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      Limbic Responses Following Shock Wave Exposure in Male and Female Mice

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          Abstract

          Blast traumatic brain injury (bTBI) presents a serious threat to military personnel and often results in psychiatric conditions related to limbic system dysfunction. In this study, the functional outcomes for anxiety- and depressive-like behaviors and neuronal activation were evaluated in male and female mice after exposure to an Advanced Blast Simulator (ABS) shock wave. Mice were placed in a ventrally exposed orientation inside of the ABS test section and received primary and tertiary shock wave insults of approximately 15 psi peak pressure. Evans blue staining indicated cases of blood-brain barrier breach in the superficial cerebral cortex four, but not 24 h after blast, but the severity was variable. Behavioral testing with the elevated plus maze (EPM) or elevated zero maze (EZM), sucrose preference test (SPT), and tail suspension test (TST) or forced swim test (FST) were conducted 8 days–3.5 weeks after shock wave exposure. There was a sex difference, but no injury effect, for distance travelled in the EZM where female mice travelled significantly farther than males. The SPT and FST did not indicate group differences; however, injured mice were less immobile than sham mice during the TST; possibly indicating more agitated behavior. In a separate cohort of animals, the expression of the immediate early gene, c-Fos, was detected 4 h after undergoing bTBI or sham procedures. No differences in c-Fos expression were found in the cerebral cortex, but female mice in general displayed enhanced c-Fos activation in the paraventricular nucleus of the thalamus (PVT) compared to male mice. In the amygdala, more c-Fos-positive cells were observed in injured animals compared to sham mice. The observed sex differences in the PVT and c-Fos activation in the amygdala may correlate with the reported hyperactivity of females post-injury. This study demonstrates, albeit with mild effects, behavioral and neuronal activation correlates in female rodents after blast injury that could be relevant to the incidence of increased post-traumatic stress disorder in women.

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          Most cited references85

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          Depression: a new animal model sensitive to antidepressant treatments.

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            Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat.

            A novel test for the selective identification of anxiolytic and anxiogenic drug effects in the rat is described, using an elevated + -maze consisting of two open arms and two enclosed arms. The use of this test for detecting such drug effects was validated behaviourally, physiologically, and pharmacologically. Rats made significantly fewer entries into the open arms than into the closed arms, and spent significantly less time in open arms. Confinement to the open arms was associated with the observation of significantly more anxiety-related behaviours, and of significantly greater plasma corticosterone concentrations, than confinement to the closed arms. Neither novelty nor illumination was a significant contributor to the behaviour of the rats on the + -maze. A significant increase in the percentage of time spent on the open arms and the number of entries into the open arms was observed only within clinically effective anxiolytics (chlordiazepoxide, diazepam and, less effectively, phenobarbitone). Compounds that cause anxiety in man significantly reduced the percentage of entries into, and time spent on, the open arms (yohimbine, pentylenetetrazole, caffeine, amphetamine). Neither antidepressants nor major tranquilisers had a specific effect. Exposure to a holeboard immediately before placement on the + -maze showed that behaviour on the maze was not clearly correlated either with exploratory head-dipping or spontaneous locomotor activity.
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              Placing the paraventricular nucleus of the thalamus within the brain circuits that control behavior.

              This article reviews the anatomical connections of the paraventricular nucleus of the thalamus (PVT) and discusses some of the connections by which the PVT could influence behavior. The PVT receives neurochemically diverse projections from the brainstem and hypothalamus with an especially strong innervation from peptide producing neurons. Anatomical evidence is also presented which suggests that the PVT relays information from neurons involved in visceral or homeostatic functions. In turn, the PVT is a major source of projections to the nucleus accumbens, the bed nucleus of the stria terminalis and the central nucleus of the amygdala as well as the cortical areas associated with these subcortical regions. The PVT is activated by conditions and cues that produce states of arousal including those with appetitive or aversive emotional valences. The paper focuses on the potential contribution of the PVT to circadian rhythms, fear, anxiety, food intake and drug-seeking. The information in this paper highlights the potential importance of the PVT as being a component of the brain circuits that regulate reward and defensive behavior with the hope of generating more research in this relatively understudied region of the brain.
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                Author and article information

                Contributors
                Journal
                Front Behav Neurosci
                Front Behav Neurosci
                Front. Behav. Neurosci.
                Frontiers in Behavioral Neuroscience
                Frontiers Media S.A.
                1662-5153
                07 June 2022
                2022
                : 16
                : 863195
                Affiliations
                [1] 1Department of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences , Bethesda, MD, United States
                [2] 2Pre-Clinical Studies Core, Center for Neuroscience and Regenerative Medicine, Henry M. Jackson Foundation , Bethesda, MD, United States
                Author notes

                Edited by: Matthew J. Robson, University of Cincinnati, United States

                Reviewed by: Abigail Grace Schindler, University of Washington, United States; Christopher Olsen, Medical College of Wisconsin, United States

                *Correspondence: Joseph T. McCabe, Joseph.McCabe@ 123456usuhs.edu

                This article was submitted to Behavioral Endocrinology, a section of the journal Frontiers in Behavioral Neuroscience

                Article
                10.3389/fnbeh.2022.863195
                9210954
                35747840
                e0b752c8-9dc2-4f81-9d06-c896ccf63b56
                Copyright © 2022 McNamara, Tucker, Liu, Fu, Kim, Vu and McCabe.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 26 January 2022
                : 04 April 2022
                Page count
                Figures: 8, Tables: 0, Equations: 1, References: 86, Pages: 14, Words: 11075
                Funding
                Funded by: Center for Neuroscience and Regenerative Medicine, doi 10.13039/100013130;
                Categories
                Neuroscience
                Original Research

                Neurosciences
                anxiety,blood-brain barrier,c-fos,depression,limbic,post-traumatic stress disorder,blast traumatic brain injury (btbi),righting reflex

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