Saito T, Tagami H, Kamei C, Tasaka K
Arch Int Pharmacodyn Ther. 1984 Sep;271(1):127-34.
Effects of pyrilamine and diphenhydramine on isolated spinal cords of bullfrogs were studied in order to clarify the mechanisms of depressant and stimulant actions of H1-blockers on the central nervous system. Pyrilamine and diphenhydramine depressed both the DR-VRP and DR-DRP. Pyrilamine and diphenhydramine also suppressed L-glutamate-induced depolarization of the motoneurones, but they did not depress GABA depolarization at the dorsal root terminals. By switching the perfusate to drug-free Ringer solution, depressed amplitudes of DR-VRP were suddenly increased over the control level (rebound phenomenon). The rebound increase of DR-VRP was inhibited by either tetrodotoxin or D-600. These results suggest that the rebound phenomenon may be due to the effect of H1-blockers 1) inhibiting transmitter release participating in presynaptic inhibition and 2) inducing a rapid recovery from the depressed influx of Na+ and Ca2+ into motoneurones.
为阐明H1受体阻滞剂对中枢神经系统的抑制和兴奋作用机制,研究了吡苄明和苯海拉明对牛蛙离体脊髓的作用。吡苄明和苯海拉明均降低了背根节-腹根逆向电位(DR-VRP)和背根节-背根逆向电位(DR-DRP)。吡苄明和苯海拉明还抑制了L-谷氨酸诱导的运动神经元去极化,但它们并未抑制背根终末的GABA去极化。通过将灌流液换成无药的林格液,DR-VRP的降低幅度突然超过对照水平增加(反弹现象)。DR-VRP的反弹增加被河豚毒素或D-600抑制。这些结果表明,反弹现象可能是由于H1受体阻滞剂的作用:1)抑制参与突触前抑制的递质释放;2)诱导运动神经元中Na+和Ca2+内流减少后的快速恢复。