Van Keuren K R, Stodgell C J, Schroeder S R, Tessel R E
Department of Pharmacology, Schiefelbusch Institute for Life Span Studies, School of Pharmacy, University of Kansas, Lawrence 66045-2505, USA.
Brain Res. 1998 Jan 5;780(1):56-66. doi: 10.1016/s0006-8993(97)01184-0.
Severe 6-hydroxydopamine (6-OHDA)-induced neostriatal dopamine (DA) depletion is generally held to be irreversible. Adult rats administered 6-OHDA soon after weaning, or neonatally, respectively model Parkinson's disease (PD) and Lesch-Nyhan syndrome (LNS). Prior studies in our laboratory indicate that prolonged training on incrementally more difficult fixed-ratio (FR) discriminations can reverse 'irreversible' 6-OHDA-induced neostriatal DA depletion in adult LNS rats. The present study evaluated the effects of such training on neostriatal DA depletion and its functional consequences in adult PD and control (vehicle-injected) rats. After recovery from 6-OHDA-induced hypophagia, rats were sacrificed to assess neostriatal DA depletion magnitude, or were food-deprived and either subjected to food-maintained operant FR discrimination training or allowed to remain in their home cages. 6-OHDA treatment antagonized amphetamine (AMP)-induced increases in brief rearing behavior and locomotor activity in 3-month-old PD rats prior to training, and reduced operant response rates throughout training without affecting learning rates. One week after training, AMP-increased locomotor and brief-rearing frequencies were augmented in all groups except trained controls, and the prior inhibitory effect of 6-OHDA treatment on AMP-increased behavioral frequencies was essentially eliminated. Cumulative apomorphine (APO) dose-effect curve (0.1-3.2 mg/kg) construction 3 weeks post-training revealed that 6-OHDA treatment abolished APO-induced intense licking behavior. However, training eliminated the hyperresponsiveness of 6-OHDA-treated rats to the locomotor- and brief-rearing stimulant effects of APO but did not affect the depletion of neostriatal DA. Nevertheless, 6-OHDA-induced increases in neostriatal DOPAC/DA and HVA/DA ratios were normalized by age/food-deprivation while that of 3MT/DA was not. These findings suggest that training reduces the functional responsiveness of at least some central DA receptors, FR discrimination training could be a useful adjunct to PD replacement therapy and that the neostriatal DA-repleting action of training in 6-OHDA-treated rats depend on the age at which 6-OHDA is administered.
严重的6-羟基多巴胺(6-OHDA)诱导的新纹状体多巴胺(DA)耗竭通常被认为是不可逆的。分别在断奶后不久或新生时给予6-OHDA的成年大鼠可模拟帕金森病(PD)和莱施-奈恩综合征(LNS)。我们实验室先前的研究表明,对难度逐渐增加的固定比率(FR)辨别任务进行长期训练,可以逆转成年LNS大鼠中“不可逆的”6-OHDA诱导的新纹状体DA耗竭。本研究评估了这种训练对成年PD大鼠和对照(注射赋形剂)大鼠新纹状体DA耗竭及其功能后果的影响。从6-OHDA诱导的摄食减少中恢复后,处死大鼠以评估新纹状体DA耗竭程度,或者使大鼠禁食,并使其接受以食物维持的操作性FR辨别训练,或者让其留在笼中。在训练前,6-OHDA处理拮抗了3月龄PD大鼠中苯丙胺(AMP)诱导的短暂竖毛行为和运动活动增加,并在整个训练过程中降低了操作性反应率,而不影响学习率。训练一周后,除训练对照外,所有组中AMP增加的运动和短暂竖毛频率均增加,并且6-OHDA处理对AMP增加的行为频率的先前抑制作用基本消除。训练3周后构建的累积阿扑吗啡(APO)剂量效应曲线(0.1 - 3.2 mg/kg)显示,6-OHDA处理消除了APO诱导的强烈舔舐行为。然而,训练消除了6-OHDA处理大鼠对APO的运动和短暂竖毛刺激作用的高反应性,但不影响新纹状体DA的耗竭。尽管如此,6-OHDA诱导的新纹状体DOPAC/DA和HVA/DA比值增加通过年龄/禁食得以正常化,而3MT/DA比值则未正常化。这些发现表明,训练降低了至少一些中枢DA受体的功能反应性,FR辨别训练可能是PD替代疗法的有用辅助手段,并且在6-OHDA处理的大鼠中训练的新纹状体DA补充作用取决于给予6-OHDA的年龄。