Coyle J T, Molliver M E, Kuhar M J
J Comp Neurol. 1978 Jul 15;180(2):301-23. doi: 10.1002/cne.901800208.
The morphologic sequelae following stereotaxic injection into the rat striatum of kainic acid, a conformationally restricted analogue of glutamate, were examined by means of bright field, histofluorescence and electron microscopic techniques. The neuropathologic response to kainate injection occurs in two distinct phases. First, the intrinsic neurons of the striatum undergo a rapid degeneration during the first 48 hours after injection; this is characterized by the sequential loss of cytoplasmic Nissl-substance (chromatolysis), shrinkage of the perikarya, clumping of the nuclear chromatin and finally disruption of the nuclear membrane. Between one and three weeks after injection, a marked proliferation of astrocytes in the gray matter formerly populated by neurons characterizes the second phase. The region of several neuronal loss in the kainate injected striatum is approximately spherical in shape, and its extent is non-linearly related to the amount of kainate injected. The neuropil of the injected striatum is markedly disrupted due to the death of intrinsic neurons and loss of their processes. Yet, histofluorescence microscopy demonstrates that the dopaminergic axons projecting from the substantia nigra do not degenerate in the kainate injected striatum; electron microscope studies indicate that corticofugal fibers traversing the striatum are also unaffected by kainate. Many presynaptic boutons, presumably of extrinsic origin, are intact up to ten days after injection; osmophilic vestiges of postsynaptic elements remain adherent to these boutons. Numerous phagocytic astrocytes are observed throughout the lesioned area. These morphologic studies provide (direct) evidence that in situ injection of kainic acid in brain causes a selective degeneration of neurons with cell bodies in the area of the injection but spares axons that arise from perikarya outside the region but pass through or terminate in the injected area. Thus, in situ injection of kainic acid is a new technique for making selective brain lesions that will be useful for examining neuronal connectivity.
通过明视野、组织荧光和电子显微镜技术,研究了将谷氨酸的构象受限类似物海藻酸立体定向注射到大鼠纹状体后产生的形态学后遗症。对海藻酸盐注射的神经病理反应分为两个不同阶段。首先,纹状体的固有神经元在注射后的头48小时内迅速退化;其特征是细胞质尼氏体物质(染色质溶解)相继丧失、胞体收缩、核染色质聚集,最终核膜破裂。注射后1至3周,第二阶段的特征是先前有神经元的灰质中星形胶质细胞显著增殖。注射海藻酸的纹状体中几个神经元缺失的区域大致呈球形,其范围与注射的海藻酸量呈非线性关系。由于固有神经元的死亡及其突起的丧失,注射纹状体的神经纤维网明显破坏。然而,组织荧光显微镜显示,从黑质投射的多巴胺能轴突在注射海藻酸的纹状体中不会退化;电子显微镜研究表明,穿过纹状体的皮质离心纤维也不受海藻酸影响。许多突触前终扣,可能是外源性的,在注射后长达十天仍然完好;突触后成分的嗜锇遗迹仍附着在这些终扣上。在整个损伤区域观察到大量吞噬性星形胶质细胞。这些形态学研究提供了(直接)证据,即脑内原位注射海藻酸会导致注射区域内细胞体所在神经元的选择性退化,但不会损伤起源于该区域外但穿过或终止于注射区域的轴突。因此,原位注射海藻酸是一种制造选择性脑损伤的新技术,将有助于研究神经元连接性。