Smit A E, van der Geest J N, Vellema M, Koekkoek S K E, Willemsen R, Govaerts L C P, Oostra B A, De Zeeuw C I, VanderWerf F
Department of Neuroscience, Erasmus MC, Rotterdam, The Netherlands.
Genes Brain Behav. 2008 Oct;7(7):770-7. doi: 10.1111/j.1601-183X.2008.00417.x. Epub 2008 Jun 30.
The fragile X syndrome (FRAXA) is the most widespread heritable form of mental retardation caused by the lack of expression of the fragile X mental retardation protein (FMRP). This lack has been related to deficits in cerebellum-mediated acquisition of conditioned eyelid responses in individuals with FRAXA. In the present behavioral study, long-term effects of deficiency of FMRP were investigated by examining the acquisition, savings and extinction of delay eyeblink conditioning in male individuals with FRAXA. In the acquisition experiment, subjects with FRAXA displayed a significantly poor performance compared with controls. In the savings experiment performed at least 6 months later, subjects with FRAXA and controls showed similar levels of savings of conditioned responses. Subsequently, extinction was faster in subjects with FRAXA than in controls. These findings confirm that absence of the FMRP affects cerebellar motor learning. The normal performance in the savings experiment and aberrant performance in the acquisition and extinction experiments of individuals with FRAXA suggest that different mechanisms underlie acquisition, savings and extinction of cerebellar motor learning.
脆性X综合征(FRAXA)是由脆性X智力低下蛋白(FMRP)表达缺失引起的最常见的遗传性智力障碍形式。这种缺失与FRAXA患者小脑介导的条件性眼睑反应习得缺陷有关。在本行为学研究中,通过检查患有FRAXA的男性个体延迟眨眼条件反射的习得、节省和消退情况,研究了FMRP缺乏的长期影响。在习得实验中,与对照组相比,患有FRAXA的受试者表现明显较差。在至少6个月后进行的节省实验中,患有FRAXA的受试者和对照组表现出相似水平的条件反应节省。随后,患有FRAXA的受试者的消退比对照组更快。这些发现证实FMRP的缺失会影响小脑运动学习。FRAXA患者在节省实验中的正常表现以及在习得和消退实验中的异常表现表明,小脑运动学习的习得、节省和消退存在不同的机制。