Nowak Przemyslaw, Bortel Aleksandra, Dabrowska Joanna, Oswiecimska Joanna, Drosik Marzena, Kwiecinski Adam, Opara Józef, Kostrzewa Richard M, Brus Ryszard
Department of Pharmacology, Medical University of Silesia, H. Jordana 38, 41-808 Zabrze, Poland.
Neurotox Res. 2007 Feb;11(2):131-44. doi: 10.1007/BF03033391.
In the neonatally 6-hydroxydopamine (6-OHDA)-lesioned rat hyperlocomotor activity, first described in the 1970s, was subsequently found to be increased by an additional lesion with 5,7-dihydroxytryptamine (5,7-DHT) (i.c.v.) in adulthood. The latter animal model (i.e., 134 microg 6-OHDA at 3 d postbirth plus 71 microg 5,7-DHT at 10 weeks; desipramine pretreatments) was used in this study, in an attempt to attribute hyperlocomotor attenuation by D,L-amphetamine sulfate (AMPH) and m-chlorophenylpiperazine di HCl (mCPP), to specific changes in extraneuronal (i.e., in vivo microdialysate) levels of dopamine (DA) and/or serotonin (5-HT). Despite the 98-99% reduction in striatal tissue content of DA, the baseline striatal microdialysate level of DA was reduced by 50% or less at 14 weeks, versus the intact control group. When challenged with AMPH (0.5 mg/kg), the microdialysate level of DA went either unchanged or was slightly reduced over the next 180 min (i.e., 20 min sampling), while in the vehicle group and 5,7-DHT (alone) lesioned group, the microdialysate level was maximally elevated by approximately 225% and approximately 450%, respectively--and over a span of nearly 2 h. Acute challenge with mCPP (1 mg/kg salt form) had little effect on microdialysate levels of DA, DOPAC and 5-HT. Moreover, there was no consistent change in the microdialysate levels of DA, DOPAC, and 5-HT between intact, 5-HT-lesioned rats, and DA-lesioned rats which might reasonably account for an attenuation of hyperlocomotor activity. These findings indicate that there are other important neurochemical changes produced by AMPH- and mCPP-attenuated hyperlocomotor activity, or perhaps a different brain region or multiple brain regional effects are involved in AMPH and mCPP behavioral actions.
20世纪70年代首次描述了新生大鼠经6-羟基多巴胺(6-OHDA)损伤后出现运动亢进活动,随后发现成年期再次经5,7-二羟基色胺(5,7-DHT)(脑室内注射)损伤会加剧这种活动。本研究采用了后一种动物模型(即出生后3天注射134微克6-OHDA,10周时注射71微克5,7-DHT;预先给予地昔帕明治疗),试图将硫酸D,L-苯丙胺(AMPH)和盐酸间氯苯哌嗪(mCPP)导致的运动亢进减弱归因于细胞外(即体内微透析液)多巴胺(DA)和/或5-羟色胺(5-HT)水平的特定变化。尽管纹状体组织中DA含量减少了98%-99%,但与完整对照组相比,14周时纹状体微透析液中DA的基线水平降低了50%或更低。当用AMPH(0.5毫克/千克)进行刺激时,在接下来的180分钟(即20分钟取样一次)内,微透析液中DA的水平要么没有变化,要么略有降低,而在溶剂对照组和5,7-DHT(单独)损伤组中,微透析液中DA的水平分别在近2小时内最大升高了约225%和约450%。用mCPP(1毫克/千克盐形式)进行急性刺激对微透析液中DA、3,4-二羟基苯乙酸(DOPAC)和5-HT的水平影响很小。此外,在完整大鼠、5-HT损伤大鼠和DA损伤大鼠之间,微透析液中DA、DOPAC和5-HT的水平没有一致的变化,这些变化可能合理地解释运动亢进活动的减弱。这些发现表明,AMPH和mCPP导致的运动亢进减弱还产生了其他重要的神经化学变化,或者可能涉及不同的脑区或多个脑区的作用,参与了AMPH和mCPP的行为效应。