Hess Robert F, Thompson Benjamin, Gole Glen, Mullen Kathy T
McGill Vision Research (H4.14), Department of Ophthalmology, McGill University, 687 Pine Avenue West, Montreal, QC H3A1A1, Canada.
Eur J Neurosci. 2009 Mar;29(5):1064-70. doi: 10.1111/j.1460-9568.2009.06650.x.
Amblyopia or lazy eye is the most common cause of uniocular blindness in adults. It is caused by a disruption to normal visual development as a consequence of unmatched inputs from the two eyes in early life, arising from a turned eye (strabismus), unequal refractive error (anisometropia) or form deprivation (e.g. cataract). Animal models based on extracellular recordings in anesthetized animals suggest that the earliest site of the anomaly in the primate visual pathway is the primary visual cortex (corresponding to the striate cortex, cytoarchitectonic area 17 and area V1), which is where inputs from the two eyes are first combined in an excitatory fashion, whereas more distal and monocular processing structures such as the retina and lateral geniculate nucleus (LGN) are normal. Using high-field functional magnetic resonance imaging in a group of human adults with amblyopia, we demonstrate that functional deficits are first observable at a thalamic level, that of the LGN. Our results suggest the need to re-evaluate the current models of amblyopia that are based on the assumption of a purely cortical dysfunction, as well as the role for the LGN in visual development.
弱视或懒眼症是成人单眼失明的最常见原因。它是由于早年双眼输入不匹配导致正常视觉发育中断引起的,这种不匹配源于斜视、屈光参差(两眼屈光不正度数不同)或形觉剥夺(如白内障)。基于对麻醉动物进行细胞外记录的动物模型表明,灵长类视觉通路中最早出现异常的部位是初级视觉皮层(对应于纹状皮层、细胞构筑区17和V1区),在这里来自两眼的输入首先以兴奋性方式组合,而更远端的单眼处理结构如视网膜和外侧膝状体核(LGN)则是正常的。我们对一组患有弱视的成年人类使用高场功能磁共振成像,证明功能缺陷首先在丘脑水平(即LGN)上可观察到。我们的结果表明,需要重新评估当前基于纯皮层功能障碍假设的弱视模型,以及LGN在视觉发育中的作用。