Literature DB >> 3225860

Physiologic, histopathologic, and cineradiographic characterization of a new fluid-percussion model of experimental brain injury in the rat.

C E Dixon1, J W Lighthall, T E Anderson.   

Abstract

The fluid-percussion technique produces experimental brain injury by rapid injection of a fluid volume into the closed cranial cavity. The experiments reported here characterize a new, more controlled technique for fluid-percussion brain injury in the rat and systematically examine systemic physiologic, histopathologic, and electroencephalographic responses in the rat at two levels of injury severity. The new technique was developed to permit independent variation of the fluid pressure pulse parameters and, thus, more accurately define the brain loading conditions associated with fluid-percussion injury. The new technique produced changes in mean arterial blood pressure similar to previous techniques; however, bradycardia was not observed. Significant increases in heart rate were produced by both injury levels and were more prolonged at the high level of injury severity. Both magnitudes of injury produced significant decreases in EEG amplitude immediately postinjury, but high severity injury produced a greater decrease in delta frequency band (1-4 Hz) activity than did low severity injury. Both levels produced hemorrhage at the site of injury, thalamus, corpus callosum, hippocampus, and fimbria hippocampus similar to previous techniques. Higher levels of injury produced more extensive cerebral hemorrhage and greater spinal involvement. In a separate group of animals, cineradiographic images were made at coronal, sagittal, and dorsal orientations during the fluid pressure pulse. Intracranial fluid movement was characterized by rapid radial movement within the epidural space. The data suggest that the distributed nature of fluid-percussion induces pathology, and dysfunction may reflect a diffuse mechanical loading of the brain surface. The model appears to give repeatable effects useful in the study of closed head injury.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3225860     DOI: 10.1089/neu.1988.5.91

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


  27 in total

1.  CR8, a novel inhibitor of CDK, limits microglial activation, astrocytosis, neuronal loss, and neurologic dysfunction after experimental traumatic brain injury.

Authors:  Shruti V Kabadi; Bogdan A Stoica; David J Loane; Tao Luo; Alan I Faden
Journal:  J Cereb Blood Flow Metab       Date:  2014-01-08       Impact factor: 6.200

2.  Early microstructural and metabolic changes following controlled cortical impact injury in rat: a magnetic resonance imaging and spectroscopy study.

Authors:  Su Xu; Jiachen Zhuo; Jennifer Racz; Da Shi; Steven Roys; Gary Fiskum; Rao Gullapalli
Journal:  J Neurotrauma       Date:  2011-09-29       Impact factor: 5.269

3.  Increased Network Excitability Due to Altered Synaptic Inputs to Neocortical Layer V Intact and Axotomized Pyramidal Neurons after Mild Traumatic Brain Injury.

Authors:  Anders Hånell; John E Greer; Kimberle M Jacobs
Journal:  J Neurotrauma       Date:  2015-06-26       Impact factor: 5.269

4.  Animal Models of Posttraumatic Seizures and Epilepsy.

Authors:  Alexander V Glushakov; Olena Y Glushakova; Sylvain Doré; Paul R Carney; Ronald L Hayes
Journal:  Methods Mol Biol       Date:  2016

5.  Traumatic brain injury in adult rats causes progressive nigrostriatal dopaminergic cell loss and enhanced vulnerability to the pesticide paraquat.

Authors:  Che Brown Hutson; Carlos R Lazo; Farzad Mortazavi; Christopher C Giza; David Hovda; Marie-Francoise Chesselet
Journal:  J Neurotrauma       Date:  2011-09       Impact factor: 5.269

6.  EEG slow waves in traumatic brain injury: Convergent findings in mouse and man.

Authors:  Mo Modarres; Nicholas N Kuzma; Tracy Kretzmer; Allan I Pack; Miranda M Lim
Journal:  Neurobiol Sleep Circadian Rhythms       Date:  2016-07-01

7.  Diffuse traumatic axonal injury in the mouse induces atrophy, c-Jun activation, and axonal outgrowth in the axotomized neuronal population.

Authors:  John E Greer; Melissa J McGinn; John T Povlishock
Journal:  J Neurosci       Date:  2011-03-30       Impact factor: 6.167

Review 8.  Animal models of traumatic brain injury.

Authors:  Ye Xiong; Asim Mahmood; Michael Chopp
Journal:  Nat Rev Neurosci       Date:  2013-02       Impact factor: 34.870

9.  Incretin mimetics as pharmacologic tools to elucidate and as a new drug strategy to treat traumatic brain injury.

Authors:  Nigel H Greig; David Tweedie; Lital Rachmany; Yazhou Li; Vardit Rubovitch; Shaul Schreiber; Yung-Hsiao Chiang; Barry J Hoffer; Jonathan Miller; Debomoy K Lahiri; Kumar Sambamurti; Robert E Becker; Chaim G Pick
Journal:  Alzheimers Dement       Date:  2014-02       Impact factor: 21.566

10.  Deferoxamine attenuates acute hydrocephalus after traumatic brain injury in rats.

Authors:  Jinbing Zhao; Zhi Chen; Guohua Xi; Richard F Keep; Ya Hua
Journal:  Transl Stroke Res       Date:  2014-06-17       Impact factor: 6.829

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.