Cortical edema in moderate fluid percussion brain injury is attenuated by vagus nerve stimulation

被引:64
作者
Clough, R. W. [1 ]
Neese, S. L.
Sherill, L. K.
Tan, A. A.
Duke, A.
Roosevelt, R. W.
Browning, R. A.
Smith, D. C.
机构
[1] So Illinois Univ, Sch Med, Dept Anat, Carbondale, IL 62901 USA
[2] So Illinois Univ, Brain & Cognit Sci Program, Dept Psychol, Carbondale, IL 62901 USA
[3] So Illinois Univ, Dept Physiol, Sch Med, Carbondale, IL 62901 USA
[4] So Illinois Univ, Ctr Integrat Res Cognit & Neural ci, Carbondale, IL 62901 USA
关键词
traumatic brain injury; TBI; FPI; VNS; brain swelling; rats;
D O I
10.1016/j.neuroscience.2007.04.043
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Development of cerebral edema (intracellular and/or extracellular water accumulation) following traumatic brain injury contributes to mortality and morbidity that accompanies brain injury. Chronic intermittent vagus nerve stimulation (VNS) initiated at either 2 h or 24 h (VNS: 30 s train of 0.5 mA, 20 Hz, biphasic pulses every 30 min) following traumatic brain injury enhances recovery of motor and cognitive function in rats in the weeks following brain injury; however, the mechanisms of facilitated recovery are unknown. The present study examines the effects of VNS on development of acute cerebral edema following unilateral fluid percussion brain injury (FPI) in rats, concomitant with assessment of their behavioral recovery. Two hours following FPI, VNS was initiated. Behavioral testing, using both beam walk and locomotor placing tasks, was conducted at 1 and 2 days following FPI. Edema was measured 48 h post-FPI by the customary method of region-specific brain weights before and after complete dehydration. Results of this study replicated that VNS initiated at 2 h after FPI: 1) effectively facilitated the recovery of vestibulomotor function at 2 days after FPI assessed by beam walk performance (P<0.01); and 2) tended to improve locomotor placing performance at the same time point (P=0.18). Most interestingly, results of this study showed that development of edema within the cerebral cortex ipsilateral to FPI was significantly attenuated at 48 h in FPI rats receiving VNS compared with non-VNS FPI rats (P<0.04). Finally, a correlation analysis between beam walk performance and cerebral edema following FPI revealed a significant inverse correlation between behavior performance and cerebral edema. Together, these results suggest that VNS facilitation of motor recovery following experimental brain injury in rats is associated with VNS-mediated attenuation of cerebral edema. (c) 2007 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:286 / 293
页数:8
相关论文
共 64 条
[1]
FUNCTIONAL SUBDIVISIONS OF THE RAT SOMATIC SENSORIMOTOR CORTEX [J].
BARTH, TM ;
JONES, TA ;
SCHALLERT, T .
BEHAVIOURAL BRAIN RESEARCH, 1990, 39 (01) :73-95
[2]
Evidence supporting a role for N-acetyl-L-aspartate as a molecular water pump in myelinated neurons in the central nervous system -: An analytical review [J].
Baslow, MH .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (04) :295-300
[3]
Extracellular N-acetylaspartate depletion in traumatic brain injury [J].
Belli, A ;
Sen, J ;
Petzold, A ;
Russo, S ;
Kitchen, N ;
Smith, M ;
Tavazzi, B ;
Vagnozzi, R ;
Signoretti, S ;
Amorini, AM ;
Bellia, F ;
Lazzarino, G .
JOURNAL OF NEUROCHEMISTRY, 2006, 96 (03) :861-869
[4]
Dynamics of experimental vasogenic brain oedema in the rat: changes induced by adrenergic drugs [J].
Borges, N ;
Sarmento, A ;
Azevedo, I .
JOURNAL OF AUTONOMIC PHARMACOLOGY, 1999, 19 (04) :209-217
[5]
INTRAVENTRICULAR NOREPINEPHRINE FACILITATES MOTOR RECOVERY FOLLOWING SENSORIMOTOR CORTEX INJURY [J].
BOYESON, MG ;
FEENEY, DM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 35 (03) :497-501
[6]
BOYESON MG, 1993, RESTOR NEUROL NEUROS, V5, P283, DOI 10.3233/RNN-1993-5404
[7]
BIOCHEMICAL AND BEHAVIORAL-EFFECTS OF A SENSORIMOTOR CORTEX INJURY IN RATS PRETREATED WITH THE NORADRENERGIC NEUROTOXIN DSP-4 [J].
BOYESON, MG ;
CALLISTER, TR ;
CAVAZOS, JE .
BEHAVIORAL NEUROSCIENCE, 1992, 106 (06) :964-973
[8]
Exacerbation of cortical and hippocampal CA1 damage due to posttraumatic hypoxia following moderate fluid-percussion brain injury in rats [J].
Bramlett, HM ;
Green, EJ ;
Dietrich, WD .
JOURNAL OF NEUROSURGERY, 1999, 91 (04) :653-659
[9]
The maxi-K channel opener EMS-204352 attenuates regional cerebral edema and neurologic motor impairment after experimental brain injury [J].
Cheney, JA ;
Weisser, JD ;
Bareyre, FM ;
Laurer, HL ;
Saatman, KE ;
Raghupathi, R ;
Gribkoff, V ;
Starrett, JE ;
McIntosh, TK .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (04) :396-403
[10]
CLOUGH RW, 2006, J NEUROTRAUM, V22, P1258