O'Leary M E, Suszkiw J B
J Neurochem. 1983 Apr;40(4):1192-5. doi: 10.1111/j.1471-4159.1983.tb08115.x.
The effects of 1 and 10 mM colchicine on the K+-evoked release of preformed and newly synthesized acetylcholine and on the K+-depolarization-stimulated uptake of 45Ca were compared in rat brain synaptosomes. Preincubation of synaptosomes with 1 mM colchicine had little effect on transmitter release and on uptake of 45Ca; 10 mM colchicine inhibited both the release of transmitter and uptake of 45Ca by 58%. Since 1 mM colchicine has been shown to disaggregate intrasynaptosomal microtubules almost completely, but to be without effect on release of either preformed or newly synthesized acetylcholine in our experiments, it is concluded that colchicine modifies transmitter release by reducing Ca2+ influx, rather than by its postulated intracellular action on microtubule-mediated transmitter mobilization. In addition, 1 and 10 mM cholchicine significantly inhibited the high-affinity choline uptake in synaptosomes. This hemicholinium-like action of colchicine may contribute to the reduction of transmitter release.
在大鼠脑突触体中比较了1 mM和10 mM秋水仙碱对预先形成的和新合成的乙酰胆碱的钾离子诱发释放以及对钾离子去极化刺激的45Ca摄取的影响。突触体与1 mM秋水仙碱预孵育对递质释放和45Ca摄取几乎没有影响;10 mM秋水仙碱使递质释放和45Ca摄取均抑制58%。由于在我们的实验中已表明1 mM秋水仙碱几乎能完全拆散突触体内的微管,但对预先形成的或新合成的乙酰胆碱的释放均无影响,因此得出结论:秋水仙碱通过减少Ca2+内流而非通过其假定的对微管介导的递质动员的细胞内作用来改变递质释放。此外,1 mM和10 mM秋水仙碱显著抑制突触体中的高亲和力胆碱摄取。秋水仙碱的这种类半胱氨酸样作用可能有助于减少递质释放。