Evidence for My-cell Involvement in the Spatial Frequency Doubled Illusion as Revealed by a Multiple Region PERG for Glaucoma

A. James, T. Maddess, K. Rouhan, S. Bedford, M. Snowball
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引用次数: 12

Abstract

Recent evidence suggests that glaucoma leads to early loss of large retinal ganglion cells1,2 projecting to the Magnocellular layers of the dLGN: the so called "M" retinal ganglion cells. It is necessary for the present study, to appreciate that there are two subgroups of M-cells, the Mx-cells which are quite linear, and the nonlinearly responding My-cells, where the subscripts indicate physiological similarities with cat X and Y-cells3. In particular the retinal gain control described by Shapley and Victor4 for cat X and Y cells is strongly expressed in primate M- cells5. Except at very low temporal frequencies the quadratic response of Y-cells is larger than the linear response, especially at low spatial frequencies6, and the gain control effects Y-cells more, especially their quadratic response7. At least three studies indicate that My-cells are larger than Mx- cells8,9,10. Therefore, methods for glaucoma diagnosis should perhaps appeal to My-cell physiology, e.g. the strong effects of gain control upon their nonlinear responses.
青光眼的多区PERG显示我细胞参与空间频率加倍错觉的证据
最近的证据表明,青光眼导致早期大视网膜神经节细胞1,2的丢失,这些细胞突出到dLGN的大细胞层,即所谓的“M”视网膜神经节细胞。在目前的研究中,有必要认识到m细胞有两个亚群,具有相当线性的mx细胞和非线性响应的my细胞,其中下标表示与cat X和y细胞的生理相似性。特别是Shapley和Victor4描述的猫X和Y细胞的视网膜增益控制在灵长类动物M-细胞中强烈表达。除了在极低的时间频率下,y -单元的二次响应大于线性响应,特别是在低空间频率下,增益控制对y -单元的影响更大,尤其是它们的二次响应。至少有三项研究表明,my细胞比Mx细胞大8,9,10。因此,青光眼的诊断方法可能会吸引My-cell生理学,例如增益控制对其非线性反应的强烈影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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