2006
DOI: 10.1007/s00213-005-0259-1
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Contribution of drug doses and conditioning periods to psychomotor stimulant sensitization

Abstract: Repeated association of the peak behavioral effects of high doses of amphetamine or cocaine with the drug-paired environment produces maximal expression of sensitized locomotor responses. Certain testing conditions appear to disrupt sensitization to these same doses of the drugs.

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Cited by 24 publications
(16 citation statements)
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“…Following 10 mg/kg IP cocaine injections, locomotor sensitization emerged rapidly in cocaine-preferring but not saline-preferring postpartum females after only four exposures, replicating the induction phase of sensitization reported by others (Post and Rose 1976) and supporting proposed correlations between cocaine's motoric and motivational effects (Wise and Bozarth 1987). This locomotor sensitization emerged using short (30 min) conditioning sessions, indicating that longer (60-120 min) exposures are not necessary to produce sensitization to 10 mg/kg IP cocaine (Todtenkopf and Carlezon 2006). Locomotor sensitization did not emerge in cocaine-preferring females given 20 mg/kg IP, possibly due to the number of subjects (i.e., power) or relatively large variability.…”
Section: Locomotion Across the Cpp Proceduressupporting
confidence: 81%
See 1 more Smart Citation
“…Following 10 mg/kg IP cocaine injections, locomotor sensitization emerged rapidly in cocaine-preferring but not saline-preferring postpartum females after only four exposures, replicating the induction phase of sensitization reported by others (Post and Rose 1976) and supporting proposed correlations between cocaine's motoric and motivational effects (Wise and Bozarth 1987). This locomotor sensitization emerged using short (30 min) conditioning sessions, indicating that longer (60-120 min) exposures are not necessary to produce sensitization to 10 mg/kg IP cocaine (Todtenkopf and Carlezon 2006). Locomotor sensitization did not emerge in cocaine-preferring females given 20 mg/kg IP, possibly due to the number of subjects (i.e., power) or relatively large variability.…”
Section: Locomotion Across the Cpp Proceduressupporting
confidence: 81%
“…Our characterization of cocaine-induced locomotion and the induction phase of motoric sensitization in the postpartum female during conditioning sessions with IP cocaine builds upon existing dose-response locomotor analyses in males and cycling female rats (Sell et al 2000;Hu and Becker 2003;Todtenkopf and Carlezon 2006). Locomotion during CPP testing characterizes subjects' behavioral responsivity to cocaine-and saline-associated chambers during their expression of conditioned chamber preference, offering unique insight into individual differences in motivation (Seip and Morrell 2007) and extending prior CPP work using other abused drugs (Parker 1992).…”
Section: Introductionmentioning
confidence: 98%
“…However, these brain regions are critical integrators of sensori-motor, affective, and cognitive information, and therefore the behavioral effects of cocaine are determined not only by its pharmacological properties, but also the physiological and contextual states of the animal (Barrett, 1987;Falk and Feingold, 1987). For example, prior drug experience, stress and the environment in which cocaine is administered have been shown to modulate behavioral responses to acute and chronic cocaine (Robinson and Berridge, 1993;Shaham et al, 2003;Badiani and Robinson, 2004;Todtenkopf and Carlezon, 2006). These factors are thought to contribute to the development and maintenance of addiction (Koob and Le Moal, 1997;Lu et al, 2003).…”
Section: Introductionmentioning
confidence: 99%
“…Previous investigations of cocaine effects on locomotor activity with rodents have typically utilized a trial length of 60 min or less [20,21,22]. Figure 3 represents the mean photobeam breaks for the first 60 min of the 150 min trial for groups that received saline, or 5, 10, or 20 mg/kg cocaine.…”
Section: Resultsmentioning
confidence: 99%