Alterations in AMPA receptor subunit expression after experimental spinal cord contusion injury

被引:86
作者
Grossman, SD
Wolfe, BB
Yasuda, RP
Wrathall, JR
机构
[1] Georgetown Univ, Med Ctr, Dept Cell Biol, Washington, DC 20007 USA
[2] Georgetown Univ, Med Ctr, Dept Pharmacol, Washington, DC 20007 USA
关键词
AMPA receptor; spinal cord injury; excitatory amino acids; GluR2; motor neurons; rat; Western blot; in situ hybridization; antibodies;
D O I
10.1523/JNEUROSCI.19-14-05711.1999
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The AMPA-preferring subtype of ionotropic glutamate receptors (GluRs) is a hetero-oligomeric ion channel assembled from various combinations of four subunits: GluR1, GluR2, GluR3, and GluR4. Antagonists of these receptors can mitigate the effects of experimental spinal cord injury (SCI), indicating that these receptors play a significant role in pathophysiology after spinal trauma. We tested the hypothesis that SCI alters expression of AMPA receptors using a standardized thoracic weight-drop model of rat contusive spinal cord injury. AMPA receptor subunit expression was measured at 24 hr and at 1 month after SCI with quantitative Western blot analysis and in situ hybridization. GluR2 protein levels were preferentially reduced near the injury site 24 hr after SCI. This reduction persisted at 1 month. At a cellular level, a significant decrease in both GluR2 and GluR4 mRNA was found in spared ventral motor neurons adjacent to the injury site and distal to it, with other AMPA subunit mRNAs maintained at control levels. In contrast, only GluR1 mRNA was decreased in the sympathetic preganglionic neurons of the intermediolateral horn. These results suggest population-specific and long-lasting changes in neuronal AMPA receptor composition, which may alter response to glutamate after SCI. These alterations may contribute not only to acute neuropathological consequences of injury, but they may also be partially responsible for the altered functional state of preserved tissue seen chronically after SCI.
引用
收藏
页码:5711 / 5720
页数:10
相关论文
共 77 条
[1]   Differential vulnerability of autonomic and somatic motor neurons to N-methyl-D-aspartate-induced excitotoxicity [J].
Annis, CM ;
Vaughn, JE .
NEUROSCIENCE, 1998, 83 (01) :239-249
[2]   Aurintricarboxylic acid prevents GLUR2 mRNA down-regulation and delayed neurodegeneration in hippocampal CA1 neurons of gerbil after globalischemia [J].
Aronica, EM ;
Gorter, JA ;
Grooms, S ;
Kessler, JA ;
Bennett, MVL ;
Zukin, RS ;
Rosenbaum, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :7115-7120
[3]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[4]   EVIDENCE FOR ALTERATIONS OF SYNAPTIC INPUTS TO SACRAL SPINAL REFLEX CIRCUITS AFTER SPINAL-CORD TRANSECTION IN THE CAT [J].
BEATTIE, MS ;
LEEDY, MG ;
BRESNAHAN, JC .
EXPERIMENTAL NEUROLOGY, 1993, 123 (01) :35-50
[5]   The GluR2 (GluRB) hypothesis in ischemia: missing links [J].
Ben-Ari, Y ;
Khrestchatisky, M .
TRENDS IN NEUROSCIENCES, 1998, 21 (06) :241-242
[6]  
Bennett MVL, 1996, COLD SPRING HARB SYM, V61, P373
[7]   Calcium permeability of glutamate-gated channels in the central nervous system [J].
Burnashev, N .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (03) :311-317
[8]  
Carriedo SG, 1996, J NEUROSCI, V16, P4069
[9]  
CHOI DW, 1994, PROG BRAIN RES, V100, P47
[10]   EVIDENCE FOR CALCIUM REGULATION OF SPINAL-CORD MOTONEURON DEATH IN THE CHICK-EMBRYO IN-VIVO [J].
CIUTAT, D ;
ESQUERDA, JE ;
CALDERO, J .
DEVELOPMENTAL BRAIN RESEARCH, 1995, 86 (1-2) :167-179