Standaert D G, Testa C M, Rudolf G D, Hollingsworth Z R
Department of Neurology, Massachusetts General Hospital, Boston, USA.
J Pharmacol Exp Ther. 1996 Jan;276(1):342-52.
N-methyl-D-aspartate (NMDA) glutamate receptors have an established role in the regulation of motor behavior by the basal ganglia. Recent studies have revealed that NMDA receptors are heteromeric assemblies of structurally related subunits from two families: NMDAR1, which is required for channel activity, and NMDAR2A-D, which modulate the properties of the channels. In the rat, the NMDA receptor subunits exhibit anatomically restricted patterns of expression, so that each component of the basal ganglia has a distinct NMDA receptor subunit mRNA phenotype. We have used in vivo intrastriatal injection of synthetic antisense oligodeoxynucleotides (ODNs) to examine the roles of particular NMDA receptor subunits in the regulation of motor behavior in rats. Injection of 15 nmol of a 20-mer ODN targeted to the NMDAR1 subunit induced spontaneous ipsilateral rotation. Smaller doses of NMDAR1 antisense ODN did not lead to spontaneous rotation, but prominent ipsilateral rotation was observed after systemic administration of D-amphetamine. An antisense ODN to NMDAR2A was also effective in eliciting amphetamine-inducible rotation, although the magnitude of the effect was less than that seen with NMDAR1, whereas ODNs targeted to NMDAR2B, NMDAR2C and an NMDAR1 sense strand ODN had no effect on behavior. In situ hybridization demonstrated that injection of the NMDAR1, NMDAR2A or NMDAR2B antisense ODNs produced specific reductions in target mRNA signal intensity in the injected striatum. After NMDAR1 antisense ODN injection, striatal binding of 3H-glutamate target mRNA signal intensity in the injected striatum. After NMDAR1 antisense ODN injection, striatal binding of 3H-glutamate to NMDA sites was not altered, although strychnine-insensitive 3H-glycine binding sites exhibited a small but significant reduction. These observations suggest that NMDA receptor complexes containing NMDAR1 and, to a lesser extent, NMDAR2A subunits play particularly important roles in the regulation of motor behavior by neostriatal neurons.
N-甲基-D-天冬氨酸(NMDA)谷氨酸受体在基底神经节对运动行为的调节中具有既定作用。最近的研究表明,NMDA受体是来自两个家族的结构相关亚基的异源寡聚体:通道活性所必需的NMDAR1,以及调节通道特性的NMDAR2A-D。在大鼠中,NMDA受体亚基表现出解剖学上受限的表达模式,因此基底神经节的每个组成部分都有独特的NMDA受体亚基mRNA表型。我们通过在体纹状体内注射合成反义寡脱氧核苷酸(ODN)来研究特定NMDA受体亚基在大鼠运动行为调节中的作用。注射15 nmol靶向NMDAR1亚基的20聚体ODN会诱导自发的同侧旋转。较小剂量的NMDAR1反义ODN不会导致自发旋转,但在全身给予D-苯丙胺后观察到明显的同侧旋转。针对NMDAR2A的反义ODN在引发苯丙胺诱导的旋转方面也有效,尽管效果的程度小于NMDAR1,而靶向NMDAR2B、NMDAR2C的ODN和NMDAR1正义链ODN对行为没有影响。原位杂交表明,注射NMDAR1、NMDAR2A或NMDAR2B反义ODN会使注射纹状体内的靶mRNA信号强度特异性降低。注射NMDAR