Baroncelli Laura, Maffei Lamberto, Sale Alessandro
Institute of Neuroscience, National Research Council Pisa, Italy.
Front Cell Neurosci. 2011 Nov 24;5:25. doi: 10.3389/fncel.2011.00025. eCollection 2011.
Amblyopia is the most common form of impairment of visual function affecting one eye, with a prevalence of about 1-5% of the total world population. This pathology is caused by early abnormal visual experience with a functional imbalance between the two eyes owing to anisometropia, strabismus, or congenital cataract, resulting in a dramatic loss of visual acuity in an apparently healthy eye and various other perceptual abnormalities, including deficits in contrast sensitivity and in stereopsis. It is currently accepted that, due to a lack of sufficient plasticity within the brain, amblyopia is untreatable in adulthood. However, recent results obtained both in clinical trials and in animal models have challenged this traditional view, unmasking a previously unsuspected potential for promoting recovery after the end of the critical period for visual cortex plasticity. These studies point toward the intracortical inhibitory transmission as a crucial brake for therapeutic rehabilitation and recovery from amblyopia in the adult brain.
弱视是影响单眼的最常见视觉功能障碍形式,全球总患病率约为1%-5%。这种病症是由早期异常视觉体验引起的,由于屈光参差、斜视或先天性白内障导致双眼之间功能失衡,从而使一只看似健康的眼睛视力急剧下降,并出现各种其他感知异常,包括对比敏感度和立体视功能缺陷。目前普遍认为,由于大脑缺乏足够的可塑性,弱视在成年后无法治疗。然而,最近在临床试验和动物模型中获得的结果对这一传统观点提出了挑战,揭示了在视觉皮层可塑性关键期结束后促进恢复的先前未被怀疑的潜力。这些研究表明,皮质内抑制性传递是成人大脑弱视治疗康复和恢复的关键阻碍。