morphine (400 mg/ kg/day), phenobarbital (400 mg/kg/day), ethanol (20ml of 50% v/v/day) or amphetamine (16 mg/kg/day) was reached. After several days of maintenance doses, the rats were withdrawn from those drugs. When grouped, morphine-withdrawn rats showed intermittent spontaneous-aggression (rearing, vocalization, attack-bites). Amphetamine (2 mg/kg) treatment potentiated morphine withdrawal aggression. However, animals withdrawn from phenobarbital, ethanol or amphetamine failed to show spontaneous aggression with or without amphetamine. Similarly, shock intensity required to elicit pain-induced aggression was significantly decreased in morphine-withdrawn rats but not in rats withdrawn from phenobarbital, ethanol or amphetamine. These results suggest that the aggression seen during abstinence is caused by specific changes in the central nervous system uniquely produced by the chronic administration of narcotic drugs.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 32 (1973), S. 113-120 
    ISSN: 1432-2072
    Keywords: l-Dihydroxyphenylalanine ; dl-Dihydroxyphenylalanine ; d-Amphetamine ; Alpha Methyl-p-Tyrosine ; Haloperidol ; Methadone ; Morphine ; Aggression ; Rearing ; Vocalization ; Biting ; Dopaminergic Neuropathway ; Supersensitivity ; Narcotic Addiction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Aggregation during morphine abstinence elicited social aggression (rearing, vocalization, attack-bites) in the morphine dependent rats. Pretreatment with l-dihydroxyphenylalanine (50 mg/kg), dl-dihydroxyphenylalanine (200 mg/ kg), dextro-amphetamine sulfate (2 mg/kg) or apomorphine hydrochloride (1.25 mg/kg) enhanced that aggression severalfold. Alpha methyl-p-tyrosine (200 mg/kg) abolished the morphine withdrawal aggression that was elicited either by mere aggregation or by aggregation combined with amphetamine. However, alpha methyl-p-tyrosine did not block the aggression in apomorphine treated rats. Haloperidol (0.63–2.5 mg/kg) also blocked the aggression due to mere abstinence or abstinence supersensitized by amphetamine. Similarly, methadone hydrochloride (5–20 mg/kg) blocked morphine withdrawal aggression supersensitized by apomorphine. These data are interpreted to suggest dopaminergic basis of morphine withdrawal aggression and a latent supersensitivity of dopaminergic neuropathways during morphine dependence.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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