ArticleBehavioural pharmacology2011
Importance of associative learning processes for one-trial behavioral sensitization of preweanling rats.
Article in Behavioural pharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Importance of D1 and D2 receptor stimulation for the induction and expression of cocaine-induced behavioral sensitization in preweanling rats.Behavioural brain research · 2017Article
- Context- and time-dependent neurobiological and behavioral sensitization induced by a single morphine exposure in mice.Psychopharmacology · 2016Article
- Effects of D2 or combined D1/D2 receptor antagonism on the methamphetamine-induced one-trial and multi-trial behavioral sensitization of preweanling rats.Psychopharmacology · 2016Article
- Effects of nicotine on ethanol-induced locomotor sensitization: A model of neuroadaptation.Behavioural brain research · 2015Article
- Age-dependent differences in the strength and persistence of psychostimulant-induced conditioned activity in rats: effects of a single environment-cocaine pairing.Behavioural pharmacology · 2014Article
- Role of the D1 receptor for the dopamine agonist-induced one-trial behavioral sensitization of preweanling rats.Psychopharmacology · 2014Article
- Early ontogeny of D-amphetamine-induced one-trial behavioral sensitization.Pharmacology, biochemistry, and behavior · 2013Article
- Ontogeny of methamphetamine-induced and cocaine-induced one-trial behavioral sensitization in preweanling and adolescent rats.Behavioural pharmacology · 2012Article
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7 authors.
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Abstract
During adulthood, associative learning is necessary for the expression of one-trial behavioral sensitization; however, it is uncertain whether the same associative processes are operative during the preweanling period. Two strategies were used to assess the importance of associative learning for one-trial behavioral sensitization of preweanling rats. In the initial experiments, we varied both the sequence and time interval between presentation of the conditioned stimulus (CS, novel environment) and unconditioned stimulus (US, cocaine). In the final experiment, we determined whether electroconvulsive shock-induced retrograde amnesia would disrupt one-trial behavioral sensitization. Results showed that robust-sensitized responding was apparent regardless of the sequence in which cocaine and the novel environment (the presumptive CS) were presented. Varying the time between CS and US presentation (0, 3, or 6 h) was also without effect. Results from experiment 3 showed that single or multiple electroconvulsive shock treatments did not alter the expression of the sensitized response. Therefore, these data indicated that one-trial behavioral sensitization of preweanling rats was exclusively mediated by nonassociative mechanisms and that associative processes did not modulate sensitized responding. These findings are in contrast to what is observed during adulthood, as adult rats exhibit one-trial behavioral sensitization only when associative processes are operative.
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