 |
The Journal of Neuroscience, April 6, 2005, 25(14):3674-3679; doi:10.1523/JNEUROSCI.0010-05.2005
Previous Article | Next Article 
BRIEF COMMUNICATION
Repeated Cocaine Administration Increases Voltage-Sensitive Calcium Currents in Response to Membrane Depolarization in Medial Prefrontal Cortex Pyramidal Neurons
Fernando J. Nasif,
Xiu-Ti Hu, and
Francis J. White
Department of Cellular and Molecular Pharmacology, Rosalind Franklin University of Medicine and Science, The Chicago Medical School, North Chicago, Illinois 60064
The medial prefrontal cortex (mPFC) plays a critical role in cocaine addiction. However, evidence to elucidate how the mPFC is functionally involved in cocaine addiction remains incomplete. Recent studies have revealed that repeated cocaine administration induces various neuroadaptations in pyramidal mPFC neurons, including a reduction in voltage-gated K+ currents (VGKCs) and a possible increase in voltage-sensitive Ca2+ currents (ICa). Here, we performed both current-clamp recordings in brain slices and voltage-clamp recordings in freshly dissociated cells to determine whether ICa is altered in mPFC pyramidal neurons after chronic cocaine treatment with a short-term or long-term withdrawal. In addition, a critical role of VGKCs in regulating the generation of Ca2+ plateau potential was also studied in mPFC neurons. Repeated cocaine administration significantly prolonged the duration of evoked Ca2+ plateau potentials and increased the whole-cell ICa in mPFC neurons after a 3 d withdrawal. Selective blockade of L-type Ca2+ channels by nifedipine not only significantly increased the threshold but also reduced the duration and amplitude of Ca2+ plateau potentials in both saline- and cocaine-withdrawn mPFC neurons. However, there was no significant difference in the increased threshold, reduced duration, and decreased amplitude of Ca2+ potentials between saline- and cocaine-withdrawn neurons after blockade of L-type Ca2+ channels. Moreover, an increase in amplitude was also observed, whereas the prolonged duration persisted, in Ca2+ potentials after 2-3 weeks of withdrawal. These findings indicate that chronic exposure to cocaine facilitates the responsiveness of ICa, particularly via the activated L-type Ca2+ channels, to excitatory stimuli in rat mPFC pyramidal neurons.
Key words: cocaine; medial prefrontal cortex; psychostimulant; Ca2+ current; Ca2+ plateau potential; patch clamp
Received Jan 3, 2005;
revised February 15, 2005;
accepted March 3, 2005.
This article has been cited by other articles:

|
 |

|
 |
 
H. Lu, B. Lim, and M.-m. Poo
Cocaine Exposure In Utero Alters Synaptic Plasticity in the Medial Prefrontal Cortex of Postnatal Rats
J. Neurosci.,
October 7, 2009;
29(40):
12664 - 12674.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Orozco-Cabal, J. Liu, S. Pollandt, K. Schmidt, P. Shinnick-Gallagher, and J. P. Gallagher
Dopamine and Corticotropin-Releasing Factor Synergistically Alter Basolateral Amygdala-to-Medial Prefrontal Cortex Synaptic Transmission: Functional Switch after Chronic Cocaine Administration
J. Neurosci.,
January 9, 2008;
28(2):
529 - 542.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. C. Rotaru, D. A. Lewis, and G. Gonzalez-Burgos
Dopamine D1 receptor activation regulates sodium channel-dependent EPSP amplification in rat prefrontal cortex pyramidal neurons
J. Physiol.,
June 15, 2007;
581(3):
981 - 1000.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
I. Calin-Jageman, K. Yu, R. A. Hall, L. Mei, and A. Lee
Erbin Enhances Voltage-Dependent Facilitation of Cav1.3 Ca2+ Channels through Relief of an Autoinhibitory Domain in the Cav1.3 {alpha}1 Subunit
J. Neurosci.,
February 7, 2007;
27(6):
1374 - 1385.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Fu, S. Pollandt, J. Liu, B. Krishnan, K. Genzer, L. Orozco-Cabal, J. P. Gallagher, and P. Shinnick-Gallagher
Long-Term Potentiation (LTP) in the Central Amygdala (CeA) Is Enhanced After Prolonged Withdrawal From Chronic Cocaine and Requires CRF1 Receptors
J Neurophysiol,
January 1, 2007;
97(1):
937 - 941.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Cormaci, T. Mori, T. Hayashi, and T.-P. Su
Protein Kinase A Activation Down-Regulates, Whereas Extracellular Signal-Regulated Kinase Activation Up-Regulates {sigma}-1 Receptors in B-104 Cells: Implication for Neuroplasticity
J. Pharmacol. Exp. Ther.,
January 1, 2007;
320(1):
202 - 210.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Nogueira, P. W. Kalivas, and A. Lavin
Long-Term Neuroadaptations Produced by Withdrawal from Repeated Cocaine Treatment: Role of Dopaminergic Receptors in Modulating Cortical Excitability.
J. Neurosci.,
November 22, 2006;
26(47):
12308 - 12313.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Du, M. Yu, N. D. Volkow, A. P. Koretsky, J. S. Fowler, and H. Benveniste
Cocaine Increases the Intracellular Calcium Concentration in Brain Independently of Its Cerebrovascular Effects.
J. Neurosci.,
November 8, 2006;
26(45):
11522 - 11531.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. Sun and G. V. Rebec
Repeated cocaine self-administration alters processing of cocaine-related information in rat prefrontal cortex.
J. Neurosci.,
July 26, 2006;
26(30):
8004 - 8008.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|