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Gait and Conditioned Fear Impairments in Mouse Model of Comorbid TBI and PTSD
被引:15
|作者:
Teutsch, Peyton
[1
]
Jones, Carolyn E.
[1
,2
]
Kaiser, Mara E.
[1
]
Gardner, Natasha Avalon
[1
,3
]
Lim, Miranda M.
[1
,2
,4
]
机构:
[1] VA Portland Hlth Care Syst, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97201 USA
[3] Portland State Univ, Portland, OR 97207 USA
[4] Oregon Hlth & Sci Univ, Dept Med, Oregon Inst Occupat Hlth Sci, Dept Neurol,Div Pulm & Crit Care Med, Portland, OR 97201 USA
关键词:
TRAUMATIC BRAIN-INJURY;
PREPULSE INHIBITION;
STRESS;
IMPACT;
DEFICITS;
MILD;
D O I:
10.1155/2018/6037015
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
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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