Angulo J A, Williams A, Ledoux M, Watanabe Y, McEwen B S
Department of Biological Sciences, Hunter College, City University of New York, NY 10021, USA.
Brain Res Mol Brain Res. 1995 Mar;29(1):15-22. doi: 10.1016/0169-328x(94)00223-2.
The effect of N-methyl-D-aspartate (NMDA) receptor blockade on the expression of preproenkephalin (PPE), preprotachykinin (PPT) and preprodynorphin (PPD) mRNAs in the caudate-putamen and nucleus accumbens was assessed with the non-competitive NMDA receptor antagonist MK-801. Administration of MK-801 once daily for 7 consecutive days increased the abundance of all three neuropeptide mRNAs in the caudate-putamen (CPU) and nucleus accumbens (NAc). (1) PPE mRNA abundance was increased in the anterior CPU (26%) as well as dorsal and ventral CPU (46% and 39%, respectively) but was unaffected in the NAc. (2) PPT mRNA was increased in the NAc (33%), anterior CPU (27%), dorsal CPU (43%) and ventral CPU (67%). In the ventral CPU, PPT mRNA abundance doubled when the dose of MK-801 increased two-fold (from 67% to 119% above control). (3) PPD mRNA was elevated in dorsal and ventral regions of the CPU (49% and 24%, respectively) and in anterior CPU (50%). In the NAc PPD mRNA was increased only at the higher dose (0.1 mg/kg) of MK-801. Cellular analysis of the distribution of grains per cell shows that increases are due to increased accumulation of mRNA by previously expressing cells of the CPU and NAc. These observations demonstrate that NMDA receptor activity plays a significant role in the regulation of neuropeptide expression in the caudate-putamen and accumbens of the rat brain.
使用非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK-801评估NMDA受体阻断对尾状核-壳核及伏隔核中前脑啡肽原(PPE)、前速激肽原(PPT)和前强啡肽原(PPD)mRNA表达的影响。连续7天每天给予MK-801可增加尾状核-壳核(CPU)和伏隔核(NAc)中所有三种神经肽mRNA的丰度。(1)PPE mRNA丰度在前部CPU中增加(26%),在背侧和腹侧CPU中也增加(分别为46%和39%),但在NAc中未受影响。(2)PPT mRNA在NAc中增加(33%),在前部CPU中增加(27%),在背侧CPU中增加(43%),在腹侧CPU中增加(67%)。在腹侧CPU中,当MK-801剂量增加两倍时(从比对照高67%增至119%),PPT mRNA丰度翻倍。(3)PPD mRNA在CPU的背侧和腹侧区域升高(分别为49%和24%),在前部CPU中升高(50%)。在NAc中,PPD mRNA仅在较高剂量(0.1 mg/kg)的MK-801作用下增加。对每个细胞中颗粒分布的细胞分析表明,增加是由于CPU和NAc中先前表达细胞的mRNA积累增加所致。这些观察结果表明,NMDA受体活性在大鼠脑尾状核-壳核及伏隔核中神经肽表达的调节中起重要作用。