Adams D H, Hanson G R, Keefe K A
Department of Pharmacology and Toxicology, University of Utah, 30 South 2000 East, Rm. 201, Salt Lake City, UT 84112, USA.
Neuroscience. 2001;102(4):843-51. doi: 10.1016/s0306-4522(00)00530-3.
This study employed in situ hybridization to directly compare the effects of cocaine and methamphetamine on neurotensin/neuromedin N and preprotachykinin messenger RNAs in distinct striatal regions. Male, Sprague-Dawley rats received a single administration of 15mg/kg methamphetamine (s.c.) or 30mg/kg cocaine (i.p.) and were killed 30min or 3h later. Methamphetamine and cocaine produced significant increases in preprotachykinin messenger RNA in the striatum after 3h, but often in different subregions. Both drugs produced similar effects on preprotachykinin messenger RNA in the rostral striatum. However, methamphetamine produced significant increases in all regions of the caudal striatum, whereas cocaine-induced preprotachykinin messenger RNA expression was limited to dorsal regions of this striatal area. Methamphetamine also produced a significant increase in preprotachykinin messenger RNA in the caudal striatum after 30min, whereas cocaine had no significant effect on preprotachykinin messenger RNA at this early time-point. The pattern of changes in neurotensin/neuromedin N messenger RNA caused by methamphetamine and cocaine after 3h was even more distinct. Cocaine produced significant increases in neurotensin/neuromedin N messenger RNA in all regions of the rostral striatum, whereas methamphetamine had no effect in these areas. Furthermore, in more caudal sections, cocaine predominantly affected neurotensin/neuromedin N expression in dorsal aspects of the striatum, whereas methamphetamine significantly increased neurotensin/neuromedin N messenger RNA in all regions. There was much less effect of either drug on neuropeptide expression in the nucleus accumbens. The only significant effect was an increase in neurotensin/neuromedin N messenger RNA in the core region 3h after methamphetamine administration. These results indicate that methamphetamine and cocaine increase preprotachykinin and neurotensin/neuromedin N messenger RNAs in distinct regions of the striatum. The ability of methamphetamine and cocaine to alter neuropeptide messenger RNA expression in unique regions of the striatum may be important for the long-term effects of these drugs, such as sensitization, since the striatum is not homogeneous in its connections and function.
本研究采用原位杂交技术,直接比较可卡因和甲基苯丙胺对不同纹状体区域中神经降压素/神经介素N和前速激肽原信使核糖核酸的影响。雄性Sprague-Dawley大鼠单次皮下注射15mg/kg甲基苯丙胺或腹腔注射30mg/kg可卡因,并于30分钟或3小时后处死。3小时后,甲基苯丙胺和可卡因均使纹状体中的前速激肽原信使核糖核酸显著增加,但通常在不同的亚区域。两种药物对吻侧纹状体中的前速激肽原信使核糖核酸产生相似的影响。然而,甲基苯丙胺使尾侧纹状体的所有区域均显著增加,而可卡因诱导的前速激肽原信使核糖核酸表达仅限于该纹状体区域的背侧。30分钟后,甲基苯丙胺也使尾侧纹状体中的前速激肽原信使核糖核酸显著增加,而在此早期时间点,可卡因对前速激肽原信使核糖核酸无显著影响。3小时后,甲基苯丙胺和可卡因引起的神经降压素/神经介素N信使核糖核酸的变化模式更为明显。可卡因使吻侧纹状体的所有区域中的神经降压素/神经介素N信使核糖核酸显著增加,而甲基苯丙胺在这些区域无影响。此外,在更靠尾侧的切片中,可卡因主要影响纹状体背侧的神经降压素/神经介素N表达,而甲基苯丙胺使所有区域的神经降压素/神经介素N信使核糖核酸显著增加。两种药物对伏隔核中神经肽表达的影响要小得多。唯一显著的影响是甲基苯丙胺给药3小时后,核心区域的神经降压素/神经介素N信使核糖核酸增加。这些结果表明,甲基苯丙胺和可卡因可增加纹状体不同区域中的前速激肽原和神经降压素/神经介素N信使核糖核酸。甲基苯丙胺和可卡因在纹状体独特区域改变神经肽信使核糖核酸表达的能力,对于这些药物的长期影响(如敏化)可能很重要,因为纹状体在其连接和功能上并非均匀一致。