Trejo L J, Cicerone C M
Brain Res. 1984 May 21;300(1):49-62. doi: 10.1016/0006-8993(84)91340-4.
Extracellular microelectrode recordings from 148 single cells in the pretectum of the hooded rat were classified according to their temporal response properties to light stimulation of their retinal receptive fields. Fifty-six cells were classified as tonic-on cells, 22 cells were classified as tonic-off cells, and 53 cells were classified as phasic cells. Seventeen cells could not be assigned to one of these 3 groups. The diameters of the receptive field centers of the tonic-on pretectal cell were clustered about a mean of 31 degrees and the temporal response of these cells was sustained. Constriction of the contralateral pupil was produced by electrical stimulation through the recording electrode at sites containing tonic-on pretectal cells, but not at sites containing tonic-off pretectal cells or phasic pretectal cells. For this reason, we argue that tonic-on cells are likely to mediate constriction in the light reflex of the rat's pupil. Receptive field maps together with electrolytic marking lesions at recording and stimulation sites showed that tonic-on pretectal cells are retinotopically organized and are aggregated in a strip running from the dorso-medial tip of the pretectum to the ventro-lateral boundary. The anatomical distribution of these cells is coextensive with the region known as the pretectal olivary nucleus (PO) in the rat. Using fine microelectrodes, recordings were obtained from 27 axons presumed to be of optic origin (fibers). Of these, 14 were tonic-on, 10 were phasic, 2 were tonic-off, and 2 were unclassified. Recordings from tonic-on fibers were obtained near tonic-on pretectal cells, typically in the most dorsal light-responsive region of the pretectum. These fibers were activated by single pulse electrical stimulation of the optic chiasm. The mean receptive field center diameter of 6 tonic-on fibers was 10.1 degrees, or about a factor of 3 less than that of pretectal tonic-on cells. The mean conduction velocity of 14 tonic-on fibers was 3.1 m/s. We argue that the tonic-on cells of the PO serve to integrate signals from tonic-on center retinal ganglion cells with adjacent receptive fields to provide signals for constriction of the pupil to neurons in the oculomotor nucleus.
对148个来自长爪沙鼠顶盖前区单细胞的细胞外微电极记录,根据其对视网膜感受野光刺激的时间反应特性进行分类。56个细胞被分类为紧张性开细胞,22个细胞被分类为紧张性关细胞,53个细胞被分类为相位性细胞。17个细胞无法归入这3组中的任何一组。紧张性开顶盖前区细胞的感受野中心直径集中在平均31度左右,这些细胞的时间反应是持续的。通过记录电极在含有紧张性开顶盖前区细胞的部位进行电刺激可引起对侧瞳孔收缩,但在含有紧张性关顶盖前区细胞或相位性顶盖前区细胞的部位则不会。因此,我们认为紧张性开细胞可能介导大鼠瞳孔光反射中的收缩。感受野图谱以及记录和刺激部位的电解标记损伤表明,紧张性开顶盖前区细胞呈视网膜拓扑组织,并聚集在一条从顶盖前区背内侧尖端延伸至腹外侧边界的条带中。这些细胞的解剖分布与大鼠中称为顶盖前橄榄核(PO)的区域范围一致。使用精细微电极,从27条推测为视源(纤维)的轴突上获得了记录。其中,14条为紧张性开,10条为相位性,2条为紧张性关,2条未分类。在紧张性开顶盖前区细胞附近获得了紧张性开纤维的记录,通常在顶盖前区最背侧的光反应区域。这些纤维通过视交叉的单脉冲电刺激而被激活。6条紧张性开纤维的平均感受野中心直径为10.1度,约为顶盖前区紧张性开细胞的三分之一。14条紧张性开纤维的平均传导速度为3.1米/秒。我们认为PO的紧张性开细胞用于整合来自具有相邻感受野的紧张性开中心视网膜神经节细胞的信号,为动眼神经核中的神经元提供瞳孔收缩信号。