Hussain Zahra, Svensson Carl-Magnus, Besle Julien, Webb Ben S, Barrett Brendan T, McGraw Paul V
School of Psychology, University of Nottingham, Nottingham, United Kingdom.
MRC Institute of Hearing Research, Nottingham, United Kingdom.
J Vis. 2015 Feb 26;15(2):25. doi: 10.1167/15.2.25.
We describe a method for deriving the linear cortical magnification factor from positional error across the visual field. We compared magnification obtained from this method between normally sighted individuals and amblyopic individuals, who receive atypical visual input during development. The cortical magnification factor was derived for each subject from positional error at 32 locations in the visual field, using an established model of conformal mapping between retinal and cortical coordinates. Magnification of the normally sighted group matched estimates from previous physiological and neuroimaging studies in humans, confirming the validity of the approach. The estimate of magnification for the amblyopic group was significantly lower than the normal group: by 4.4 mm deg(-1) at 1° eccentricity, assuming a constant scaling factor for both groups. These estimates, if correct, suggest a role for early visual experience in establishing retinotopic mapping in cortex. We discuss the implications of altered cortical magnification for cortical size, and consider other neural changes that may account for the amblyopic results.
我们描述了一种从视野中位置误差推导线性皮质放大因子的方法。我们比较了正常视力个体与弱视个体(后者在发育过程中接受非典型视觉输入)通过该方法获得的放大率。使用视网膜和皮质坐标之间已建立的共形映射模型,从视野中32个位置的位置误差为每个受试者推导皮质放大因子。正常视力组的放大率与先前人类生理和神经影像学研究的估计值相符,证实了该方法的有效性。弱视组的放大率估计值显著低于正常组:假设两组的缩放因子恒定,在偏心度为1°时低4.4 mm deg(-1)。这些估计值如果正确,表明早期视觉经验在建立皮质视网膜拓扑映射中起作用。我们讨论了皮质放大率改变对皮质大小的影响,并考虑了可能导致弱视的其他神经变化。