TY - JOUR
T1 - Gait and conditioned fear impairments in a mouse model of comorbid TBI and PTSD
AU - Teutsch, Peyton
AU - Jones, Carolyn E.
AU - Kaiser, Mara E.
AU - Gardner, Natasha Avalon
AU - Lim, Miranda M.
N1 - Funding Information:
The authors would like to express their sincere appreciation and gratitude to Dr. Charles K. Meshul and Madeline L. Churchill for the use of the DigiGait apparatus, Delvin J. Akins for his input early on in establishing the combined TBI + PTSD protocol, Chau Nguyen for the assistance in video scoring, Ryan A. Opel for the surgical training, and the animal care staff in the Portland VA Veterinary Medical Unit. This material is the result of work supported with resources and the use of facilities at the VA Portland Health Care System, VA Career Development Award no. IK2 BX002712, NIH EXITO Institutional Core, no. UL1GM118964, the Oregon Medical Research Foundation New Investigator Award, and the Portland VA Research Foundation to Miranda M. Lim and NIH 5T32AA007468-29 and NIH 5T32HL083808-10 to Carolyn E. Jones.
Publisher Copyright:
© 2018 Peyton Teutsch et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2018
Y1 - 2018
N2 - Study Objectives: Traumatic brain injury (TBI) and posttraumatic stress disorder (PTSD) commonly cooccur. Approaches to research and treatment of these disorders have been segregated, despite overlapping symptomology. We and others have hypothesized that comorbid TBI + PTSD generates worse symptoms than either condition alone. We present a mouse model of comorbid TBI + PTSD to further explore this condition. Methods: A mouse model of TBI + PTSD was generated using the single prolonged stress (SPS) protocol in combination with the controlled cortical impact (CCI) protocol. This resulted in four experimental groups: control, TBI, PTSD, and TBI + PTSD. Behavioral phenotyping included gait analysis, contextual fear conditioning, acoustic startle response, and prepulse inhibition. Results: Mice in the TBI + PTSD group showed a significantly impaired gait compared to their counterparts with TBI alone as well as control mice. Mice in the TBI + PTSD group showed significantly impaired contextual fear recall compared to controls. Prepulse inhibition testing revealed intact acoustic startle and auditory sensory gating. Conclusions: These results indicate that SPS paired with CCI in mice produces unique behavioral impairments in gait and fear recall that are not present in either condition alone. Further studies are underway to examine additional behavioral, physiological, and pathological phenotypes in this combined model of TBI + PTSD.
AB - Study Objectives: Traumatic brain injury (TBI) and posttraumatic stress disorder (PTSD) commonly cooccur. Approaches to research and treatment of these disorders have been segregated, despite overlapping symptomology. We and others have hypothesized that comorbid TBI + PTSD generates worse symptoms than either condition alone. We present a mouse model of comorbid TBI + PTSD to further explore this condition. Methods: A mouse model of TBI + PTSD was generated using the single prolonged stress (SPS) protocol in combination with the controlled cortical impact (CCI) protocol. This resulted in four experimental groups: control, TBI, PTSD, and TBI + PTSD. Behavioral phenotyping included gait analysis, contextual fear conditioning, acoustic startle response, and prepulse inhibition. Results: Mice in the TBI + PTSD group showed a significantly impaired gait compared to their counterparts with TBI alone as well as control mice. Mice in the TBI + PTSD group showed significantly impaired contextual fear recall compared to controls. Prepulse inhibition testing revealed intact acoustic startle and auditory sensory gating. Conclusions: These results indicate that SPS paired with CCI in mice produces unique behavioral impairments in gait and fear recall that are not present in either condition alone. Further studies are underway to examine additional behavioral, physiological, and pathological phenotypes in this combined model of TBI + PTSD.
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U2 - 10.1155/2018/6037015
DO - 10.1155/2018/6037015
M3 - Article
C2 - 30327687
AN - SCOPUS:85055071977
SN - 0953-4180
VL - 2018
JO - Behavioural Neurology
JF - Behavioural Neurology
M1 - 6037015
ER -