Effects of alpha-methyl tyrosine and adrenergic blocking agents on the facilitating action of amphetamine and nicotine on learning in rats
β Scribed by Otto A. Orsingher; Susana Fulginiti
- Publisher
- Springer
- Year
- 1971
- Tongue
- English
- Weight
- 567 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0033-3158
No coin nor oath required. For personal study only.
β¦ Synopsis
DL-amphetamine sulphate (2mg/kg) and nicotine (0.2mg/kg) showed a facilitatory action on the acquisition of a conditioned response in a shuttle-box by rats and this was reversed by pretreatment with ~-MT (30 mg/kg).
Pretreatment with dibenamine (10mg/kg) impaired the action either of amphetamine or nicotine. Nethalide (5--10 mg/kg) exerted a partial protection on the depressant effect produced by the interaction between dibenamine and nicotine.
Animals treated with a-MT (30 mg/kg) and kept in the cold (4--6 ~ C for 3 h) also showed a depressed learning capacity.
DL-Dopa (200 mg/kg) provided a partial protection on the depressive effects caused by the interaction of a-MT with amphetamine, nicotine or cold. It is suggested that the facilitutory learning action of amphetamine and nicotine involves a common adrenergic mechanism. The depressant effects of amphetamine, nicotine or cold after a-MT treatment are attributed to depletion of "functional pools" of catecholamines.
π SIMILAR VOLUMES
Rats were trained to perform in discrimination learning reinforced by water for 6 days, and were intraperitoneally injected with chlorpromazine, reserpine, or d-amphetamine after each training session. Although chlorpromazineat the dose levels of 0.5 rag/ kg or more injected immediately after traini
A test of attentional switching was devised for the rat in which it obtained sucrose reinforcement by an appropriate nose-poke response that discriminated which of two visual events terminated first, in a specially designed chamber. The effect of mesolimbic dopamine depletion (to 20% of control valu
The purpose of this investigation was to determine if the reported prolongation of barbiturate-and ethanol-induced sleeping times by nicotine in rodents are pharmacodynamic or pharmacokinetic interactions. Adult female rats were pretreated with nicotine, either 0.5 or 1.5 mg/kg ip acutely or 0.5 mg/