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Trace Fear Conditioning in Mice
Published on: March 20, 2014
MR diffusion tensor imaging detects rapid microstructural changes in amygdala and hippocampus following fear
Abby Y Ding1, Qi Li, Iris Y Zhou
1Laboratory of Biomedical Imaging and Signal Processing, The University of Hong Kong, Hong Kong SAR, China.
Plos One
|February 6, 2013
Summary
Diffusion tensor imaging (DTI) detects rapid, in vivo microstructural brain changes after fear conditioning (FC). These early changes in the amygdala and hippocampus may offer insights into anxiety disorders like posttraumatic stress disorder (PTSD).
Area of Science:
- Neuroscience
- Neuroimaging
- Brain Plasticity
Background:
- Fear conditioning (FC) involves cellular and molecular plasticity in amygdala and hippocampal circuits.
- Altered fear circuit dynamics are linked to anxiety disorders, including posttraumatic stress disorder (PTSD).
- In vivo evidence of early fear circuit changes following FC is currently unknown.
Purpose of the Study:
- To investigate if in vivo diffusion tensor imaging (DTI) can detect rapid microstructural changes after fear conditioning (FC).
- To establish an experimental mouse model for studying PTSD-related brain alterations.
- To compare DTI measurements before and after FC in mice.
Main Methods:
- Utilized a repeated measures design with in vivo DTI.
- Measured DTI parameters in mice (n=18) before, 1 hour after, and 1 day after FC.
- Employed voxel-wise repeated measures analysis to assess changes in fractional anisotropy (FA).
Main Results:
- Fractional anisotropy (FA) showed significant changes in the amygdala and hippocampus post-FC.
- FA increased then decreased in the amygdala, and decreased then increased in the hippocampus.
- DTI revealed distinct, rapid in vivo microstructural responses in fear circuits following FC.
Conclusions:
- DTI is sensitive to rapid, in vivo microstructural changes in brain regions mediating FC.
- FC elicits distinct and rapid in vivo responses in the amygdala and hippocampus.
- DTI indices show potential as a translational tool for early PTSD risk detection.

