卡托普利在动物模型中缺乏类似抗抑郁药的活性。

L Baran, J Siwanowicz, G Nowak, E Przegaliński
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引用次数: 0

摘要

卡托普利是一种血管紧张素转换酶抑制剂,在几种动物模型中评估了其潜在的抗抑郁活性。3 ~ 30mg /kg剂量组既不影响利血平或阿吗啡诱导的小鼠低温,也不减少小鼠和大鼠游泳力实验中的静止时间。此外,反复给药卡托普利(10 mg/kg,每天两次,连续14天)既没有改变大鼠皮质β -肾上腺素受体的密度或亲和力,也没有改变诺非芬素诱导的运动亢进。这些结果表明卡托普利在动物模型中没有抗抑郁样活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Captopril lacks the antidepressant-like activity in animal models.

Captopril, an angiotensin converting enzyme inhibitor, was evaluated for a potential antidepressive activity in several animal models. The drug administered in doses of 3-30 mg/kg ip neither affected the reserpine- or apomorphine-induced hypothermia in mice nor reduced the immobility time in the forces swimming test in mice and rats. Moreover, captopril administered repeatedly (10 mg/kg ip, twice daily for 14 days) neither changed the density or affinity of cortical beta-adrenoceptors nor modified the nomifensine-induced locomotor hyperactivity in rats. These results suggest that captopril has no antidepressant-like activity in animal models.

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