Ishitani R, Iwamoto T
Jpn J Pharmacol. 1977 Dec;27(6):755-62. doi: 10.1254/jjp.27.755.
After administration of H3-imipramine, H3-dimetacrine and S35-chlorpromazine by the direct lateral intraventricular injection, synaptosomes-rich fraction (F-B) was isolated from rat cerebral cortex by differential and 3-stepwise density gradient centrifugation. The isolated F-B fraction was treated by hyposmotic-lysis followed by freezing and thawing once or 15 times and, furthermore, fractionated into the subsynaptosomal distribution of these drugs showed the same distribution patterns, i.e., the larger portion of radioactivity was recovered in the synaptic ghost membranes-rich fractions. On the other hand, synaptic vesicles-rich fractions contained less radioactivity. On the disrupting process of F-B fraction, when the F-B fraction was treated by hyposmotic-lysis followed by freezing and thawing 15 times, only pellet (FD-6) fraction was obtained as compared with freezing and thawing once (4 interphase layers were obtained). Morphological examination revealed that the synaptic ghost membranes were located in the FD-6 fraction, but morphological damages were not observed. Under these conditions, H3-imipramine showed a 74.1% of release from the synaptosomes, while release with H3-dimetacrine and S35-chlorpromazine was 3.9 and 11.3%, respectively.
通过直接侧脑室注射给予H3-丙咪嗪、H3-二甲他林和S35-氯丙嗪后,采用差速离心和三步密度梯度离心法从大鼠大脑皮层分离出富含突触体的部分(F-B)。将分离得到的F-B部分进行低渗裂解处理,然后冷冻和解冻1次或15次,此外,将这些药物的亚突触体分布进行分级分离,结果显示相同的分布模式,即大部分放射性在富含突触膜空泡的部分中回收。另一方面,富含突触小泡的部分放射性较少。在F-B部分的破坏过程中,当F-B部分经低渗裂解后冷冻和解冻15次时,与冷冻和解冻1次(获得4个中间相层)相比,仅获得沉淀(FD-6)部分。形态学检查显示突触膜空泡位于FD-6部分,但未观察到形态学损伤。在这些条件下,H3-丙咪嗪从突触体中的释放率为74.1%,而H3-二甲他林和S35-氯丙嗪的释放率分别为3.9%和11.3%。