Narita Minoru, Takagi Misa, Aoki Kazue, Kuzumaki Naoko, Suzuki Tsutomu
Department of Toxicology, School of Pharmacy and Pharmaceutical Science, Hoshi University, Shinagawa-ku, Tokyo, Japan.
J Neurochem. 2003 Jul;86(2):273-82. doi: 10.1046/j.1471-4159.2003.01784.x.
A growing body of evidence suggests that several protein kinases are involved in the expression of pharmacological actions induced by a psychostimulant methamphetamine. The present study was designed to investigate the role of the Rho/Rho-associated kinase (ROCK)-dependent pathway in the expression of the increase in extracellular levels of dopamine in the nucleus accumbens and its related behaviors induced by methamphetamine in rats. Methamphetamine (1 mg/kg, subcutaneously) produced a substantial increase in extracellular levels of dopamine in the nucleus accumbens, with a progressive augmentation of dopamine-related behaviors including rearing and sniffing. Methamphetamine also induced the decrease in levels of its major metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanilic acid (HVA). Both the increase in extracellular levels of dopamine and the induction of dopamine-related behaviors by methamphetamine were significantly suppressed by pretreatment with an intranucleus accumbens injection of a selective ROCK inhibitor Y-27632. In contrast, Y-27632 had no effect on the decrease in levels of DOPAC and HVA induced by methamphetamine. Under these conditions, there were no changes in protein levels of membrane-bound RhoA in the nucleus accumbens following methamphetamine treatment. It is of interest to note that the microinjection of Y-27632 into the nucleus accumbens failed to suppress the increases in extracellular levels of dopamine, DOPAC, and HVA in the nucleus accumbens induced by subcutaneous injection of a prototype of micro -opioid receptor agonist morphine (10 mg/kg). Furthermore, perfusion of a selective blocker of voltage-dependent Na+ channels, tetrodotoxin (TTx) into the rat nucleus accumbens did not affect the increase in extracellular levels of dopamine in the rat nucleus accumbens by methamphetamine, whereas the morphine-induced dopamine elevation was eliminated by this application of TTx. The extracellular level of dopamine in the nucleus accumbens was also increased by perfusion of a selective dopamine re-uptake inhibitor 1-[2-[bis(4-fluorophenyl)methoxy]-4-(3-phenylpropyl)piperazine (GBR-12909) in the nucleus accumbens. This effect was not affected by pretreatment with intranucleus accumbens injection of Y-27632. These findings provide first evidence that Rho/ROCK pathway in the nucleus accumbens may contribute to the increase in extracellular levels of dopamine in the nucleus accumbens evoked by a single subcutaneous injection of methamphetamine. In contrast, this pathway is not essential for the increased level of dopamine in this region induced by morphine, providing further evidence for the different mechanisms of dopamine release by methamphetamine and morphine in rats.
越来越多的证据表明,几种蛋白激酶参与了精神兴奋剂甲基苯丙胺诱导的药理作用的表达。本研究旨在探讨Rho/ Rho相关激酶(ROCK)依赖性通路在甲基苯丙胺诱导的大鼠伏隔核细胞外多巴胺水平升高及其相关行为表达中的作用。甲基苯丙胺(1mg/kg,皮下注射)使伏隔核细胞外多巴胺水平显著升高,同时与多巴胺相关的行为(如竖毛和嗅探)逐渐增强。甲基苯丙胺还导致其主要代谢产物3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA)水平降低。伏隔核内注射选择性ROCK抑制剂Y-27632预处理可显著抑制甲基苯丙胺诱导的细胞外多巴胺水平升高以及多巴胺相关行为。相反,Y-27632对甲基苯丙胺诱导的DOPAC和HVA水平降低没有影响。在这些条件下,甲基苯丙胺处理后伏隔核中膜结合RhoA的蛋白水平没有变化。值得注意的是,向伏隔核内微量注射Y-27632未能抑制皮下注射微阿片受体激动剂吗啡(10mg/kg)诱导的伏隔核细胞外多巴胺、DOPAC和HVA水平升高。此外,向大鼠伏隔核灌注电压依赖性Na+通道的选择性阻滞剂河豚毒素(TTX)并不影响甲基苯丙胺诱导的大鼠伏隔核细胞外多巴胺水平升高,而这种TTX的应用消除了吗啡诱导的多巴胺升高。向伏隔核灌注选择性多巴胺再摄取抑制剂1-[2-[双(4-氟苯基)甲氧基]-4-(3-苯丙基)哌嗪(GBR-12909)也可使伏隔核中的多巴胺细胞外水平升高。伏隔核内注射Y-27632预处理对这种作用没有影响。这些发现首次证明,伏隔核中的Rho/ROCK通路可能有助于单次皮下注射甲基苯丙胺引起的伏隔核细胞外多巴胺水平升高。相反,该通路对于吗啡诱导的该区域多巴胺水平升高并非必不可少,这为甲基苯丙胺和吗啡在大鼠体内释放多巴胺的不同机制提供了进一步的证据。