Literature DB >> 20129492

Cell death mechanisms and modulation in traumatic brain injury.

Bogdan A Stoica1, Alan I Faden.   

Abstract

Cell death after traumatic brain injury (TBI) is a major cause of neurological deficits and mortality. Understanding the mechanisms of delayed post-traumatic cell loss may lead to new therapies that improve outcome. Although TBI induces changes in multiple cell types, mechanisms of neuronal cell death have been the predominant focus. Recent work has emphasized the diversity of neuronal death phenotypes, which have generally been defined by either morphological or molecular changes. This diversity has led to confusing and at times contradictory nomenclature. Here we review the historical basis of proposed definitions of neuronal cell death, with the goal of clarifying critical research questions and implications for therapy in TBI. We believe that both morphological and molecular features must be used to clarify post-traumatic cell death and related therapeutic targets. Further, we underscore that the most effective neuroprotective strategies will need to target multiple pathways to reflect the regional and temporal changes underlying diverse neuronal cell death phenotypes. Copyright 2010 The American Society for Experimental NeuroTherapeutics, Inc. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20129492      PMCID: PMC2841970          DOI: 10.1016/j.nurt.2009.10.023

Source DB:  PubMed          Journal:  Neurotherapeutics        ISSN: 1878-7479            Impact factor:   7.620


  94 in total

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6.  Apoptosis-inducing factor triggered by poly(ADP-ribose) polymerase and Bid mediates neuronal cell death after oxygen-glucose deprivation and focal cerebral ischemia.

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9.  Influence of apoptosis on neurological outcome following traumatic cerebral contusion.

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  121 in total

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3.  A behavioral and histological comparison of fluid percussion injury and controlled cortical impact injury to the rat sensorimotor cortex.

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4.  Mild traumatic brain injury-induced hippocampal gene expressions: The identification of target cellular processes for drug development.

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5.  The expression patterns of Septin-9 after traumatic brain injury in rat brain.

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Journal:  J Mol Neurosci       Date:  2013-05-23       Impact factor: 3.444

6.  Strong Correlation of Genome-Wide Expression after Traumatic Brain Injury In Vitro and In Vivo Implicates a Role for SORLA.

Authors:  Michael R Lamprecht; Benjamin S Elkin; Kartik Kesavabhotla; John F Crary; Jennifer L Hammers; Jimmy W Huh; Ramesh Raghupathi; Barclay Morrison
Journal:  J Neurotrauma       Date:  2016-04-19       Impact factor: 5.269

7.  Incretin Mimetics as Rational Candidates for the Treatment of Traumatic Brain Injury.

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Journal:  ACS Pharmacol Transl Sci       Date:  2019-02-11

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Review 9.  ER stress and effects of DHA as an ER stress inhibitor.

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10.  Dynamic change of hydrogen sulfide after traumatic brain injury and its effect in mice.

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Journal:  Neurochem Res       Date:  2013-01-17       Impact factor: 3.996

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