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移植物的植入以及纹状体内再支配的不均匀模式对于移植物诱导的运动障碍的发展很重要。

Graft placement and uneven pattern of reinnervation in the striatum is important for development of graft-induced dyskinesia.

作者信息

Carlsson Thomas, Winkler Christian, Lundblad Martin, Cenci M Angela, Björklund Anders, Kirik Deniz

机构信息

Wallenberg Neuroscience Center, Department of Experimental Medical Science, Lund University, BMC A11, 221 84, Lund, Sweden.

出版信息

Neurobiol Dis. 2006 Mar;21(3):657-68. doi: 10.1016/j.nbd.2005.09.008. Epub 2005 Oct 26.

Abstract

In two recent double-blind clinical trials of fetal ventral mesencephalic cell transplants into the striatum in patients with Parkinson's disease (PD), a significant proportion of the grafted patients developed dyskinetic side effects, which were not seen in the sham operated patients. Comparison between dyskinetic and non-dyskinetic grafted patients in one of the trials suggested that an uneven pattern of striatal reinnervation might be the leading cause of the dyskinesias. Here, we studied the importance of graft placement for the development of dyskinesias in parkinsonian rats. Abnormal involuntary movements resembling peak-dose dyskinesias seen in PD patients were induced by daily injections of L-DOPA for 6 weeks. The dyskinetic animals received about 130.000 fetal ventral mesencephalic cells as single grafts placement in the rostral or the caudal aspect of the head of striatum. The results show that grafts placed in the caudal, but not the rostral, part are effective in reducing the L-DOPA-induced limb and orolingual dyskinesia, predominantly seen as hyperkinesia. The same grafts, however, also induced a new type of dyskinetic behavior after activation with amphetamine, which were not seen in non-grafted lesion controls. The severity of these abnormal involuntary movements was significantly correlated with a higher graft-derived dopaminergic reinnervation in the caudal aspect of the head of striatum relative to the rostral part. The results indicate that graft-induced dyskinesias in PD patients may be linked to single, small graft deposits that provide an uneven, patchy reinnervation of the putamen.

摘要

在最近两项针对帕金森病(PD)患者进行的胎儿腹侧中脑细胞纹状体移植的双盲临床试验中,相当一部分接受移植的患者出现了运动障碍副作用,而假手术患者未出现这种情况。其中一项试验中对出现运动障碍和未出现运动障碍的移植患者进行比较,结果表明纹状体再支配模式不均衡可能是运动障碍的主要原因。在此,我们研究了移植部位对帕金森病大鼠运动障碍发生发展的重要性。通过每天注射左旋多巴6周,诱导出类似于PD患者峰值剂量运动障碍的异常不自主运动。出现运动障碍的动物接受了约130,000个胎儿腹侧中脑细胞,作为单个移植物分别植入纹状体头部的喙侧或尾侧。结果显示,植入尾侧而非喙侧的移植物能有效减轻左旋多巴诱导的肢体和口面部运动障碍,主要表现为运动亢进。然而,同样的移植物在使用苯丙胺激活后也会诱发一种新型的运动障碍行为,而未移植的损伤对照动物中未出现这种情况。这些异常不自主运动的严重程度与纹状体头部尾侧相对于喙侧更高的移植物源性多巴胺能再支配显著相关。结果表明,PD患者中移植物诱导的运动障碍可能与单个小移植物沉积有关,这些沉积导致壳核的再支配不均衡且呈斑片状。

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