Lu W, Wolf M E
Department of Neuroscience, Finch University of Health Sciences/The Chicago Medical School, North Chicago, Illinois 60064, USA.
Synapse. 1999 May;32(2):119-31. doi: 10.1002/(SICI)1098-2396(199905)32:2<119::AID-SYN5>3.0.CO;2-F.
Glutamate is critical for the induction and maintenance of behavioral sensitization and associated neuroadaptations in the mesocorticolimbic dopamine (DA) system. We have shown previously [Lu et al. (1997) Synapse 26:269-280] that repeated amphetamine administration alters AMPA receptor subunit mRNA levels in rat nucleus accumbens (NAc) and medial prefrontal cortex (PFC). The present study determined if amphetamine elicits corresponding changes in AMPA receptor subunit immunolabeling. Rats were injected with amphetamine sulphate (5 mg/kg/day) or saline for 5 days and perfused 3 or 14 days after the last injection. AMPA receptor subunit immunolabeling was quantified using autoradiographic immunocytochemistry. In the NAc, GluR1 and GluR2 immunolabeling were unchanged after 3 days of withdrawal, but both were decreased significantly after 14 days of withdrawal (GluR1, 85.5+/-2.6% of control group, P<0.01; GluR2, 79.2+/-3.2%, P<0.01). Analysis of core and shell subregions at the 14-day withdrawal time indicated that GluR1 immunolabeling decreased significantly in shell, while GluR2 immunolabeling decreased significantly in both core and shell. No changes in GluR2/3, GluR2/4, or GluR4 immunolabeling in NAc were found at either withdrawal time. In the PFC, GluR1 immunolabeling increased after 3 days of withdrawal (115.3+/-7.0%, P<0.01) but returned to control levels after 14 days. The present results correspond well with our previous findings at the mRNA level. These alterations in AMPA receptor expression may account for previously described changes in the electrophysiological responsiveness of NAc and PFC neurons to glutamate and AMPA. Along with alterations in DA function, they may contribute to drug-induced dysregulation of reward-related neurotransmission.
谷氨酸对于中脑边缘多巴胺(DA)系统中行为敏化及相关神经适应性的诱导和维持至关重要。我们之前已经表明[Lu等人(1997年),《突触》26:269 - 280],反复给予苯丙胺会改变大鼠伏隔核(NAc)和内侧前额叶皮质(PFC)中AMPA受体亚基的mRNA水平。本研究确定苯丙胺是否会引起AMPA受体亚基免疫标记的相应变化。给大鼠注射硫酸苯丙胺(5毫克/千克/天)或生理盐水,持续5天,并在最后一次注射后3天或14天进行灌注。使用放射自显影免疫细胞化学对AMPA受体亚基免疫标记进行定量分析。在NAc中,戒断3天后,GluR1和GluR2免疫标记没有变化,但戒断14天后两者均显著降低(GluR1,对照组的85.5±2.6%,P<0.01;GluR2,79.2±3.2%,P<0.01)。在戒断14天时对核心和壳亚区域的分析表明,壳区域的GluR1免疫标记显著降低,而核心和壳区域的GluR2免疫标记均显著降低。在两个戒断时间点,NAc中GluR2/3、GluR2/4或GluR4免疫标记均未发现变化。在PFC中,戒断3天后GluR1免疫标记增加(115.3±7.0%,P<0.01),但14天后恢复到对照水平。目前的结果与我们之前在mRNA水平上的发现非常吻合。AMPA受体表达的这些改变可能解释了先前描述的NAc和PFC神经元对谷氨酸和AMPA的电生理反应性变化。连同DA功能的改变,它们可能导致药物诱导的与奖赏相关的神经传递失调。