The Journal of Neuroscience, January 17, 2007, 27(3):553-563; doi:10.1523/JNEUROSCI.3686-06.2007
Previous Article | Next Article 
Cellular/Molecular
Networks of Parvalbumin-Positive Interneurons in the Basolateral Amygdala
Alan R. Woodruff and
Pankaj Sah
Queensland Brain Institute and School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia
Correspondence should be addressed to Pankaj Sah, Queensland Brain Institute, The University of Queensland, Brisbane, Queensland 4072, Australia. Email: pankaj.sah{at}uq.edu.au
The amygdala is a temporal lobe structure that is required for processing emotional information. Polymodal sensory information enters the amygdala at the level of the basolateral amygdala (BLA) and undergoes local processing, after which the behavioral and autonomic responses that accompany emotions are initiated. Two main neuron types are present in the BLA, pyramidal-like principal neurons that use glutamate as their transmitter, and local circuit interneurons that use GABA as their transmitter. Although the properties of principal neurons are known in some detail, very little is known about the properties of BLA interneurons or the local circuits in which they are involved. Using mice in which EGFP (enhanced green fluorescent protein) is expressed under the control of the parvalbumin promoter, we characterized the properties of parvalbumin-positive interneurons in the BLA. By making recordings from interneuroninterneuron and interneuronprincipal neuron pairs, we analyzed the intrinsic circuitry of the BLA. We show that parvalbumin-positive interneurons can be divided into four subtypes as defined by their firing properties. Interneurons are electrically coupled in subtype-specific networks and exhibit subtype-specific heterogeneities in their synaptic dynamics and patterns of connectivity. We propose that these properties allow networks of parvalbumin-expressing neurons to perform an array of information-processing tasks within the BLA.
Key words: oscillations; fear; network; fear; learning; LTP
Received Aug. 24, 2006;
revised Dec. 11, 2006;
accepted Dec. 12, 2006.
Correspondence should be addressed to Pankaj Sah, Queensland Brain Institute, The University of Queensland, Brisbane, Queensland 4072, Australia. Email: pankaj.sah{at}uq.edu.au
This article has been cited by other articles:

|
 |

|
 |
 
Y. Fu and V. Neugebauer
Differential Mechanisms of CRF1 and CRF2 Receptor Functions in the Amygdala in Pain-Related Synaptic Facilitation and Behavior
J. Neurosci.,
April 9, 2008;
28(15):
3861 - 3876.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Ji and V. Neugebauer
Pro- and Anti-Nociceptive Effects of Corticotropin-Releasing Factor (CRF) in Central Amygdala Neurons Are Mediated Through Different Receptors
J Neurophysiol,
March 1, 2008;
99(3):
1201 - 1212.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Geracitano, W. A. Kaufmann, G. Szabo, F. Ferraguti, and M. Capogna
Synaptic heterogeneity between mouse paracapsular intercalated neurons of the amygdala
J. Physiol.,
November 15, 2007;
585(1):
117 - 134.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. R. Woodruff and P. Sah
Inhibition and Synchronization of Basal Amygdala Principal Neuron Spiking by Parvalbumin-Positive Interneurons
J Neurophysiol,
November 1, 2007;
98(5):
2956 - 2961.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. P. Bauer, R. Paz, and D. Pare
Gamma Oscillations Coordinate Amygdalo-Rhinal Interactions during Learning
J. Neurosci.,
August 29, 2007;
27(35):
9369 - 9379.
[Abstract]
[Full Text]
[PDF]
|
 |
|