WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (68)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chang, J.-Y.
Right arrow Articles by Woodward, D. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chang, J.-Y.
Right arrow Articles by Woodward, D. J.

 Previous Article

The Journal of Neuroscience, April 15, 1998, 18(8):3098-3115

Comparison of Mesocorticolimbic Neuronal Responses During Cocaine and Heroin Self-Administration in Freely Moving Rats

Jing-Yu Chang, Patricia H. Janak, and Donald J. Woodward

Department of Physiology and Pharmacology, Wake Forest University, School of Medicine, Winston-Salem, North Carolina 27157

To compare neuronal activity within the mesocorticolimbic circuit during the self-administration of cocaine and heroin, multiple-channel single-unit recordings of spike activity within the rat medial prefrontal cortex (mPFC) and nucleus accumbens (NAc) were obtained during the consecutive self-administration of cocaine and heroin within the same session. The variety of neuronal responses observed before the lever press are termed anticipatory responses, and those observed after the lever press are called post-drug infusion responses. For the total of the 110 mPFC and 111 NAc neurons recorded, 30-50% of neurons, depending on the individual sessions, had no alteration in spike activity in relation to either cocaine or heroin self-administration. Among the neurons exhibiting significant neuronal responses during a self-administration session, only a small portion (16-25%) of neurons responded similarly under both reinforcement conditions; the majority of neurons (75-84%) responded differently to cocaine and heroin self-administration as revealed by variations in both anticipatory and/or post-drug infusion responses. A detailed video analysis of specific movements to obtain the self-administration of both drugs provided evidence against the possibility that locomotive differences contributed to the observed differences in anticipatory responses. The overall mean activity of neurons recorded in mPFC and NAc measured across the duration of the session segment for either cocaine or heroin self-administration also was different for some neurons under the two reinforcement conditions. This study provides direct evidence that, in mPFC and NAc, heterogeneous neuronal circuits mediate cocaine and heroin self-administration and that distinct, but overlapping, subpopulations of neurons in these areas become active during operant responding for different reinforcers.

Key words: electrophysiology; cocaine; heroin; mesocorticolimbic system; medial prefrontal cortex; nucleus accumbens; reinforcement; reward; drug abuse; behavior


Copyright © 1998 Society for Neuroscience  0270-6474/98/1883098-18$05.00/0


This article has been cited by other articles:


Home page
J. Neurosci.Home page
E. H. Baeg, M. E. Jackson, H. P. Jedema, and C. W. Bradberry
Orbitofrontal and Anterior Cingulate Cortex Neurons Selectively Process Cocaine-Associated Environmental Cues in the Rhesus Monkey
J. Neurosci., September 16, 2009; 29(37): 11619 - 11627.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. Caille, L. Alvarez-Jaimes, I. Polis, D. G. Stouffer, and L. H. Parsons
Specific Alterations of Extracellular Endocannabinoid Levels in the Nucleus Accumbens by Ethanol, Heroin, and Cocaine Self-Administration
J. Neurosci., April 4, 2007; 27(14): 3695 - 3702.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
W. J. Kargo, B. Szatmary, and D. A. Nitz
Adaptation of Prefrontal Cortical Firing Patterns and Their Fidelity to Changes in Action-Reward Contingencies
J. Neurosci., March 28, 2007; 27(13): 3548 - 3559.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
P. W. German and H. L. Fields
Rat Nucleus Accumbens Neurons Persistently Encode Locations Associated With Morphine Reward
J Neurophysiol, March 1, 2007; 97(3): 2094 - 2106.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
D. R. Euston and B. L. McNaughton
Apparent Encoding of Sequential Context in Rat Medial Prefrontal Cortex Is Accounted for by Behavioral Variability
J. Neurosci., December 20, 2006; 26(51): 13143 - 13155.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. I. G. Wilson and E. M. Bowman
Rat Nucleus Accumbens Neurons Predominantly Respond to the Outcome-Related Properties of Conditioned Stimuli Rather Than Their Behavioral-Switching Properties
J Neurophysiol, July 1, 2005; 94(1): 49 - 61.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
S. M. Nicola, I. A. Yun, K. T. Wakabayashi, and H. L. Fields
Cue-Evoked Firing of Nucleus Accumbens Neurons Encodes Motivational Significance During a Discriminative Stimulus Task
J Neurophysiol, April 1, 2004; 91(4): 1840 - 1865.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
S. M. Nicola, I. A. Yun, K. T. Wakabayashi, and H. L. Fields
Firing of Nucleus Accumbens Neurons During the Consummatory Phase of a Discriminative Stimulus Task Depends on Previous Reward Predictive Cues
J Neurophysiol, April 1, 2004; 91(4): 1866 - 1882.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. M. Carelli and J. Wondolowski
Selective Encoding of Cocaine versus Natural Rewards by Nucleus Accumbens Neurons Is Not Related to Chronic Drug Exposure
J. Neurosci., December 3, 2003; 23(35): 11214 - 11223.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. L. Peoples and D. Cavanaugh
Differential Changes in Signal and Background Firing of Accumbal Neurons During Cocaine Self-Administration
J Neurophysiol, August 1, 2003; 90(2): 993 - 1010.
[Abstract] [Full Text] [PDF]


Home page
Behav Cogn Neurosci RevHome page
R. M. Carelli
The nucleus accumbens and reward: neurophysiological investigations in behaving animals.
Behav Cogn Neurosci Rev, December 1, 2002; 1(4): 281 - 296.
[Abstract] [PDF]


Home page
J. Neurosci.Home page
T. J. De Vries and T. S. Shippenberg
Neural Systems Underlying Opiate Addiction
J. Neurosci., May 1, 2002; 22(9): 3321 - 3325.
[Full Text] [PDF]


Home page
Physiol. Rev.Home page
J. T. Williams, M. J. Christie, and O. Manzoni
Cellular and Synaptic Adaptations Mediating Opioid Dependence
Physiol Rev, January 1, 2001; 81(1): 299 - 343.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. M. Carelli, S. G. Ijames, and A. J. Crumling
Evidence That Separate Neural Circuits in the Nucleus Accumbens Encode Cocaine Versus "Natural" (Water and Food) Reward
J. Neurosci., June 1, 2000; 20(11): 4255 - 4266.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. L. Peoples, F. Gee, R. Bibi, and M. O. West
Phasic Firing Time Locked to Cocaine Self-Infusion and Locomotion: Dissociable Firing Patterns of Single Nucleus Accumbens Neurons in the Rat
J. Neurosci., September 15, 1998; 18(18): 7588 - 7598.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-