Hui S C, Qiu B S
School of Professional and Continuing Education, University of Hong Kong, Hong Kong.
Experientia. 1996 Jan 16;52(1):66-9. doi: 10.1007/BF01922418.
Prazosin was injected i.v. at a dose of 50 micrograms/kg every 2 h for 8 h in conscious rats. Its hypotensive action significantly declined. A similar effect was also observed in rabbits pretreated with prazosin (40 micrograms/kg, i.v.) every 1 h for 4 h. In prazosin-treated rabbits, the total peripheral resistance became less responsive to phentolamine stimulation. Repeated prazosin administration abolished its ability to block receptors in a model of anococcygue muscle contraction after noradrenaline (NA) stimulation. The alpha-adrenoceptors in anococcygue muscle exhibited lower pD2 to NA and lower pA2 to prazosin in prazosin-treated rats. The results demonstrate that repeated prazosin administration reduces the effectiveness of alpha-adrenoceptors blockers.
在清醒大鼠中,以50微克/千克的剂量静脉注射哌唑嗪,每2小时注射一次,共注射8小时。其降压作用显著下降。在每1小时静脉注射哌唑嗪(40微克/千克),共注射4小时的家兔中也观察到类似效果。在经哌唑嗪处理的家兔中,总外周阻力对酚妥拉明刺激的反应性降低。重复给予哌唑嗪后,在去甲肾上腺素(NA)刺激后的肛门尾骨肌收缩模型中,其阻断受体的能力消失。在经哌唑嗪处理的大鼠中,肛门尾骨肌中的α-肾上腺素受体对NA的pD2值较低,对哌唑嗪的pA2值较低。结果表明,重复给予哌唑嗪会降低α-肾上腺素受体阻滞剂的有效性。