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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Antimanic-like effect of tamoxifen is not reproduced by acute or chronic administration of medroxyprogesterone or clomiphene.
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Antimanic-like effect of tamoxifen is not reproduced by acute or chronic administration of medroxyprogesterone or clomiphene.

机译:他莫昔芬的抗躁狂样作用不能通过急性或慢性给予甲羟孕酮或克罗米芬来重现。

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摘要

Tamoxifen, a protein kinase C (PKC) inhibitor and antiestrogenic drug, has clinical antimanic effects and blocks psychostimulant-induced hyperlocomotion. Medroxyprogesterone (MPA), which has antiestrogenic effects, also exerts some clinical benefits in female manic patients and partially blocks amphetamine-induced hyperlocomotion, indicating that the antiestrogenic effect of tamoxifen could contribute to its antimanic effect. The present study evaluated the effect of acute and chronic (21 day) treatment of two antiestrogenic drugs, MPA and clomiphene (an estrogenic receptor antagonist), on methylphenidate (MPH, 5.0mg/kg)-induced hyperlocomotion in mice, an animal model of mania. Acute and chronic tamoxifen administration was used as a positive control. Acute and chronic tamoxifen (1.0mg/kg) administration blocked MPH-induced hyperlocomotion. Acute and chronic MPA (acute: 3.0 or 6.0mg/kg; chronic: 3.0mg/kg) and clomiphene (acute: 1.5 or 3.0mg/kg; chronic: 1.5mg/kg) treatment did not alter MPH-induced hyperlocomotion. These results indicate that tamoxifen exerts antimanic-like effects, and reduced estrogenic activity does not have antimanic-like effects in this psychostimulant-induced hyperlocomotion model. Therefore, the antiestrogenic effect of tamoxifen likely does not contribute to its antimanic effect, which may instead be related to its effect on PKC activity. Therefore, PKC inhibition may be associated with the antimanic effect of mood stabilizers.
机译:他莫昔芬是一种蛋白激酶C(PKC)抑制剂和抗雌激素药,具有临床抗躁狂作用,并能阻止精神刺激药引起的运动过度。具有抗雌激素作用的甲羟孕酮(MPA)在女性躁狂患者中也具有一定的临床益处,并部分阻断苯丙胺引起的运动过度,表明他莫昔芬的抗雌激素作用可能有助于其抗躁作用。本研究评估了两种抗雌激素药物MPA和克罗米芬(一种雌激素受体拮抗剂)的急性和慢性(21天)治疗对小鼠哌醋甲酯(MPH,5.0mg / kg)诱导的运动过度的影响,这是一种动物模型狂躁。急性和慢性他莫昔芬给药被用作阳性对照。急性和慢性他莫昔芬(1.0mg / kg)给药可阻断MPH引起的运动过度。急性和慢性MPA(急性:3.0或6.0mg / kg;慢性:3.0mg / kg)和克罗米芬(急性:1.5或3.0mg / kg;慢性:1.5mg / kg)治疗未改变MPH引起的运动过度。这些结果表明,他莫昔芬发挥抗躁狂样作用,而降低的雌激素活性在这种精神兴奋剂诱发的超运动模型中没有抗躁狂样作用。因此,他莫昔芬的抗雌激素作用可能不有助于其抗躁狂作用,而可能与其对PKC活性的作用有关。因此,PKC抑制可能与情绪稳定剂的抗躁狂作用有关。

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