Guridi J, Herrero M T, Luquin M R, Guillén J, Ruberg M, Laguna J, Vila M, Javoy-Agid F, Agid Y, Hirsch E, Obeso J A
Department of Neurosurgery, Hospital de Navarra, Spain.
Brain. 1996 Oct;119 ( Pt 5):1717-27. doi: 10.1093/brain/119.5.1717.
Nineteen Macaca fascicularis monkeys were divided into four different groups: Group A (n = 3), control; Group B (n = 3), monkeys treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP); Group C (n = 8), animals treated with MPTP in which the subthalamic nucleus (STN) was unilaterally lesioned by kainic acid injection; in Group D (n = 5), the STN was lesioned prior to MPTP administration. Subthalamotomy resulted in a bilateral improvement of tremor, spontaneous activity, bradykinesia (evaluated by a manual motor test) and freezing in Group C. All these monkeys developed hemichorea contralateral to the lesion. The improvement was maintained and the hemichorea continued until death. The monkeys in group D showed severe hemiballism which persisted throughout MPTP administration and developed parkinsonian signs mainly on the side ipsilateral to the lesion. Analysis of the in situ hybridization of the mRNA coding for glutamic acid decarboxylase (GAD) of MPTP monkeys showed a significant increase in the mean density of silver grains over every labelled neuron in the globus pallidum lateralis (56.8% over control) as well as the globus pallidus medialis (GPM) (45.7% over control) and the substantia nigra reticulata (SNR) (35.8% over control). No significant change was observed in the thalamic nucleus reticularis. Subthalamotomy (Groups C and D) produced a significant reduction in mRNA GAD expression on the side of the lesion in the GPM and the SNR (34% and 42.3%, respectively) with respect to the ipsilateral (non-lesioned) side and also when compared with parkinsonian monkeys. These results confirm and expand, at the cellular level, the paramount role of STN hyperactivity in the pathophysiology of parkinsonism. The therapeutic consequences of these findings for surgical treatment of Parkinson's disease are discussed.
19只食蟹猴被分为四组:A组(n = 3)为对照组;B组(n = 3),用1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的猴子;C组(n = 8),用MPTP处理且通过注射海人酸单侧损毁丘脑底核(STN)的动物;D组(n = 5),在给予MPTP之前损毁STN。丘脑底核切开术使C组猴子的震颤、自发活动、运动迟缓(通过手动运动测试评估)和冻结现象得到双侧改善。所有这些猴子均出现了与损伤对侧的偏身舞蹈症。这种改善持续存在,偏身舞蹈症一直持续到死亡。D组猴子表现出严重的偏身颤搐,在整个MPTP给药过程中持续存在,并主要在损伤同侧出现帕金森氏体征。对MPTP处理猴子的编码谷氨酸脱羧酶(GAD)的mRNA进行原位杂交分析显示,苍白球外侧(比对照组高56.8%)、苍白球内侧(GPM,比对照组高45.7%)和黑质网状部(SNR,比对照组高35.8%)中每个标记神经元上银颗粒的平均密度显著增加。丘脑网状核未观察到显著变化。与同侧(未损伤)侧相比,以及与帕金森氏症猴子相比,丘脑底核切开术(C组和D组)使GPM和SNR损伤侧的mRNA GAD表达显著降低(分别为34%和42.3%)。这些结果在细胞水平上证实并扩展了STN功能亢进在帕金森病病理生理学中的首要作用。讨论了这些发现对帕金森病手术治疗的治疗意义。