Maeda Fumiatsu, Kelbsch Carina, Straßer Torsten, Skorkovská Karolína, Peters Tobias, Wilhelm Barbara, Wilhelm Helmut
Pupil Research Group, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
Department of Orthoptics and Visual Sciences, Faculty of Medical Technology, Niigata University of Health and Welfare, Niigata, Japan.
Graefes Arch Clin Exp Ophthalmol. 2017 Sep;255(9):1837-1842. doi: 10.1007/s00417-017-3721-y. Epub 2017 Jun 30.
The pupil light reflex is considered to be a simple subcortical reflex. However, many studies have proven that patients with isolated occipital lesions with homonymous hemianopia show pupillary hemihypokinesia. Our hypothesis is that the afferent pupillary system consists of two pathways: one via intrinsically photosensitive retinal ganglion cells (ipRGCs), the other running through the normal RGCs via the visual cortex. The purpose of this study was to test the hypothesis of these two separate pupillomotor pathways.
12 patients (59.1 ± 18.8 years) with homonymous hemianopia due to post-geniculate lesions of the visual pathway and 20 normal controls (58.6 ± 12.9 years) were examined using chromatic pupillography: stimulus intensity was 28 lx corneal illumination, stimulus duration was 4.0 s, and the stimulus wavelengths were 420 ± 20 nm (blue) and 605 ± 20 nm (red), respectively. The examined parameters were baseline pupil diameter, latency, and relative amplitudes (absolute amplitudes compared to baseline), measured at maximal constriction, at 3 s after stimulus onset, at stimulus offset, and at 3 s and 7 s after stimulus offset.
The relative amplitudes for the red stimulus were significantly smaller for hemianopia patients compared to the normal controls [maximal constriction: 35.6 ± 5.9% (hemianopia) to 42.3 ± 5.7% (normal); p = 0.004; 3 s after stimulus onset: p = 0.004; stimulus offset: p = 0.001]. No significant differences in any parameter were found between the two groups using the blue stimulus.
The results support the hypothesis that the ipRGC pathway is mainly subcortical, whereas a second, non-ipRGC pathway via the occipital cortex exists.
瞳孔光反射被认为是一种简单的皮层下反射。然而,许多研究已证实,患有孤立性枕叶病变伴同侧偏盲的患者存在瞳孔半侧运动迟缓。我们的假设是,传入性瞳孔系统由两条通路组成:一条通过内在光敏性视网膜神经节细胞(ipRGCs),另一条通过视觉皮层经正常视网膜神经节细胞传导。本研究的目的是验证这两条独立瞳孔运动通路的假设。
对12例(年龄59.1±18.8岁)因视路膝状体后病变导致同侧偏盲的患者和20例正常对照者(年龄58.6±12.9岁)进行了彩色瞳孔描记术检查:刺激强度为角膜照明28勒克斯,刺激持续时间为4.0秒,刺激波长分别为420±20纳米(蓝色)和605±20纳米(红色)。所检测的参数包括基线瞳孔直径、潜伏期和相对幅度(与基线相比的绝对幅度),在最大收缩时、刺激开始后3秒、刺激结束时以及刺激结束后3秒和7秒进行测量。
与正常对照者相比,偏盲患者红色刺激的相对幅度明显较小[最大收缩时:35.6±5.9%(偏盲)对42.3±5.7%(正常);p = 0.004;刺激开始后3秒:p = 0.004;刺激结束时:p = 0.001]。两组使用蓝色刺激时,任何参数均未发现显著差异。
结果支持以下假设,即ipRGC通路主要是皮层下的,而经由枕叶皮层的第二条非ipRGC通路是存在的。