Anna Oleshko, Benjamin F Gruenbaum, Vladislav Zvenigorodsky, Ilan Shelef, Shahar Negev, Igor Merzlikin, Israel Melamed, Alexander Zlotnik, Amit Frenkel, Matthew Boyko
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引用次数: 0
Abstract
Traumatic brain injury (TBI) is a significant global health concern and is associated with short-term and long-term comorbidities such as mood disorders and reduced quality of life. Diffuse axonal brain injury (DABI) is a common but severe type of TBI. The role of DABI in the development of psychiatric sequelae after TBI is not well understood due to the challenge of isolating DABI from general TBI in the human population. Here we investigate the role of DABI in the occurrence of post-TBI depressive- and anxiety-like behaviors in a rat model. Forty rats were randomly assigned to two groups, with 20 receiving DABI and 20 receiving sham treatment. We used a magnetic resonance imaging (MRI) protocol developed for DABI using a 3-T clinical scanner to confirm DABI. We then compared neuroimaging, neurological and behavioral assessments across experimental groups. There was a significant difference between DABI and sham groups on sucrose preference, a measurement of depressive-like behavior (p < 0.012), and time spent on open arms on a plus maze test, a measurement of anxiety-like behavior (p < 0.032). For MRI-detected injury, there was a difference in diffusion-weighted imaging with relative anisotropy (p < 0.001) and fractional anisotropy (p < 0.001) mapping. We found that isolated DABI in our model led to post-traumatic depressive-like behavior in 30% of cases and anxiety-like behavior in 35%. Additionally, we established diagnostic cut-offs for depressive-like and anxiety-like behaviors in injured rats. We also documented comorbidity between the development of depression and anxiety in DABI-exposed rats. We anticipate that this study will greatly enhance the understanding of the relationship between DABI, TBI, and mood disorders like depression and anxiety, and aid in developing treatment options for these interconnected conditions.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.