Molgó J, Lemeignan M, Uchiyama T, Lechat P
Eur J Pharmacol. 1979 Jul 15;57(1):93-7. doi: 10.1016/0014-2999(79)90107-9.
The effect of kanamycin (Kn) on evoked transmitter release was examined in frog end-plates in vitro. By a presynaptic action, Kn (0.02 to 1 mM) significantly reduced the amount of acetylcholine liberated by nerve stimulation. In addition to its presynaptic effects, Kn (0.96 mM) decreased the size of the miniature end-plate potentials possibly by acting at the postsynaptic level. 3,4-Diaminopyridine (4.5 microM) reversed the presynaptic effects of Kn but did not modify its postsynaptic action.
在体外对青蛙终板进行研究,考察了卡那霉素(Kn)对诱发递质释放的影响。通过突触前作用,Kn(0.02至1 mM)显著减少了神经刺激释放的乙酰胆碱量。除了其突触前作用外,Kn(0.96 mM)可能通过作用于突触后水平而降低了微小终板电位的幅度。3,4-二氨基吡啶(4.5 microM)可逆转Kn的突触前作用,但不改变其突触后作用。