Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/29094
Title: Adolescents are more vulnerable to cocaine addiction : behavioral and electrophysiological evidence
Authors: Wong, Wai Chong
Ford, Kerstin A.
Pagels, Nicole E.
McCutcheon, James E.
Marinelli, Michela
First Published: 13-Mar-2013
Publisher: Society for Neuroscience
Citation: Journal of Neuroscience, 2013, 33 (11), pp. 4913-4922
Abstract: In humans, adolescence is a period of heightened propensity to develop cocaine addiction. It is unknown whether this is attributable to greater access and exposure to cocaine at this age, or whether the adolescent brain is particularly vulnerable to the addictive properties of cocaine. Here, we subjected male adolescent (P42) and adult (∼P88) rats to a wide range of cocaine self-administration procedures. In addition, to determine whether behavioral differences are associated with developmental differences in dopaminergic activity, we examined and manipulated the activity of dopamine neurons. Relative to adults, adolescent rats took cocaine more readily, were more sensitive to lower doses, showed greater escalation of cocaine intake, and were less susceptible to increases in price (i.e., were more “inelastic”). In parallel, adolescents also showed elevated activity of ventral tegmental area dopamine neurons, a feature known to be associated with increased self-administration behavior. Pharmacological manipulation of dopamine D2 receptor function with quinpirole (agonist) or eticlopride (antagonist), to alter dopamine neuron activity, eliminated age differences in cocaine self-administration. These data suggest a causal relationship between behavioral and electrophysiological determinants of cocaine addiction liability. In conclusion, adolescents show behavioral and electrophysiological traits of heightened addiction liability.
DOI Link: 10.1523/JNEUROSCI.1371-12.2013
ISSN: 0270-6474
eISSN: 1529-2401
Links: http://www.jneurosci.org/content/33/11/4913
http://hdl.handle.net/2381/29094
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © 2013, Society for Neuroscience. Deposited with reference to the publisher’s archiving policy available on the SHERPA/RoMEO website.
Appears in Collections:Published Articles, Dept. of Cell Physiology and Pharmacology

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