De Nardis R, Sattayasai J, Zappia J, Ehrlich D
Department of Anatomy, Monash University, Clayton, Vic., Australia.
Dev Neurosci. 1988;10(4):256-69. doi: 10.1159/000111976.
The neurotoxic effects of kainic acid (KA) on developing neurons in the chick retina was investigated in an in vitro preparation. Eyecups from chick embroyos at 6 (E-6), 8, 10, 12, 14, 16, and 20 days of incubation and from chicks on day 1 posthatch (D-1) were exposed to different doses of KA for 30 min and then processed for light microscopy. Neurotoxic damage was evaluated by the presence of swollen cell bodies, containing pale cytoplasm and pyknotic nuclei. At E-8, amacrine cells first became sensitive to KA and displayed neurotoxic damage at a threshold concentration of 20 microM. Their sensitivity to KA increased over the following 4 days, so that by E-12 they attained a threshold sensitivity of 5.0 microM KA. At E-14, one third of the retinae showed amacrine cell damage at 0.5-2.0 microM KA, less than the threshold dose of 5.0 microM KA required at D-1. Bipolar cells first become sensitive to KA at E-12, at a threshold concentration of 5.0 microM. The threshold concentration decreased over the following 10 days: 2.0 microM at E-16, 1.0 microM at E-20, and 0.5 microM at D-1. At E-8 and E-10, horizontal cells were susceptible to a relatively high concentration of 80 microM KA. The sensitivity to KA is evident prior to the formation of photoreceptor input. These results indicate that amacrine and horizontal cells are susceptible to KA at an earlier age than bipolar cells. Both amacrine and bipolar cells exhibit an age-dependent relationship with the threshold concentration of KA required to cause neurotoxicity; in general, the older the embryo, the lower the dose of KA. However, the increased susceptibility of amacrine cells at E-14 suggests a transient hypersensitivity to KA during this period which may reflect an overproduction of the receptor-ionic channel complex necessary for KA to exert its effect.
在体外实验中研究了红藻氨酸(KA)对雏鸡视网膜发育中神经元的神经毒性作用。将孵化6(E - 6)、8、10、12、14、16和20天的鸡胚以及出壳后第1天(D - 1)雏鸡的眼杯暴露于不同剂量的KA中30分钟,然后进行光学显微镜检查。通过出现含有淡染细胞质和固缩核的肿胀细胞体来评估神经毒性损伤。在E - 8时,无长突细胞首先对KA变得敏感,并在20微摩尔的阈值浓度下表现出神经毒性损伤。在接下来的4天里,它们对KA的敏感性增加,到E - 12时,它们达到了5.0微摩尔KA的阈值敏感性。在E - 14时,三分之一的视网膜在0.5 - 2.0微摩尔KA时出现无长突细胞损伤,低于D - 1时所需的5.0微摩尔KA的阈值剂量。双极细胞在E - 12时首先对KA变得敏感,阈值浓度为5.0微摩尔。在接下来的10天里,阈值浓度降低:E - 16时为2.0微摩尔,E - 20时为1.0微摩尔,D - 1时为0.5微摩尔。在E - 8和E - 10时,水平细胞对相对较高浓度的80微摩尔KA敏感。在光感受器输入形成之前,对KA的敏感性就很明显。这些结果表明,无长突细胞和水平细胞比双极细胞在更早的年龄就易受KA影响。无长突细胞和双极细胞与引起神经毒性所需的KA阈值浓度均呈现年龄依赖性关系;一般来说,胚胎年龄越大,KA的剂量越低。然而,E - 14时无长突细胞敏感性增加表明在此期间对KA有短暂的超敏反应,这可能反映了KA发挥作用所需的受体 - 离子通道复合物的过度产生。