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(-)依托必利和7-羟基-DPAT对小鼠悬尾实验的影响。

Effects of (-)eticlopride and 7-OH-DPAT on the tail-suspension test in mice.

作者信息

Ferrari F, Giuliani D

机构信息

Department of Biomedical Sciences, University of Modena, Italy.

出版信息

J Psychopharmacol. 1997;11(4):339-44. doi: 10.1177/026988119701100409.

Abstract

The dopamine (DA) D2/D3 antagonist (-)eticlopride (0.02, 0.05 and 0.1 mg/kg), dose-dependently increased immobility in the mouse tail-suspension test. Chronic treatment with the same compound (0.05, 0.1 mg/kg, x 14 days) produced a different effect, decreasing immobility when animals were tested 24 h after the last injection. The DA D3 agonist, 7-OH-DPAT, acutely administered before the same test, behaved biphasically, increasing and decreasing mice immobility at low (0.05 and 0.1 mg/kg) and high (1 and 2 mg/kg) doses, respectively. Chronically administered 7-OH-DPAT reduced the immobility time at 2 mg/kg but not at 0.1 mg/kg. These effects, coupled with measurements of locomotor activity and evaluation of mice behaviour in different conditions, are discussed in the light of putative DA involvement in depressive states and are considered as predicting antidepressant potential.

摘要

多巴胺(DA)D2/D3拮抗剂(-)依托必利(0.02、0.05和0.1毫克/千克)在小鼠悬尾试验中剂量依赖性地增加不动时间。用相同化合物(0.05、0.1毫克/千克,连续14天)进行慢性治疗产生了不同的效果,在最后一次注射后24小时对动物进行测试时,不动时间减少。DA D3激动剂7-羟基-DPAT在相同试验前急性给药,表现为双相性,在低剂量(0.05和0.1毫克/千克)和高剂量(1和2毫克/千克)时分别增加和减少小鼠的不动时间。长期给予7-羟基-DPAT可使2毫克/千克剂量时的不动时间减少,但0.1毫克/千克剂量时则无此效果。根据多巴胺在抑郁状态中的假定作用,对这些效应以及运动活动的测量和不同条件下小鼠行为的评估进行了讨论,并被视为预测抗抑郁潜力。

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