Weiner N, Martin C, Wesemann W, Riederer P
J Neural Transm. 1979;46(3):253-62. doi: 10.1007/BF01250790.
Synaptosomes and synaptic membranes were isolated from rat brain after various storage times and temperatures of the tissue. Synaptosomal 5-HT uptake was diminished by about 20% within the first hour after decapitation. No significant change in the incorporation rate was observed for the seven proceeding hours if the brains were stored at room temperature. After an initial decrease of about 15%, 5-HT incorporation remained constant for at least 24 hours if the tissue was stored at 4 degrees C. Electron micrographs showed that nerve endings were highly disrupted by freezing and thawing of the brains.--The capacity of high affinity 5-HT binding to the microsomal synaptic membrane fraction decreased with the first hour by about 13% to 120--130 fmoles 5-HT/mg protein and remained almost constant for the next eight hours. Freezing at --80 degrees C of whole brain or of isolated membranes did not affect 5-HT receptor interaction.--The capacity of specific 5-HT binding to membranes isolated from human post-mortem brain was comparable to that found with synaptic membranes from rat brain. In contrast to the control values, a significant decrease in 5-HT binding was observed in membrane fractions isolated from brain after cerebral insult.
在对大鼠脑组织进行不同时长和温度的保存后,分离出了突触体和突触膜。断头后第一小时内,突触体对5-羟色胺(5-HT)的摄取减少了约20%。如果将大脑在室温下保存,在接下来的七个小时内,摄取率没有显著变化。如果将组织保存在4摄氏度,5-HT摄取在最初下降约15%后,至少24小时内保持恒定。电子显微镜照片显示,大脑的冷冻和解冻会使神经末梢受到严重破坏。——高亲和力5-HT与微粒体突触膜部分的结合能力在第一小时内下降了约13%,降至120 - 130飞摩尔5-HT/毫克蛋白质,并在接下来的八个小时内几乎保持不变。全脑或分离出的膜在-80摄氏度下冷冻并不影响5-HT受体相互作用。——从人类死后大脑分离出的膜上特异性5-HT结合能力与从大鼠大脑突触膜上发现的相当。与对照值相比,在脑损伤后从大脑分离出的膜部分中,观察到5-HT结合显著减少。