Rodríguez Díaz M, Abdala P, Barroso-Chinea P, Obeso J, González-Hernández T
Department of Physiology, Faculty of Medicine, University of La Laguna, Tenerife, Canary Islands, La Laguna, Spain.
Behav Brain Res. 2001 Jul;122(1):79-92. doi: 10.1016/s0166-4328(01)00168-1.
At the beginning of the 1970s, different studies reported behavioural disturbances after the intracerebroventricular (icv) administration of 6-hydroxydopamine (6-OHDA) in the rat. Despite the fact that this neurotoxic agent degenerates brain dopaminergic (DA-) cells, its potential utility to produce a rat model of Parkinson's disease (PD) was never systematically studied because the aphagia and adipsia were often observed. In the present study, a procedure that induces a marked DA-cell degeneration that bypasses these and other undesirable complications of icv injection of 6-OHDA is reported. Lesioned animals (50-500 microg of 6-OHDA) showed a persistent motor syndrome composed of hypokinesia, purposeless chewing and catalepsy. The intensity of motor signs was dose-dependent, and recovered partially after administration of DA-receptor agonists, exposure to sensorial stimuli and stress, three procedures that reduce motor dysfunctions in Parkinson's disease (PD). Lesioned animals showed bilateral and symmetrical midbrain DA-cell degeneration with the highest cell-loss in A9 group (substantia nigra), followed by A8 (retrorubral field) and A10 (ventral tegmental area) groups. The similarity between the behavioural syndrome and the topographical profile of cell-loss after icv injection of 6-OHDA in rats and the clinical and neuropathological features of PD indicates that this may be a convenient animal model of PD particularly useful for checking in rats the possible efficacy of new anti-parkinsonian drugs on specific parameters of motor dysfunctions.
20世纪70年代初,不同的研究报道了大鼠脑室内注射6-羟基多巴胺(6-OHDA)后出现行为障碍。尽管这种神经毒性剂会使脑内多巴胺能(DA)细胞退化,但由于经常观察到摄食和饮水减少,其用于建立帕金森病(PD)大鼠模型的潜在效用从未得到系统研究。在本研究中,报告了一种诱导明显DA细胞退化的方法,该方法可避免脑室内注射6-OHDA带来的这些及其他不良并发症。造模动物(注射50-500微克6-OHDA)表现出持续的运动综合征,包括运动迟缓、无目的咀嚼和僵住症。运动症状的严重程度呈剂量依赖性,在给予DA受体激动剂、暴露于感觉刺激和应激后部分恢复,这三种方法可减轻帕金森病(PD)的运动功能障碍。造模动物表现出双侧对称的中脑DA细胞退化,A9组(黑质)细胞损失最多,其次是A8组(红核后区)和A10组(腹侧被盖区)。大鼠脑室内注射6-OHDA后的行为综合征与细胞损失的拓扑分布以及PD的临床和神经病理学特征之间的相似性表明,这可能是一种方便的PD动物模型,特别有助于在大鼠中检验新型抗帕金森病药物对运动功能障碍特定参数的可能疗效。