Rankin G O, Watkins B E, Sawutz D G
Arch Int Pharmacodyn Ther. 1984 Oct;271(2):263-74.
The development of tolerance to the antihypertensive effects of guanethidine was determined in one-kidney one clip and two-kidney one clip renovascular hypertensive rats and spontaneously hypertensive rats (SHR). The effect of gender on the tolerance development was also studied in SHR. Although initial guanethidine administration acutely reduced arterial pressure in all hypertensive models, initial dose responsiveness to the blood pressure lowering effects of guanethidine (50 mg/kg, i.p.) was greatest in male SHR. After two weeks of daily guanethidine dosing (50 mg/kg/day, i.p.) only female SHR demonstrated an acute depressor response to the day 14 guanethidine dose. During the two week dosing interval tolerance development began after day 3 in all models, and systolic pressure (SP) was not significantly different from preguanethidine values in tolerant animals by day 7. In both renovascular hypertensive models a subpopulation of guanethidine responders was identified which maintained a lowered SP (p less than 0.05) after day 3. SHR demonstrated a high degree of tolerance after day 7 regardless of gender. Tolerance did not develop to the guanethidine-induced bradycardia in any model. These data suggest that both renovascular models and SHR are suitable models for studying the mechanism(s) of tolerance development to guanethidine and possibly other sympatholytic drugs.
在单肾单夹和双肾单夹肾血管性高血压大鼠以及自发性高血压大鼠(SHR)中测定了对胍乙啶降压作用耐受性的发展。还在SHR中研究了性别对耐受性发展的影响。尽管最初给予胍乙啶能在所有高血压模型中急性降低动脉血压,但胍乙啶(50mg/kg,腹腔注射)对血压降低作用的初始剂量反应性在雄性SHR中最大。在每天给予胍乙啶(50mg/kg/天,腹腔注射)两周后,只有雌性SHR对第14天的胍乙啶剂量表现出急性降压反应。在两周的给药间隔期间,所有模型在第3天后开始出现耐受性发展,到第7天时,耐受性动物的收缩压(SP)与给予胍乙啶前的值无显著差异。在两种肾血管性高血压模型中,均鉴定出一部分对胍乙啶有反应的动物,它们在第3天后SP维持在较低水平(p<0.05)。无论性别如何,SHR在第7天后均表现出高度耐受性。在任何模型中,对胍乙啶诱导的心动过缓均未产生耐受性。这些数据表明,肾血管性高血压模型和SHR都是研究对胍乙啶以及可能对其他抗交感神经药物耐受性发展机制的合适模型。