Bonaventure N, Wioland N, Karli P
Doc Ophthalmol. 1985 Oct 30;61(1):97-103. doi: 10.1007/BF00143221.
The rd/rd mutation provokes a specific degeneration of the photoreceptive cells in the mouse retina, without affecting other neuronal elements. This degeneration starts 8 to 10 days after birth. Discriminative learning experiments have shown the degenerated retina to remain light-sensitive, the sensitivity being reduced to 10(-5) of normal with a peak still at 500 nm. An ontogenetic study showed a progressive vanishing of visual potentials (electroretinogram and visual evoked potentials) during the third week of life. Potentials of auditory origin, which can be recorded from the visual cortex in normal mice, were found to be clearly facilitated by the absence of the visual input either because of retinal degeneration in rd mouse or provoked by enucleation at birth.
rd/rd突变引发小鼠视网膜光感受器细胞的特异性退化,而不影响其他神经元成分。这种退化在出生后8至10天开始。辨别学习实验表明,退化的视网膜仍对光敏感,其敏感度降至正常的10^(-5),峰值仍在500纳米处。一项个体发育研究表明,在出生后的第三周,视觉电位(视网膜电图和视觉诱发电位)逐渐消失。在正常小鼠中可从视觉皮层记录到的听觉起源电位,被发现因rd小鼠的视网膜退化或出生时摘除眼球导致视觉输入缺失而明显增强。