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突变体视觉缺陷的行为评估。

Behavioral assessment of visual deficits in the mutant.

作者信息

Bloom C M, Post R J, Anch A M, Davenport D G

机构信息

Department of Psychology,

Department of Biology, Providence College, Providence, RI, USA.

出版信息

Degener Neurol Neuromuscul Dis. 2013 May 9;3:15-21. doi: 10.2147/DNND.S44064. eCollection 2013.

Abstract

(tremor, ataxia, immobility, epilepsy, paralysis) mutants show a significant increase in myelin thickness from 10 to 30 days of age but then demonstrate a decrease in myelin thickness from 1 to 6 months. The severity of the demyelination in the optic nerve suggests that visual deficits may exist in the mutants. Animals were trained on a discrimination task, in which responses to a light stimulus (the S period) were reinforced on a fixed ratio (FR)-1 schedule, and responses in the absence of the light stimulus (the S period) were not reinforced. Following training, the light intensity presented during the S period was gradually reduced between sessions until -6.0 candela/m was reached. Both groups of animals - mutants and control Sprague Dawley rats - successfully recognized and responded in the presence of the stimulus near perfectly by the final day of training, suggesting that mutants demonstrated normal learning, at least under this paradigm. Despite the severe demyelination of the optic nerve, no visual deficits were detected as both groups of animals performed similarly as the light intensity decreased. Though the myelin loss of the optic nerve may have negatively affected signal transduction, this did not result in an increase in visual threshold.

摘要

(震颤、共济失调、运动不能、癫痫、麻痹)突变体在10至30日龄时髓鞘厚度显著增加,但在1至6个月时髓鞘厚度则下降。视神经脱髓鞘的严重程度表明突变体可能存在视觉缺陷。动物接受辨别任务训练,在该任务中,对光刺激(S期)的反应按固定比率(FR)-1时间表得到强化,而在无光刺激(非S期)时的反应则不被强化。训练后,各训练阶段之间S期呈现的光强度逐渐降低,直至达到-6.0坎德拉/平方米。两组动物——突变体和对照斯普拉格-道利大鼠——在训练的最后一天,在刺激出现时几乎都能成功识别并做出近乎完美的反应,这表明突变体至少在这种范式下表现出正常的学习能力。尽管突变体的视神经存在严重脱髓鞘,但随着光强度降低,两组动物表现相似,未检测到视觉缺陷。虽然视神经的髓鞘损失可能对视信号转导产生了负面影响,但这并未导致视觉阈值升高。

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Behavioral assessment of visual deficits in the mutant.突变体视觉缺陷的行为评估。
Degener Neurol Neuromuscul Dis. 2013 May 9;3:15-21. doi: 10.2147/DNND.S44064. eCollection 2013.

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