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雌二醇和氟哌啶醇对猴实验性迟发性运动障碍的相似作用。

Similar effect of estradiol and haloperidol on experimental tardive dyskinesia in monkeys.

作者信息

Bédard P J, Boucher R, Daigle M, Di Paolo T

出版信息

Psychoneuroendocrinology. 1984;9(4):375-9. doi: 10.1016/0306-4530(84)90044-1.

Abstract

In a group of ovariectomized monkeys, a persistent buccolingual dyskinesia resembling tardive dyskinesia was induced by an upper midbrain lesion. This dyskinesia was increased by apomorphine. A single dose of haloperidol (1 mg/kg) reduced the effect of apomorphine after 24 hours and caused an increase in CSF homovanillic acid. Fifteen days later, however, the response to apomorphine was markedly enhanced. Estradiol benzoate (0.5 mg sc) had a similar biphasic effect, although of lesser magnitude. In a different group of lesioned but non-dyskinetic animals, the CSF concentration of HVA also was elevated 24 hours after estradiol. These results support our hypothesis that estradiol shares several properties with neuroleptics, and in particular, reduces, then enhances the sensitivity of striatal dopaminergic receptors.

摘要

在一组卵巢切除的猴子中,上中脑损伤诱发了一种类似于迟发性运动障碍的持续性颊舌运动障碍。阿扑吗啡可加重这种运动障碍。单次给予氟哌啶醇(1毫克/千克)在24小时后可降低阿扑吗啡的作用,并导致脑脊液中高香草酸增加。然而,15天后,对阿扑吗啡的反应明显增强。苯甲酸雌二醇(0.5毫克皮下注射)也有类似的双相作用,尽管程度较轻。在另一组有损伤但无运动障碍的动物中,雌二醇给药24小时后,脑脊液中HVA浓度也升高。这些结果支持我们的假设,即雌二醇与抗精神病药物有若干共同特性,尤其是先降低然后增强纹状体多巴胺能受体的敏感性。

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