A model of traumatic brain injury in rats is influenced by neuroprotection of diurnal variation which improves motor behavior and histopathology in white matter myelin

被引:2
作者
Martinez-Tapia, R. J. [1 ]
Estrada-Rojo, F. [1 ]
Lopez-Aceves, T. G. [1 ,2 ]
Garcia-Velasco, S. [1 ]
Rodriguez-Mata, V. [3 ]
Pulido-Camarillo, E. [3 ]
Perez-Torres, A. [3 ]
Lopez-Flores, E. Y. [4 ]
Ugalde-Muniz, P. [1 ]
Noriega-Navarro, R. [1 ]
Navarro, L. [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Med, Dept Fisiol, Lab Neuroendocrinol, Mexico City, DF, Mexico
[2] Univ Autonoma Sinaloa, Fac Ciencias Quim Biol, Programa Reg Posgrad Biotecnol, Culiacan, Sinaloa, Mexico
[3] Univ Nacl Autonoma Mexico, Fac Med, Dept Biol Celular & Tisular, Mexico City, DF, Mexico
[4] ISSSTE, Anat Patol, CMN Noviembre 20, Mexico City, DF, Mexico
关键词
Traumatic brain injury; Diurnal variation; White matter; Myelin; Neuroprotection; CORPUS-CALLOSUM; DAMAGE; DEFICITS; CORTEX; NMDA;
D O I
10.1016/j.heliyon.2023.e16088
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Traumatic brain injury (TBI) represents a significant public health concern and has been asso-ciated with high rates of morbidity and mortality. TBI generates two types of brain damage: primary and secondary. Secondary damage originates a series of pathophysiological processes, which include metabolic crisis, excitotoxicity, and neuroinflammation, which have deleterious consequences for neuronal function. However, neuroprotective mechanisms are also activated. The balance among these tissue responses, and its variations throughout the day determines the fate of the damage tissue. We have demonstrated less behavioral and morphological damage when a rat model of TBI was induced during the light hours of the day.Moreover, here we show that rats subjected to TBI in the dark lost less body weight than those subjected to TBI in the light, despite no change in food intake. Besides, the rats subjected to TBI in the dark had better performance in the beam walking test and presented less histological damage in the corpus callosum and the cingulum bundle, as shown by the Kluver-Barrera staining.Our results suggest that the time of day when the injury occurs is important. Thus, this data should be used to evaluate the pathophysiological processes of TBI events and develop better therapies.
引用
收藏
页数:11
相关论文
共 56 条
[1]   Myelin and oligodendrocyte lineage cells in white matter pathology and plasticity after traumatic brain injury [J].
Armstrong, Regina C. ;
Mierzwa, Amanda J. ;
Sullivan, Genevieve M. ;
Sanchez, Maria A. .
NEUROPHARMACOLOGY, 2016, 110 :654-659
[2]   Anterior and middle cranial fossa in traumatic brain injury: Relevant neuroanatomy and neuropathology in the study of neuropsychological outcome [J].
Bigler, Erin D. .
NEUROPSYCHOLOGY, 2007, 21 (05) :515-531
[3]   Experimental Designs for Repeated Mild Traumatic Brain Injury: Challenges and Considerations [J].
Bolton-Hall, Amanda N. ;
Hubbard, W. Brad ;
Saatman, Kathryn E. .
JOURNAL OF NEUROTRAUMA, 2019, 36 (08) :1203-1221
[4]   Default Mode Network Connectivity Predicts Sustained Attention Deficits after Traumatic Brain Injury [J].
Bonnelle, Valerie ;
Leech, Robert ;
Kinnunen, Kirsi M. ;
Ham, Tim E. ;
Beckmann, Cristian F. ;
De Boissezon, Xavier ;
Greenwood, Richard J. ;
Sharp, David J. .
JOURNAL OF NEUROSCIENCE, 2011, 31 (38) :13442-13451
[5]   White matter damage after traumatic brain injury: A role for damage associated molecular patterns [J].
Braun, Molly ;
Vaibhav, Kumar ;
Saad, Nancy M. ;
Fatima, Sumbul ;
Vender, John R. ;
Baban, Babak ;
Hoda, Md Nasrul ;
Dhandapani, Krishnan M. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2017, 1863 (10) :2614-2626
[6]   Cerebral metabolism following traumatic brain injury: new discoveries with implications for treatment [J].
Brooks, George A. ;
Martin, Neil A. .
FRONTIERS IN NEUROSCIENCE, 2015, 8
[7]   The cingulum bundle: Anatomy, function, and dysfunction [J].
Bubb, Emma J. ;
Metzler-Baddeley, Claudia ;
Aggleton, John P. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2018, 92 :104-127
[8]  
Burke J.F., 1979, ANN SURG, P10
[9]  
Centers for Disease Control and Prevention, 2015, Report to Congress on Traumatic Brain Injury in the United States: Epidemiology and Rehabilitation
[10]   The AMPAR Antagonist Perampanel Attenuates Traumatic Brain Injury Through Anti-Oxidative and Anti-Inflammatory Activity [J].
Chen, Tao ;
Dai, Shu-Hui ;
Jiang, Zhi-Quan ;
Luo, Peng ;
Jiang, Xiao-Fan ;
Fei, Zhou ;
Gui, Song-Bai ;
Qi, Yi-Long .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2017, 37 (01) :43-52