Turkkan J S, Hienz R D, Allen R P, Bezold H J
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Pharmacol Biochem Behav. 1992 Jul;42(3):465-71. doi: 10.1016/0091-3057(92)90141-2.
Spontaneous motor activity of normotensive and renovascular hypertensive baboons was measured during oral dosing with the beta-adrenergic antagonists atenolol HCl (2.6 mg/kg/day) and d,l-propranolol HCl (6.8 mg/kg twice daily) in separate studies. Each study administered active drug for 21 consecutive days. Piezoelectric monitors sensitive to movement were worn continuously by the baboons. Propranolol decreased overall 24-h average activity during the third week of dosing in normotensive baboons but not in renovascular hypertensive baboons. The greatest reductions in activity averaged 20% at those times of day corresponding to the second daily drug dose both in normotensive baboons and, at this time of day only, in the majority of hypertensive baboons. Activity decreases reversed to baseline levels when propranolol was discontinued. For atenolol, most normotensive but no hypertensive baboons showed decreases in activity at the time of day corresponding to the daily drug dose.
在单独的研究中,给正常血压和肾血管性高血压狒狒口服β-肾上腺素能拮抗剂盐酸阿替洛尔(2.6毫克/千克/天)和盐酸消旋普萘洛尔(6.8毫克/千克,每日两次)时,测量了它们的自发运动活动。每项研究连续21天给予活性药物。狒狒连续佩戴对运动敏感的压电监测器。普萘洛尔降低了正常血压狒狒给药第三周的24小时总体平均活动,但对肾血管性高血压狒狒没有影响。在对应于每日第二次给药的时间段,正常血压狒狒和仅在该时间段的大多数高血压狒狒的活动平均最大降幅为20%。停用普萘洛尔后,活动减少恢复到基线水平。对于阿替洛尔,大多数正常血压狒狒在对应于每日给药的时间段活动减少,但高血压狒狒没有。