Kanamaru M, Iwase M, Homma I
Department of Physiology, Showa University School of Medicine, Tokyo, Japan.
Neurosci Lett. 1994 Mar 14;169(1-2):35-8. doi: 10.1016/0304-3940(94)90350-6.
Administration of 1.5, 5.0 and 15 nmol histamine (HA) into the fourth ventricle (IVth) decreased tracheal pressure (PT) dose-dependently in anesthetized rabbits. Maximum decrease of PT occurred 0.9 +/- 0.1 min (mean +/- S.E.M., n = 9) after administration of 15 nmol, and recovery occurred at 4.5 +/- 1.0 min (n = 9). The decrease of PT was blocked by the H1 receptor antagonist, pyrilamine administration into the IVth, or intravenous injection of the alpha-adrenoceptor antagonist, phentolamine. Recovery from the PT decrease was delayed by the H2 receptor antagonist, cimetidine. The results suggest that HA centrally decreases PT through H1 receptors, which action is mediated by the sympathetic nervous system, and this decrease may be modulated through H2 receptors.
向麻醉兔的第四脑室注射1.5、5.0和15纳摩尔组胺(HA)可使气管压力(PT)呈剂量依赖性降低。注射15纳摩尔后,PT在0.9±0.1分钟(平均值±标准误,n = 9)时出现最大降幅,4.5±1.0分钟(n = 9)时恢复。第四脑室内注射H1受体拮抗剂吡苄明或静脉注射α-肾上腺素能受体拮抗剂酚妥拉明可阻断PT的降低。H2受体拮抗剂西咪替丁可延迟PT降低后的恢复。结果表明,HA通过H1受体在中枢降低PT,该作用由交感神经系统介导,且这种降低可能通过H2受体进行调节。