成年小鼠单眼剥夺增强视力
Enhancement of vision by monocular deprivation in adult mice.
作者信息
Prusky Glen T, Alam Nazia M, Douglas Robert M
机构信息
Department of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
出版信息
J Neurosci. 2006 Nov 8;26(45):11554-61. doi: 10.1523/JNEUROSCI.3396-06.2006.
Plasticity of vision mediated through binocular interactions has been reported in mammals only during a "critical" period in juvenile life, wherein monocular deprivation (MD) causes an enduring loss of visual acuity (amblyopia) selectively through the deprived eye. Here, we report a different form of interocular plasticity of vision in adult mice in which MD leads to an enhancement of the optokinetic response (OKR) selectively through the nondeprived eye. Over 5 d of MD, the spatial frequency sensitivity of the OKR increased gradually, reaching a plateau of approximately 36% above pre-deprivation baseline. Eye opening initiated a gradual decline, but sensitivity was maintained above pre-deprivation baseline for 5-6 d. Enhanced function was restricted to the monocular visual field, notwithstanding the dependence of the plasticity on binocular interactions. Activity in visual cortex ipsilateral to the deprived eye was necessary for the characteristic induction of the enhancement, and activity in visual cortex contralateral to the deprived eye was necessary for its maintenance after MD. The plasticity also displayed distinct learning-like properties: Active testing experience was required to attain maximal enhancement and for enhancement to persist after MD, and the duration of enhanced sensitivity after MD was extended by increasing the length of MD, and by repeating MD. These data show that the adult mouse visual system maintains a form of experience-dependent plasticity in which the visual cortex can modulate the normal function of subcortical visual pathways.
通过双眼相互作用介导的视觉可塑性仅在幼年哺乳动物的“关键”时期被报道过,在此期间,单眼剥夺(MD)会通过被剥夺的眼睛选择性地导致视力持久丧失(弱视)。在此,我们报道成年小鼠中一种不同形式的双眼间视觉可塑性,其中MD会通过未被剥夺的眼睛选择性地增强视动反应(OKR)。在MD的5天时间里,OKR的空间频率敏感性逐渐增加,达到比剥夺前基线高出约36%的平台期。睁眼引发了逐渐下降,但敏感性在5 - 6天内维持在剥夺前基线之上。尽管可塑性依赖于双眼相互作用,但增强的功能仅限于单眼视野。被剥夺眼同侧视觉皮层的活动对于增强特征性诱导是必要的,而被剥夺眼对侧视觉皮层的活动对于MD后其维持是必要的。这种可塑性还表现出明显的类似学习的特性:需要主动测试经验才能达到最大增强,并且在MD后增强才能持续,并且通过增加MD的长度以及重复MD,可以延长MD后增强敏感性的持续时间。这些数据表明成年小鼠视觉系统维持着一种经验依赖性可塑性形式,其中视觉皮层可以调节皮层下视觉通路的正常功能。