刺激和阻断d(2)受体对去卵巢雌性大鼠抑郁样行为的影响。

ISRN Pharmacology Pub Date : 2012-01-01 Epub Date: 2012-03-01 DOI:10.5402/2012/305645
Julia Fedotova
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引用次数: 7

摘要

本研究旨在探讨D(2)受体激动剂、喹匹罗和D(2)受体拮抗剂以及舒匹利单独或联合低剂量17β-E(2)-雌二醇(17β-E(2))对成年去卵巢雌性大鼠(OVX)的享乐效应。所有实验均采用Wistar株OVX大鼠。术后2周,大鼠在强迫游泳试验前连续14天长期服用载药、低剂量17β-E(2) (5.0 μg/大鼠)、喹匹罗(0.1 mg/kg)、舒必利(10.0 mg/kg)、喹匹罗加17β-E(2)或舒必利加17β-E(2)。我们发现舒必利显著减少OVX雌性小鼠的不活动时间。与单用舒必利治疗的大鼠相比,低剂量的17β-E(2)联合使用舒必利可显著减少OVX大鼠的不动时间。相反,喹匹罗未能改变OVX大鼠的抑郁样行为。此外,喹匹罗明显阻断了OVX大鼠17β-E(2)的抗抑郁样作用。因此,D(2)受体拮抗剂舒匹利单独或联合低剂量的17β-E(2)对OVX雌性大鼠产生抗抑郁样作用,而D(2)受体激动剂喹匹罗对OVX大鼠产生抗抑郁样作用。
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Effects of stimulation and blockade of d(2) receptor on depression-like behavior in ovariectomized female rats.

The aim of the present study was to explore the hedonic effects of D(2) receptor agonist, quinpirole and D(2) receptor antagonist, and sulpiride alone or in combination with a low dose of 17β-E(2)-estradiol (17β-E(2)) in the adult ovariectomized female rats (OVX). OVX rats of Wistar strain were used in all experiments. Two weeks after surgery rats were chronically treated with vehicle, a low dose of 17β-E(2) (5.0 μg/rat), quinpirole (0.1 mg/kg), sulpiride (10.0 mg/kg), quinpirole plus 17β-E(2), or sulpiride plus 17β-E(2) for 14 days before the forced swimming test. We found that sulpiride significantly decreased immobility time in the OVX females. A combination of sulpiride with a low dose of 17β-E(2) induced more profound decrease of immobility time in the OVX rats compared to the rats treated with sulpiride alone. On the contrary, quinpirole failed to modify depression-like behavior in the OVX rats. In addition, quinpirole significantly blocked the antidepressant-like effect of 17β-E(2) in OVX rats. Thus, the D(2) receptor antagonist sulpiride alone or in combination with a low dose of 17β-E(2) exerted antidepressant-like effect in OVX female rats, while the D(2) receptor agonist quinpirole produced depressant-like profile on OVX rats.

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