COCAINE-INDUCED CONDITIONED LOCOMOTION - ABSENCE OF ASSOCIATED INCREASES IN DOPAMINE RELEASE
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作者:
BROWN, EE
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UNIV BRITISH COLUMBIA, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADAUNIV BRITISH COLUMBIA, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADA
BROWN, EE
[1
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FIBIGER, HC
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UNIV BRITISH COLUMBIA, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADAUNIV BRITISH COLUMBIA, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADA
FIBIGER, HC
[1
]
机构:
[1] UNIV BRITISH COLUMBIA, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADA
The potent reinforcing effects of cocaine can readily become associated with salient environmental stimuli that acquire secondary reinforcing properties. This phenomenon is of considerable significance as intense craving can be evoked by stimuli previously associated with the effects of cocaine. It has been proposed that the reinforcing properties of these conditional stimuli are due to their ability to elicit neural events that are similar to those produced by the drug itself. Given the large body of evidence that implicates the mesolimbic dopaminergic projection in the unconditioned behavioural properties of cocaine, the present study used in vivo microdialysis to determine whether stimuli paired with cocaine elicit increases in interstitial dopamine in the nucleus accumbens that are similar to the unconditioned effects of this drug. When administered acutely, cocaine (10 mg/kg, i.p.) produced a potent unconditioned increase in interstitial dopamine concentrations (300% of basal values) in the nucleus accumbens. The results from two separate experiments indicate that the administration of cocaine (10 mg/kg for seven days) in association with a specific environment produced significant locomotion in that environment. Compared to subjects that received saline in both settings, rats that received cocaine in their home cage (pseudoconditioned group) did not exhibit increased locomotion on the test day. Although repeated pairing of cocaine with a specific environment produced conditioned locomotion, there was no concomitant conditional increase in dopamine release. Specifically, the modest increase in dopamine (10-15% above basal values) observed after exposure to the conditional environment was equal in the conditioned and pseudoconditioned groups. Moreover, increases in the interstitial concentrations of the dopamine metabolites 3,4-dihydroxyphenylacetic acid and homovanillic acid were not significantly different between the conditioned and pseudoconditioned subjects. These data do not support the hypothesis that stimuli paired with cocaine produce their behavioural effects by eliciting similar neurochemical effects as cocaine.
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UNIV BRITISH COLUMBIA, FAC MED, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADAUNIV BRITISH COLUMBIA, FAC MED, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADA
BROWN, EE
FIBIGER, HC
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UNIV BRITISH COLUMBIA, FAC MED, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADAUNIV BRITISH COLUMBIA, FAC MED, DEPT PSYCHIAT, DIV NEUROL SCI, VANCOUVER V6T 1Z3, BC, CANADA
机构:
Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Radiol, Charlestown, MA 02129 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Ren, Jia-Qian
Jiang, Yan
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Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Radiol, Charlestown, MA 02129 USA
Beijing Univ Chinese Med, Dept Med, Beijing, Peoples R ChinaHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Jiang, Yan
Wang, Zhihui
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Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Radiol, Charlestown, MA 02129 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Wang, Zhihui
McCarthy, Deirdre
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Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
McCarthy, Deirdre
Rajadhyaksha, Anjali M.
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Cornell Univ, Weill Cornell Med Coll, Div Pediat Neurol, New York, NY 10021 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Rajadhyaksha, Anjali M.
Tropea, Thomas F.
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Cornell Univ, Weill Cornell Med Coll, Div Pediat Neurol, New York, NY 10021 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Tropea, Thomas F.
Kosofsky, Barry E.
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Cornell Univ, Weill Cornell Med Coll, Div Pediat Neurol, New York, NY 10021 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
Kosofsky, Barry E.
Bhide, Pradeep G.
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Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA