Voluntary exercise or amphetamine treatment, but not the combination, increases hippocampal brain-derived neurotrophic factor and synapsin I following cortical contusion injury in rats

被引:75
作者
Griesbach, G. S. [1 ]
Hovda, D. A. [1 ,2 ]
Gomez-Pinilla, F. [1 ,3 ]
Sutton, R. L. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Div Neurosurg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol Sci, Los Angeles, CA 90095 USA
关键词
controlled cortical impact; norepinephrine; oxidized proteins; running wheel; traumatic brain injury;
D O I
10.1016/j.neuroscience.2008.04.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Prior work has shown that d-amphetamine (AMPH) treatment or voluntary exercise improves cognitive functions after traumatic brain injury (TBI). In addition, voluntary exercise increases levels of brain-derived neurotrophic factor (BDNF). The current study was conducted to determine how AMPH and exercise treatments, either alone or in combination, affect molecular events that may underlie recovery following controlled cortical impact (CCI) injury in rats. We also determined if these treatments reduced injury-induced oxidative stress. Following a CCI or sham injury, rats received AMPH (1 mg/kg/day) or saline treatment via an ALZET (R) pump and were housed with or without access to a running wheel for 7 days. CCI rats ran significantly less than sham controls, but exercise level was not altered by drug treatment. On day 7 the hippocampus ipsilateral to injury was harvested and BDNF, synapsin I and phosphorylated (P) -synapsin I proteins were quantified. Exercise or AMPH alone significantly increased BDNF protein in sham and CCI rats, but this effect was lost with the combined treatment. In sham-injured rats synapsin I increased significantly after AMPH or exercise, but did not increase after combined treatment. Synapsin levels, including the P-synapsin/total synapsin ratio, were reduced from sham controls in the saline-treated CCI groups, with or without exercise. AMPH treatment significantly increased the P-synapsin/total synapsin ratio after CCI, an effect that was attenuated by combining AMPH with exercise. Exercise or AMPH treatment alone significantly decreased hippocampal carbonyl groups on oxidized proteins in the CCI rats, compared with saline-treated sedentary counterparts, but this reduction in a marker of oxidative stress was not found with the combination of exercise and AMPH treatment. These results indicate that, whereas exercise or AMPH treatment alone may induce plasticity and reduce oxidative stress after TEI, combining these treatments may cancel each other's therapeutic effects. Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:530 / 540
页数:11
相关论文
共 89 条
[1]   D-Amphetamine enhances skilled reaching after ischemic cortical lesions in rats [J].
Adkins, DL ;
Jones, TA .
NEUROSCIENCE LETTERS, 2005, 380 (03) :214-218
[2]   Brain-derived neurotrophic factor is essential for opiate-induced plasticity of noradrenergic neurons [J].
Akbarian, S ;
Rios, M ;
Liu, RJ ;
Gold, SJ ;
Fong, HF ;
Zeiler, S ;
Coppola, V ;
Tessarollo, L ;
Jones, KR ;
Nestler, EJ ;
Aghajanian, GK ;
Jaenisch, R .
JOURNAL OF NEUROSCIENCE, 2002, 22 (10) :4153-4162
[3]   The public health approach to traumatic brain injury - An overview of CDC's research and programs [J].
Binder, S ;
Corrigan, JD ;
Langlois, JA .
JOURNAL OF HEAD TRAUMA REHABILITATION, 2005, 20 (03) :189-195
[4]   INTRAVENTRICULAR NOREPINEPHRINE FACILITATES MOTOR RECOVERY FOLLOWING SENSORIMOTOR CORTEX INJURY [J].
BOYESON, MG ;
FEENEY, DM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 35 (03) :497-501
[5]   COMPARATIVE EFFECTS OF FLUOXETINE, AMITRIPTYLINE AND SEROTONIN ON FUNCTIONAL MOTOR RECOVERY AFTER SENSORIMOTOR CORTEX INJURY [J].
BOYESON, MG ;
HARMON, RL ;
JONES, JL .
AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION, 1994, 73 (02) :76-83
[6]   Modulation of use-dependent plasticity by D-amphetamine [J].
Bütefisch, CM ;
Davis, BC ;
Sawaki, L ;
Waldvogel, D ;
Classen, J ;
Kopylev, L ;
Cohen, LG .
ANNALS OF NEUROLOGY, 2002, 51 (01) :59-68
[7]   Norepinephrine induces BDNF and activates the PI-3K and MAPK cascades in embryonic hippocampal neurons [J].
Chen, M. J. ;
Nguyen, T. V. ;
Pike, C. J. ;
Russo-Neustadt, A. A. .
CELLULAR SIGNALLING, 2007, 19 (01) :114-128
[8]   Gender and environmental brain-derived neurotrophic effects on regional factor expression after experimental traumatic brain injury [J].
Chen, X ;
Li, Y ;
Kline, AE ;
Dixon, CE ;
Zafonte, RD ;
Wagner, AK .
NEUROSCIENCE, 2005, 135 (01) :11-17
[9]   Cortical edema in moderate fluid percussion brain injury is attenuated by vagus nerve stimulation [J].
Clough, R. W. ;
Neese, S. L. ;
Sherill, L. K. ;
Tan, A. A. ;
Duke, A. ;
Roosevelt, R. W. ;
Browning, R. A. ;
Smith, D. C. .
NEUROSCIENCE, 2007, 147 (02) :286-293
[10]   Delayed, selective neuronal death following experimental cortical impact injury in rats: Possible role in memory deficits [J].
Colicos, MA ;
Dixon, CE ;
Dash, PK .
BRAIN RESEARCH, 1996, 739 (1-2) :111-119