Nishimura M, Komatsu R, Taquahashi Y, Shimizu Y, Satoh E
Department of Pharmacology, University of Obihiro School of Veterinary Medicine, Japan.
J Peripher Nerv Syst. 1998;3(2):111-5.
The present experiments examined the effects of phenothiazine derivatives, such as trifluoperazine and promethazine, on the release of transmitter quanta in preparations of the mouse diaphragm. The frequency (F, s-1) of miniature end-plate potentials and the quantal content (m) of endplate potentials were measured intracellularly at the same endplate in a bathing solution that contained 0.5-0.8 mM Ca2+ ions and 5 mM Mg2+ ions. Trifluoperazine (4 microM) significantly reduced both F and m. The inhibitory effect on m, but not on F, was subject to competition by Ca2+ ions. Promethazine at 48 microM, but not at 16 microM, reduced the quantal release. It was apparent that the effect of trifluoperazine was competitively antagonized by Ca2+ ions at motor nerve terminals.
本实验研究了吩噻嗪衍生物,如三氟拉嗪和异丙嗪,对小鼠膈肌标本中递质量子释放的影响。在含有0.5 - 0.8 mM钙离子和5 mM镁离子的浴液中,于同一终板处细胞内测量微小终板电位的频率(F,s⁻¹)和终板电位的量子含量(m)。三氟拉嗪(4 μM)显著降低了F和m。对m而非F的抑制作用受到钙离子的竞争性影响。48 μM的异丙嗪可降低量子释放,而16 μM则无此作用。显然,在运动神经末梢,三氟拉嗪的作用受到钙离子的竞争性拮抗。