Dissociable contributions of the amygdala and ventral hippocampus to stress-induced changes in defensive behavior
Pennington ZT, LaBanca AR, Sompolpong P, Christenson Wick Z, Feng Y, Francisco TR, Chen L, Fulton SL, Maze I, Dong Z, Cai DJ (2023)
Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai
All data and analysis are available here for reproduction and further analysis.
All analysis were conducted using RStudio, using the following packages: ggplot2, ez, tidyr, dplyr, purrr, lmtest, car, knitr.
Each experimental folder has a single analysis file (.rmd). When the working directory is set to .rmd location, file can be run to load in all experimental data and reproduce analysis/plots.
A brief description of each experiment is provided below.
For each figure, we highlight the respective experiments included.
List of experiments in each figure
- 1c1d (panels B-E)
- 10j10e3 (panels F-H)
- 10g2g3 (panels B-E)
- 10j10e3 (panels F-J)
- 10k6 (panels A, F-J)
- 10k9 (panels B)
- 10k6c (panels C-E)
- 10n5b (all panels)
- 1c1d (all panels)
- 1f (all panels)
- 10j10e3 (all panels)
- 10j10e3 (all panels)
- 10e (all panels)
- 10e (all panels)
- 10k6 (all panels)
- 10k5 (panels B-C)
- 10k (panels E-H)
- 10k6b (panels B-D)
- 10k2 (panels E-F)
A very brief description of experiments. See manuscript for details.
Basic behavioral effects showing influence of initial stressor/trauma is amplitude dependent and not influenced by sex
Learning rate analysis
Exps demonstrating anisomycin in amygdala blocks learning without altering expression, and also blocks IEG protein expression.
Anisomycin given systemically after trauma. A week later, animals tested in light-dark test, trauma memory recall, and novel stressor and subsequent novel stressor recall. Note that although this experiment includes animals given anisomycin either 2 or 3 times after trauma, only animals receiving 3 injections of anisomycin are included in manuscript.
Anisomycin in either the BLA (10e3) or vHC (10j) just after trauma. A week later, animals tested in light-dark test, trauma memory recall, and novel stressor test and subsequent novel stressor recall. Additionally, controls from these experiemnts given vehicle were utilized to show normative effects and relationships between phenotypes. For main analysis, controls with vehicle in vHC or BLA were collapsed after being shown to not be different.
Effect of inhibiting either BLA or vHC on light-dark test and novel stressor using PSAM.
Effect of inhibiting either BLA or vHC on light-dark, open field, and elevated plus maze tests using PSAM.
Effect of inhibiting either BLA or vHC during trauma memory recall using PSAM. Note animals also received uPSEM or vehicle with novel stressor at end of experiment (currently low N).
Effect of inhibiting either BLA or vHC on light-dark test and novel stressor using HM4D.
Effect of inhibiting either BLA or vHC on light-dark, open field, and elevated plus maze tests using HM4D.
Effect of inhibiting either BLA or vHC on fear memory recall.
Validation of HM4Di-mediated inhbition of BLA/vHC with in slice.
Inhibition of BLA->vHC and vHC->BLA projections on light-dark test and novel stressor using HM4D.