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通过中央和周边光谱敏感度差异得出的黄斑色素密度。

Macular pigment densities derived from central and peripheral spectral sensitivity differences.

作者信息

Sharpe L T, Stockman A, Knau H, Jägle H

机构信息

Forschungsstelle für Experimentelle Ophthalmologie, Universitäts-Augenklinik, Tübingen, Germany.

出版信息

Vision Res. 1998 Nov;38(21):3233-9. doi: 10.1016/s0042-6989(97)00457-4.

DOI:10.1016/s0042-6989(97)00457-4
PMID:9893831
Abstract

Estimates of the density spectrum of the macular pigment (Wyszecki G, Stiles WS. Color Science: Concepts and Methods. Quantitative Data and Formulas. 1st ed. New York: Wiley, 1967); (Vos JJ. Literature review of human macular absorption in the visible and its consequences for the cone receptor primaries. Institute for Perception. Soesterberg, The Netherlands, 1972) are partially based on the difference between central and peripheral spectral sensitivities, measured under conditions chosen to isolate a single cone class (Stiles WS. Madrid: Union Internationale de Physique Pure et Appliquée, 1953;1:65-103). Such derivations assume that the isolated spectral sensitivity is the same at both retinal locations, save for the intervening macular pigment. If this is true, then the type of cone class mediating detection should not influence the calculated difference spectrum. To test this assumption, we measured central and peripheral spectral sensitivities in a deuteranope, a protanope and a normal trichromat observer: (a) for short-wave sensitive (S-) cone detection; and (b) for long-wave sensitive (L-) cone detection (deuteranope), for middle-wave sensitive (M-) cone detection (protanope) or for both L- and M-cone detection (normal trichromat). The difference spectra determined for L- or M-cone detection deviate significantly from those measured for S-cone detection, at wavelengths below 450 nm. A theoretical analysis suggests that the discrepancies are owing, in part, to regional variation in the optical density of the cone pigments; and that such receptor variation cannot be ignored when deriving the standard density spectrum of the macular pigment.

摘要

黄斑色素密度光谱的估计值(Wyszecki G, Stiles WS.《颜色科学:概念与方法、定量数据和公式》第1版。纽约:威利出版社,1967年);(Vos JJ. 关于人眼黄斑在可见光下的吸收及其对视锥细胞原色影响的文献综述。荷兰索斯特贝格感知研究所,1972年)部分基于在选择分离单一视锥细胞类型的条件下测量的中央和周边光谱敏感度之间的差异(Stiles WS. 马德里:国际纯粹与应用物理联合会,1953年;1:65 - 103)。此类推导假设,除了中间的黄斑色素外,在两个视网膜位置分离出的光谱敏感度是相同的。如果这是真的,那么介导检测的视锥细胞类型不应影响计算出的差异光谱。为了检验这一假设,我们在一名绿色盲患者、一名红色盲患者和一名正常三色视觉观察者中测量了中央和周边光谱敏感度:(a) 用于短波敏感(S)视锥细胞检测;以及 (b) 用于长波敏感(L)视锥细胞检测(绿色盲患者)、中波敏感(M)视锥细胞检测(红色盲患者)或L和M视锥细胞检测(正常三色视觉观察者)。在波长低于450 nm时,针对L或M视锥细胞检测确定的差异光谱与针对S视锥细胞检测测量的差异光谱有显著偏差。理论分析表明,这些差异部分归因于视锥细胞色素光密度的区域变化;并且在推导黄斑色素的标准密度光谱时,这种受体变化不能被忽略。

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