Garthwaite J, Wilkin G P
Neuroscience. 1982 Oct;7(10):2499-514. doi: 10.1016/0306-4522(82)90210-x.
The neurotoxic actions of kainate were examined in incubated slices of adult and immature rat cerebellum using light- and electron-microscopy. In the adult, Purkinje cells and inhibitory interneurones became selectively necrotic at concentrations between 5 micro M and 20 micro M. At 30 micro M, granule cells also became affected. In the immature cerebellum, at an age (8 days after birth) when the parallel fibres (thought to use glutamate as transmitter) are largely yet to be developed, selective toxicity was still evident but Purkinje cells and inhibitory interneurones were about 10-fold, and granule cells about 30-fold, less sensitive to kainate than in the adult. Kainate and other excitotoxins also increased cyclic GMP levels in cerebellar slices, apparently through the activation of excitatory amino acid receptors. In the adult tissue, the dose-cyclic GMP response curve to kainate was biphasic suggesting the presence of two components. The lower concentrations of kainate eliciting the first component mirrored those inducing selective necrosis of Purkinje cells and inhibitory interneurones while the second component correlated with necrosis of granule cells. Similar correlations applied to the immature cerebellum, but here kainate neurotoxicity appeared to be associated with the activation of receptor types different from those evident in the adult. It is suggested that kainate receptors, whose activation is associated with both neurotoxic damage and elevation of cyclic GMP levels, are located on all cell types in the adult cerebellum, with Purkinje cells and inhibitory interneurones displaying a higher sensitivity to kainate than granule cells. The lower sensitivity of immature cerebellum to the neurotoxic effect of kainate is probably due to lower levels of kainate receptors.
利用光学显微镜和电子显微镜,研究了成年和未成熟大鼠小脑孵育切片中红藻氨酸的神经毒性作用。在成年大鼠中,当浓度在5微摩尔至20微摩尔之间时,浦肯野细胞和抑制性中间神经元会选择性坏死。在30微摩尔时,颗粒细胞也会受到影响。在未成熟小脑中,在出生后8天这个年龄,平行纤维(被认为以谷氨酸作为递质)大部分尚未发育,选择性毒性仍然明显,但浦肯野细胞和抑制性中间神经元对红藻氨酸的敏感性比成年大鼠低约10倍,颗粒细胞则低约30倍。红藻氨酸和其他兴奋性毒素还会增加小脑切片中的环磷酸鸟苷水平,显然是通过激活兴奋性氨基酸受体实现的。在成年组织中,红藻氨酸的剂量-环磷酸鸟苷反应曲线呈双相,表明存在两个成分。引发第一成分的较低浓度红藻氨酸与诱导浦肯野细胞和抑制性中间神经元选择性坏死的浓度相似,而第二成分与颗粒细胞坏死相关。类似的相关性也适用于未成熟小脑,但在这里,红藻氨酸神经毒性似乎与不同于成年大鼠中明显的受体类型的激活有关。有人提出,其激活与神经毒性损伤和环磷酸鸟苷水平升高均相关的红藻氨酸受体,位于成年小脑的所有细胞类型上,浦肯野细胞和抑制性中间神经元对红藻氨酸的敏感性高于颗粒细胞。未成熟小脑对红藻氨酸神经毒性作用的较低敏感性可能是由于红藻氨酸受体水平较低。