Reaven G M, Dall'Aglio E
J Cardiovasc Pharmacol. 1982;4 Suppl 2:S248-50.
Prazosin was administered by intraperitoneal injection (0.3 or 3.0 mg/kg) to normal chow-fed male rats for 14 days. Mean +/- SEM plasma triglyceride levels were lower (p less than 0.001) in the prazosin-treated rats (74 +/- 12 mg/dl and 72 +/- 9 mg/dl) than in saline-injected control rats (115 +/- 11 mg/dl). This effect was associated with commensurate reductions in very low density lipoprotein-triglyceride secretion in prazosin-treated rats. No changes were noted in either plasma total or high density lipoprotein cholesterol concentrations. In addition, prazosin was capable of reducing by approximately 50% the elevation in plasma triglyceride concentration produced by a high glucose diet in control rats. The mechanism of the observed effect of prazosin on very low density lipoprotein metabolism in the rat remains to be defined.
将哌唑嗪(0.3或3.0毫克/千克)腹腔注射给正常喂食普通饲料的雄性大鼠,持续14天。与注射生理盐水的对照大鼠(115±11毫克/分升)相比,接受哌唑嗪治疗的大鼠(74±12毫克/分升和72±9毫克/分升)的平均±标准误血浆甘油三酯水平较低(p<0.001)。这种作用与哌唑嗪治疗的大鼠极低密度脂蛋白 - 甘油三酯分泌相应减少有关。血浆总胆固醇或高密度脂蛋白胆固醇浓度均未观察到变化。此外,哌唑嗪能够将高糖饮食导致的对照大鼠血浆甘油三酯浓度升高降低约50%。哌唑嗪对大鼠极低密度脂蛋白代谢的观察作用机制尚待确定。