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Hemodynamic responses in amygdala and hippocampus distinguish between aversive and neutral cues during Pavlovian fear conditioning in behaving rats

Abstract:
Amygdala and hippocampal tissue oxygen (TO2) signals were recorded from freely-moving rats during discriminative Pavlovian fear conditioning. TO2 signals provide a close surrogate for the BOLD-fMRI signal. TO2 signals in both regions discriminated between conditioned aversive (CS+) and neutral (CS-) cues. These data challenge recent claims that hemodynamic signals cannot detect the different patterns of neuronal activity evoked by CS+ vs. CS- stimuli. Lesion and electrophysiological studies in rodents have identified the amygdala and hippocampus (HPC) as key structures for Pavlovian fear conditioning, but human functional neuroimaging studies have not consistently found activation of these structures. This could be because hemodynamic responses cannot detect the sparse neuronal activity proposed to underlie conditioned fear. Alternatively, differences in experimental design or fear levels could account for the discrepant findings between rodents and humans. To help distinguish between these alternatives, we used tissue oxygen amperometry to record hemodynamic responses from the basolateral amygdala (BLA), dorsal HPC (dHPC) and ventral HPC (vHPC) in freely-moving rats during the acquisition and extinction of conditioned fear. To enable specific comparison with human studies we used a discriminative paradigm, with one auditory cue [conditioned stimulus (CS)+] that was always followed by footshock, and another auditory cue (CS-) that was never followed by footshock. BLA tissue oxygen signals were significantly higher during CS+ than CS- trials during training and early extinction. In contrast, they were lower during CS+ than CS- trials by the end of extinction. dHPC and vHPC tissue oxygen signals were significantly lower during CS+ than CS- trials throughout extinction. Thus, hemodynamic signals in the amygdala and HPC can detect the different patterns of neuronal activity evoked by threatening vs. neutral stimuli during fear conditioning. Discrepant neuroimaging findings may be due to differences in experimental design and/or fear levels evoked in participants. Our methodology offers a way to improve translation between rodent models and human neuroimaging. © 2012 Federation of European Neuroscience Societies and Blackwell Publishing Ltd.

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Publisher copy:
10.1111/ejn.12057

Authors



Journal:
European Journal of Neuroscience More from this journal
Volume:
37
Issue:
3
Pages:
498-507
Publication date:
2013-02-01
DOI:
EISSN:
1460-9568
ISSN:
0953-816X


Language:
English
Keywords:
Pubs id:
pubs:384997
UUID:
uuid:defc2290-23d8-4c48-afd7-685ceb278518
Local pid:
pubs:384997
Source identifiers:
384997
Deposit date:
2013-11-16

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