3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Investigation of the direct and indirect mechanisms of primary blast insult to the brain

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The interaction of explosion-induced blast waves with the head (i.e., a direct mechanism) or with the torso (i.e., an indirect mechanism) presumably causes traumatic brain injury. However, the understanding of the potential role of each mechanism in causing this injury is still limited. To address this knowledge gap, we characterized the changes in the brain tissue of rats resulting from the direct and indirect mechanisms at 24 h following blast exposure. To this end, we conducted separate blast-wave exposures on rats in a shock tube at an incident overpressure of 130 kPa, while using whole-body, head-only, and torso-only configurations to delineate each mechanism. Then, we performed histopathological (silver staining) and immunohistochemical (GFAP, Iba-1, and NeuN staining) analyses to evaluate brain-tissue changes resulting from each mechanism. Compared to controls, our results showed no significant changes in torso-only-exposed rats. In contrast, we observed significant changes in whole-body-exposed (GFAP and silver staining) and head-only-exposed rats (silver staining). In addition, our analyses showed that a head-only exposure causes changes similar to those observed for a whole-body exposure, provided the exposure conditions are similar. In conclusion, our results suggest that the direct mechanism is the major contributor to blast-induced changes in brain tissues.

          Related collections

          Most cited references43

          • Record: found
          • Abstract: not found
          • Article: not found

          Fitting Linear Mixed-Effects Models Usinglme4

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Astrocytes: biology and pathology

            Astrocytes are specialized glial cells that outnumber neurons by over fivefold. They contiguously tile the entire central nervous system (CNS) and exert many essential complex functions in the healthy CNS. Astrocytes respond to all forms of CNS insults through a process referred to as reactive astrogliosis, which has become a pathological hallmark of CNS structural lesions. Substantial progress has been made recently in determining functions and mechanisms of reactive astrogliosis and in identifying roles of astrocytes in CNS disorders and pathologies. A vast molecular arsenal at the disposal of reactive astrocytes is being defined. Transgenic mouse models are dissecting specific aspects of reactive astrocytosis and glial scar formation in vivo. Astrocyte involvement in specific clinicopathological entities is being defined. It is now clear that reactive astrogliosis is not a simple all-or-none phenomenon but is a finely gradated continuum of changes that occur in context-dependent manners regulated by specific signaling events. These changes range from reversible alterations in gene expression and cell hypertrophy with preservation of cellular domains and tissue structure, to long-lasting scar formation with rearrangement of tissue structure. Increasing evidence points towards the potential of reactive astrogliosis to play either primary or contributing roles in CNS disorders via loss of normal astrocyte functions or gain of abnormal effects. This article reviews (1) astrocyte functions in healthy CNS, (2) mechanisms and functions of reactive astrogliosis and glial scar formation, and (3) ways in which reactive astrocytes may cause or contribute to specific CNS disorders and lesions.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Molecular dissection of reactive astrogliosis and glial scar formation.

              Reactive astrogliosis, whereby astrocytes undergo varying molecular and morphological changes, is a ubiquitous but poorly understood hallmark of all central nervous system pathologies. Genetic tools are now enabling the molecular dissection of the functions and mechanisms of reactive astrogliosis in vivo. Recent studies provide compelling evidence that reactive astrogliosis can exert both beneficial and detrimental effects in a context-dependent manner determined by specific molecular signaling cascades. Reactive astrocytes can have both loss of normal functions and gain of abnormal effects that could feature prominently in a variety of disease processes. This article reviews developments in the signaling mechanisms that regulate specific aspects of reactive astrogliosis and highlights the potential to identify novel therapeutic molecular targets for diverse neurological disorders.
                Bookmark

                Author and article information

                Contributors
                jaques.reifman.civ@mail.mil
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                6 August 2021
                6 August 2021
                2021
                : 11
                : 16040
                Affiliations
                [1 ]GRID grid.420210.5, ISNI 0000 0001 0036 4726, Department of Defense Biotechnology High Performance Computing Software Applications Institute, Telemedicine and Advanced Technology Research Center, , United States Army Medical Research and Development Command, ; ATTN: FCMR-TT, 504 Scott Street, Fort Detrick, MD 21702-5012 USA
                [2 ]GRID grid.201075.1, ISNI 0000 0004 0614 9826, The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., ; 6720A Rockledge Drive, Bethesda, MD 20817 USA
                [3 ]GRID grid.507680.c, ISNI 0000 0001 2230 3166, Blast Induced Neurotrauma Division, Center for Military Psychiatry and Neurosciences, , Walter Reed Army Institute of Research, ; 503 Robert Grant Drive, Silver Spring, MD 20910 USA
                [4 ]GRID grid.260896.3, ISNI 0000 0001 2166 4955, Department of Biomedical Engineering, Center for Injury Biomechanics, Materials, and Medicine, , New Jersey Institute of Technology, ; 111 Lock Street, Newark, NJ 07103 USA
                Article
                95003
                10.1038/s41598-021-95003-9
                8346555
                34362935
                5a0caee1-504f-4249-a3c9-a826e56bc3fc
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 3 May 2021
                : 12 July 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100016156, U.S. Army Medical Research and Development Command;
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award ID: W81XWH20C0031
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                neuroscience,brain injuries
                Uncategorized
                neuroscience, brain injuries

                Comments

                Comment on this article