Gastinger Matthew J, Tian Ning, Horvath Tamas, Marshak David W
Graduate School of Biomedical Sciences, The University of Texas Health Science Center Houston, Houston, Texas 77225, USA.
Curr Eye Res. 2006 Jul-Aug;31(7-8):655-67. doi: 10.1080/02713680600776119.
Since 1892, anatomical studies have demonstrated that the retinas of mammals, including humans, receive input from the brain via axons emerging from the optic nerve. There are only a small number of these retinopetal axons, but their branches in the inner retina are very extensive. More recently, the neurons in the brain stem that give rise to these axons have been localized, and their neurotransmitters have been identified. One set of retinopetal axons arises from perikarya in the posterior hypothalamus and uses histamine, and the other arises from perikarya in the dorsal raphe and uses serotonin. These serotonergic and histaminergic neurons are not specialized to supply the retina; rather, they are a subset of the neurons that project via collaterals to many other targets in the central nervous system, as well. They are components of the ascending arousal system, firing most rapidly when the animal is awake and active. The contributions of these retinopetal axons to vision may be predicted from the known effects of serotonin and histamine on retinal neurons. There is also evidence suggesting that retinopetal axons play a role in the etiology of retinal diseases.
自1892年以来,解剖学研究表明,包括人类在内的哺乳动物的视网膜通过视神经发出的轴突接收来自大脑的输入。这些向视网膜投射的轴突数量很少,但它们在内层视网膜中的分支非常广泛。最近,产生这些轴突的脑干神经元已被定位,并且它们的神经递质已被确定。一组向视网膜投射的轴突起源于下丘脑后部的神经细胞体,使用组胺,另一组起源于中缝背核的神经细胞体,使用血清素。这些血清素能和组胺能神经元并非专门为供应视网膜而存在;相反,它们是通过侧支投射到中枢神经系统许多其他靶点的神经元的一个子集。它们是上行唤醒系统的组成部分,在动物清醒和活跃时放电最快。这些向视网膜投射的轴突对视觉的贡献可以从血清素和组胺对视网膜神经元的已知作用中预测出来。也有证据表明,向视网膜投射的轴突在视网膜疾病的病因学中起作用。