卡马西平的抗抑郁作用——多巴胺能和去甲肾上腺素能药物的作用。

A Słuzewska, A Chodera
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引用次数: 0

摘要

卡马西平(CBZ) 20 mg/kg/d治疗14天,可减少大鼠行为“绝望”试验中的静止时间。两种多巴胺能受体阻滞剂:氟哌啶醇(0.5 mg/kg)和舒必利(100 mg/kg)拮抗CBZ引起的不动减少。CBZ的抗静止作用也被突触前α - 2肾上腺素受体激动剂可乐定(0.1 mg/kg)和β -肾上腺素溶药心得安(5 mg/kg)所抵消。
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Antidepressant effect of carbamazepine--the role of dopaminergic and noradrenergic agents.

Fourteen days of treatment with 20 mg/kg/day carbamazepine (CBZ) reduced the immobility time in the behavioral "despair" test in rats. Two blockers of dopaminergic receptors: haloperidol (0.5 mg/kg) and sulpiride (100 mg/kg) antagonized the reduction of immobility caused by CBZ. The anti-immobility effect of CBZ was also counteracted by clonidine (0.1 mg/kg) an agonist of presynaptic alpha 2 adrenoreceptors and propranolol (5 mg/kg) beta-adrenolytic drug.

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