catecholamine local circuit neocortex norepinephrine synaptic transmission
The noradrenergic system of the brain is thought to facilitate neuronal processes that promote behavioral activation, alertness, and attention. It is known that norepinephrine (NE) can be significantly elevated in the prefrontal cortex under normal conditions such as arousal and attention, and following administration of psychostimulants and various other drugs prescribed for psychiatric disorders. However, how NE modulates neuronal activity and synapses in the local prefrontal circuitry remains elusive. In this study, we characterized the actions of NE on individual monosynaptic connections among layer V pyramidal neurons (P) and fast-spiking (FS) GABAergic interneurons in the juvenile (postnatal days 20–23) rat prefrontal local circuitry. We found that NE selectively depresses excitatory synaptic transmission in P-FS connections but has no detectable effect on the excitatory synapses in P-P connections and the inhibitory synapses in FS-P connections. NE apparently exerts distinctly different modulatory actions on identified synapses that target GABAergic interneurons but has no effect on those in the pyramidal neurons in this specific developmental period. These results indicate that, depending on the postsynaptic targets, the effects of NE in prefrontal cortex are synapse-specific, at least in the juvenile animals.
Selective suppression of excitatory synapses on GABAergic interneurons by norepinephrine in juvenile rat prefrontal cortical microcircuitry
Creators
Huai-Xing Wang - Drexel University
Barry D. Waterhouse - Drexel University
Wen-Jun Gao - Drexel University
Publication Details
Neuroscience, v 246, pp 312-328
Publisher
Elsevier
Grant note
P50 MH068789 || MH / National Institute of Mental Health : NIMH
R01 MH085666 || MH / National Institute of Mental Health : NIMH
R21 MH079117 || MH / National Institute of Mental Health : NIMH
Resource Type
Journal article
Language
English
Academic Unit
Neurobiology and Anatomy; [Retired Faculty]
Web of Science ID
WOS:000321168000028
Scopus ID
2-s2.0-84878909611
Other Identifier
991019168200504721
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