Literature DB >> 8863193

Secondary insults increase injury after controlled cortical impact in rats.

L Cherian1, C S Robertson, J C Goodman.   

Abstract

Secondary ischemic insults are common after severe head injury and contribute to poor neurological outcome. To study the increased vulnerability of the traumatized brain to secondary insults, bilateral carotid occlusion was produced after a controlled cortical impact injury in rats. The injury produced by either the impact injury or the bilateral carotid occlusion was mild to moderate when studied individually. The 1 and 3 m/sec impact injuries alone caused no detectable contusion at the impact side and minimal neuronal loss in the hippocampus. The 5 m/sec impact injury alone resulted in a small contusion with a median volume of 5.4 mm3. The 40-min period of bilateral carotid occlusion alone caused no cortical injury and no neuronal loss in the CA1 region of the hippocampus. When the 40 min of bilateral carotid occlusion was produced 1 h after the impact injury, there was an increase in the damage produced. The contusion volume was significantly larger after the 3 and 5 m/sec impact injuries and the hippocampal neuronal loss was significantly greater after the 1 and 3 m/sec impact injuries. When varying durations of bilateral carotid occlusion were produced 1 h after a 3 m/sec impact injury, contusion volume was significantly larger after bilateral carotid occlusion duration of 40 min, and CA1 neuronal loss was significantly greater after bilateral carotid occlusion durations of 30 and 40 min. When 40 min of bilateral carotid occlusion was produced at different time intervals after a 3 m/sec injury, the increased contusion volume was maximal when bilateral carotid occlusion occurred at 4 h after the impact injury, and the increased neuronal loss in the CA3 region of the hippocampus was maximal when bilateral carotid occlusion occurred at 1 h after the impact injury. By 24 h after the impact injury, 40 min of bilateral carotid occlusion had minimal consequences, similar to the effect in sham-injured animals. These results mimic the clinical situation where secondary insults of a severity that would not cause permanent neurological damage in a normal person are associated with a marked worsening of neurological outcome after head injury and where the injured brain is most susceptible to secondary insults in the first few hours after injury.

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Year:  1996        PMID: 8863193     DOI: 10.1089/neu.1996.13.371

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  12 in total

1.  Severe brief pressure-controlled hemorrhagic shock after traumatic brain injury exacerbates functional deficits and long-term neuropathological damage in mice.

Authors:  Joseph N Hemerka; Xianren Wu; C Edward Dixon; Robert H Garman; Jennifer L Exo; David K Shellington; Brian Blasiole; Vincent A Vagni; Keri Janesko-Feldman; Mu Xu; Stephen R Wisniewski; Hülya Bayır; Larry W Jenkins; Robert S B Clark; Samuel A Tisherman; Patrick M Kochanek
Journal:  J Neurotrauma       Date:  2012-08-10       Impact factor: 5.269

2.  Effects of trauma, hemorrhage and resuscitation in aged rats.

Authors:  Bridget E Hawkins; Jeremy C Cowart; Margaret A Parsley; Bridget A Capra; Kristine A Eidson; Helen L Hellmich; Douglas S Dewitt; Donald S Prough
Journal:  Brain Res       Date:  2012-12-28       Impact factor: 3.252

3.  Astrocyte activation and wound healing in intact-skull mouse after focal brain injury.

Authors:  Takayuki Suzuki; Honami Sakata; Chiaki Kato; John A Connor; Mitsuhiro Morita
Journal:  Eur J Neurosci       Date:  2012-09-27       Impact factor: 3.386

4.  Neuroprotection with an erythropoietin mimetic peptide (pHBSP) in a model of mild traumatic brain injury complicated by hemorrhagic shock.

Authors:  Claudia S Robertson; Leela Cherian; Mahek Shah; Robert Garcia; Jovany Cruz Navarro; Raymond J Grill; Carla Cerami Hand; Tian Siva Tian; H Julia Hannay
Journal:  J Neurotrauma       Date:  2011-07-27       Impact factor: 5.269

5.  MRI assessment of cerebral blood flow after experimental traumatic brain injury combined with hemorrhagic shock in mice.

Authors:  Lesley M Foley; Alia M Iqbal O'Meara; Stephen R Wisniewski; T Kevin Hitchens; John A Melick; Chien Ho; Larry W Jenkins; Patrick M Kochanek
Journal:  J Cereb Blood Flow Metab       Date:  2012-10-17       Impact factor: 6.200

6.  Resuscitation of traumatic brain injury and hemorrhagic shock with polynitroxylated albumin, hextend, hypertonic saline, and lactated Ringer's: Effects on acute hemodynamics, survival, and neuronal death in mice.

Authors:  Jennifer L Exo; David K Shellington; Hülya Bayir; Vincent A Vagni; Keri Janesco-Feldman; Lil Ma; Carleton J Hsia; Robert S B Clark; Larry W Jenkins; C Edward Dixon; Patrick M Kochanek
Journal:  J Neurotrauma       Date:  2009-12       Impact factor: 5.269

7.  The effects of age and ketogenic diet on local cerebral metabolic rates of glucose after controlled cortical impact injury in rats.

Authors:  Mayumi L Prins; David A Hovda
Journal:  J Neurotrauma       Date:  2009-07       Impact factor: 5.269

Review 8.  Traumatic brain injury using mouse models.

Authors:  Yi Ping Zhang; Jun Cai; Lisa B E Shields; Naikui Liu; Xiao-Ming Xu; Christopher B Shields
Journal:  Transl Stroke Res       Date:  2014-02-05       Impact factor: 6.829

9.  Duration of ATP reduction affects extent of CA1 cell death in rat models of fluid percussion injury combined with secondary ischemia.

Authors:  Naoki Aoyama; Stefan M Lee; Nobuhiro Moro; David A Hovda; Richard L Sutton
Journal:  Brain Res       Date:  2008-07-09       Impact factor: 3.252

10.  Temporal profile of cerebrospinal fluid, plasma, and brain interleukin-6 after normothermic fluid-percussion brain injury: effect of secondary hypoxia.

Authors:  Katina Chatzipanteli; Elizabeth Vitarbo; Ofelia F Alonso; Helen M Bramlett; W Dalton Dietrich
Journal:  Ther Hypothermia Temp Manag       Date:  2012-12       Impact factor: 1.286

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