Matthews M A, West L C, Clarkson D B
Neuroscience. 1982 Feb;7(2):385-404. doi: 10.1016/0306-4522(82)90274-3.
Developmental alterations in the amount of tritiated proline and fucose incorporated by retinal neurons and transported within axons of the optic nerve to the dorsal lateral geniculate nucleus and superior colliculus were measured at 1, 5, 10 and 15 days postnatal using quantitative autoradiography and liquid scintillation analysis. The amount of axon transport inhibition induced by introacular injections of colchicine (10-4 M-5 X 10-3M) and xylocaine (10-3 M-10-1 M) was also determined by this methodology. Grain counts of retinal autoradiograms obtained from animals of all ages employed in this study demonstrated that [3H] proline is rapidly incorporated by all retinal neurons but becomes increasingly concentrated within the inner nuclear, ganglion cell and optic fiber layers between 2h and 2 days after injection. [3H] fucose is preferentially taken up and concentrated within the plexiform and sensory element layers. Intraocular colchicine administered 24 h prior to isotope injection exhibited no significant effect on incorporation but depressed the amount of activity in the layer of optic fibers. Comparison of the effects of colchicine and xylocaine on axon transport of [3H] proline injected at 3 days of age revealed dose-dependent suppression of transport occurring up to six hr after isotope injection; however, with longer survival periods the effects of xylocaine were no longer significant whereas colchicine maintained suppression of axon transport to 20% of normal for periods of up to 10 days. Additionally, the rate and quantity of 3H] proline transported to the dorsal lateral geniculate nucleus and tectum of 1-15 day old animals was found to be inversely proportional to the age of the animal. Maximally-effective concentrations of colchicine, determined for each age level examined by the previous study to be highest compatible with the viability of the retino-fugal projection, 34 also reduced transport to from 20-40% of normal, being most effective in animals of 1-10 days of age. Autoradiographs of the optic disc demonstrated a colchicine-induced suppression of the amount of label in the exiting optic fibers and similar preparations of the tectum revealed an elimination of activity in the stratum griseum superficialis and stratum opticum which are normally heavily labeled following intraocular [3H] proline or fucose. Following [3H] fucose injection at 10 days of age, isotope appears in the contralateral visual cortex between 3 and 10 days later, indicating a substantial amount of transneuronal transfer of label which appeared to occur in concert with periods of maximal synaptogenesis. Injection of colchicine reduced the amount of label in the cortex to background levels. Concomitantly, autoradiographs of the dorsal lateral geniculate nucleus revealed cytoplasmic labeling of geniculate neurons in control animals but this was eliminated following colchicine injection...
在出生后1、5、10和15天,采用定量放射自显影和液体闪烁分析技术,测量视网膜神经元摄取并在视神经轴突内运输到背外侧膝状核和上丘的氚化脯氨酸和岩藻糖的量的发育变化。通过该方法还确定了眼内注射秋水仙碱(10-4M - 5×10-3M)和利多卡因(10-3M - 10-1M)诱导的轴突运输抑制量。从本研究中使用的所有年龄段动物获得的视网膜放射自显影片的颗粒计数表明,[3H]脯氨酸被所有视网膜神经元迅速摄取,但在注射后2小时至2天内,在内核层、神经节细胞层和视神经纤维层中浓度越来越高。[3H]岩藻糖优先被摄取并集中在神经丛和感觉元件层中。在同位素注射前24小时给予眼内秋水仙碱对摄取没有显著影响,但降低了视神经纤维层中的活性量。比较秋水仙碱和利多卡因对3日龄注射的[3H]脯氨酸轴突运输的影响,发现同位素注射后长达6小时出现剂量依赖性的运输抑制;然而,随着存活时间延长,利多卡因的影响不再显著,而秋水仙碱在长达10天的时间内将轴突运输抑制维持在正常水平的20%。此外,发现1 - 15日龄动物运输到背外侧膝状核和顶盖的[3H]脯氨酸的速率和量与动物年龄成反比。通过先前研究确定的每个年龄水平的秋水仙碱最大有效浓度,与视网膜-视束投射的存活能力最相容,也将运输降低到正常水平的20 - 40%,在1 - 10日龄的动物中最有效。视盘的放射自显影片显示秋水仙碱诱导的出射视神经纤维中标记量的抑制,顶盖的类似制剂显示浅灰色层和视神经层中的活性消除,而眼内注射[3H]脯氨酸或岩藻糖后这些层通常被大量标记。在10日龄注射[3H]岩藻糖后,同位素在3至10天后出现在对侧视觉皮层中,表明大量的标记跨神经元转移似乎与最大突触发生期同时发生。注射秋水仙碱将皮层中的标记量降低到背景水平。同时,背外侧膝状核的放射自显影片显示对照动物中膝状神经元的细胞质标记,但秋水仙碱注射后这种标记消失……