Anti-edema effects of rhEpo in experimental traumatic brain injury

被引:22
作者
Gatto, Rodolfo [1 ]
Chauhan, Mihir [2 ]
Chauhan, Neelima [3 ,4 ]
机构
[1] Univ Illinois, Dept Anat & Cell Biol, Chicago, IL USA
[2] Med Univ Lublin, Lublin, Poland
[3] Jesse Brown VA Med Ctr, R&D, Neurosci Res, Chicago, IL 60612 USA
[4] Univ Illinois, Dept Pediat, Chicago, IL USA
关键词
Traumatic brain injury; controlled cortical impact injury; recombinant human erythropoietin; magnetic resonance imaging; edema; AQP4; RECOMBINANT-HUMAN-ERYTHROPOIETIN; NRF2 SIGNALING PATHWAY; AGED GARLIC EXTRACT; SPINAL-CORD-INJURY; AQP4; EXPRESSION; RAT MODEL; AQUAPORIN-4; CULTURED ASTROCYTES; CEREBRAL PROTECTION; RECEPTOR ANTAGONIST;
D O I
10.3233/RNN-150577
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Purpose: Traumatic brain injury (TBI) is one of the leading causes of disability and death which begins with the formation of edema as the persistent primary causative factor in TBI. Although medical management of cerebral edema by hypothermia, ventriculostomy, mannitol or hypertonic saline have been effective in treating edema, many of these therapies end up with some neurologic deficits, necessitating novel treatment options for treating post-TBI edema. This study investigated edema reducing effects of recombinant human Erythropoietin (rhEPO) in reducing acute brain edema in the CCI mouse model of TBI. Methods: Anti-edema effects of rhEpo in reducing acute brain edema after injury in the CCI mouse model of TBI were assessed by T2 weighted magnetic resonance imaging (T2wMRI) as the accurate detector of brain edema in correlation with Western blot analysis of cerebral aquaporin 4 (AQP4) index as the critical marker of edema. Results: Results show that rhEpo treatment significantly reduced brain edema with concomitant reduction in AQP4 immuno-expression in the CCI mouse model of TBI. Conclusion: Current results emphasize clinical utility of rhEpo in treating post-TBI edema.
引用
收藏
页码:927 / 941
页数:15
相关论文
共 76 条
[1]   Induction of oxidative and nitrosative damage leads to cerebrovascular inflammation in an animal model of mild traumatic brain injury induced by primary blast [J].
Abdul-Muneer, P. M. ;
Schuetz, Heather ;
Wang, Fang ;
Skotak, Maciej ;
Jones, Joselyn ;
Gorantla, Santhi ;
Zimmerman, Matthew C. ;
Chandra, Namas ;
Haorah, James .
FREE RADICAL BIOLOGY AND MEDICINE, 2013, 60 :282-291
[2]   Clinical characteristics and pathophysiological mechanisms of focal and diffuse traumatic brain injury [J].
Andriessen, Teuntje M. J. C. ;
Jacobs, Bram ;
Vos, Pieter E. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2010, 14 (10) :2381-2392
[3]   Contribution of vasogenic and cellular edema to traumatic brain swelling measured by diffusion-weighted imaging [J].
Barzo, P ;
Marmarou, A ;
Fatouros, P ;
Hayasaki, K ;
Corwin, F .
JOURNAL OF NEUROSURGERY, 1997, 87 (06) :900-907
[4]  
Bernaudin M, 2000, GLIA, V30, P271, DOI 10.1002/(SICI)1098-1136(200005)30:3<271::AID-GLIA6>3.3.CO
[5]  
2-8
[6]   Effect of Recombinant Human Erythropoietin on Serum S100B Protein and Interleukin-6 Levels After Traumatic Brain Injury in the Rat [J].
Bian, Xiao-xing ;
Yuan, Xue-song ;
Qi, Chuan-ping .
NEUROLOGIA MEDICO-CHIRURGICA, 2010, 50 (05) :361-365
[7]   CSF-LACTATE AS A MARKER OF MITOCHONDRIAL DISORDERS EVEN IN CHILDREN AFTER BRIEF SEIZURES [J].
Magner, M. ;
Szentivanyi, K. ;
Svandova, I. ;
Jesina, P. ;
Tesarova, M. ;
Honzik, T. ;
Zeman, J. .
PEDIATRIC RESEARCH, 2010, 68 :123-123
[8]  
Byts Nadiya, 2009, Exp Transl Stroke Med, V1, P4, DOI 10.1186/2040-7378-1-4
[9]   Predicting Outcomes of Traumatic Brain Injury by Imaging Modality and Injury Distribution [J].
Chastain, Cody A. ;
Oyoyo, Udochukwu E. ;
Zipperman, Michelle ;
Joo, Elliot ;
Ashwal, Stephen ;
Shutter, Lori A. ;
Tong, Karen A. .
JOURNAL OF NEUROTRAUMA, 2009, 26 (08) :1183-1196
[10]   Propentofylline attenuates tau hyperphosphorylation in Alzheimer's Swedish mutant model Tg2576 [J].
Chauhan, NB ;
Siegel, GJ ;
Feinstein, DL .
NEUROPHARMACOLOGY, 2005, 48 (01) :93-104