González-Aguilar F, Rodríguez J A, Alzola R H, Lupidio M C
Institut fuer Anatomie, Ruhr Universitaet am Bochum, F.R.G.
Neuroscience. 1988 Jan;24(1):9-17. doi: 10.1016/0306-4522(88)90306-5.
Brief vascular perfusion of the rat brain with a mixture of concentrated aldehydes completely insolubilized the brain protein in less than 30 s and yielded excellent ultrastructural preservation. Abundant synaptic vesicles closely and specifically attached to the presynaptic membrane were constantly detected. These vesicles appeared to undergo progressive transformation into amorphous, electron-dense material. No evidence of vesicle exocytosis was detected in the brains perfused in vivo but fixations performed 1 h after death showed abundant exocytotic-like images. The results suggest that the vesicles may not be exocytotically released to the intersynaptic cleft but disintegrate intracytoplasmically in the immediate vicinity of the presynaptic membrane.
用浓缩醛混合物对大鼠脑进行短暂血管灌注,不到30秒就能使脑蛋白完全不溶解,并能实现出色的超微结构保存。不断检测到大量紧密且特异性附着于突触前膜的突触小泡。这些小泡似乎逐渐转变为无定形的电子致密物质。在体内灌注的大脑中未检测到小泡胞吐的证据,但在死亡1小时后进行固定显示出大量类似胞吐的图像。结果表明,小泡可能不会通过胞吐作用释放到突触间隙,而是在突触前膜紧邻区域的细胞质内解体。