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Estrogen Prevents 5-HT1A Receptor-Induced Disruptions of Prepulse Inhibition in Healthy Women

机译:雌激素可预防健康女性的5-HT1A受体诱导的前脉冲抑制破坏。

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The sex steroid hormone, estrogen, has been proposed to be protective against schizophrenia. This study examined the effects of estrogen treatment on modulation of prepulse inhibition (PPI) by the serotonin-1A (5-HT1A) receptor partial agonist, buspirone. PPI is a model of sensorimotor gating, which is deficient in schizophrenia and other mental illnesses. A total of 11 healthy women were tested following four acute treatment conditions: placebo, buspirone (Buspar; 5mg), estradiol (Estrofem; 2mg), and combined buspirone and estradiol. Electromyogram activity was measured across three interstimulus intervals (ISI): 30, 60, and 120ms. There was no significant effect of either drug treatment on startle amplitude or habituation. At 120ms ISI, buspirone caused a significant disruption of PPI and pretreatment with estrogen prevented this disruption. Estrogen treatment, administered in the appropriate experimental conditions, prevented PPI deficits induced by 5-HT1A receptor activation and may therefore also play a protective role in sensorimotor gating deficits in schizophrenia.
机译:性类固醇激素,雌激素,已被提议对精神分裂症具有保护作用。这项研究检查了雌激素治疗对5-羟色胺-1A(5-HT1A)受体部分激动剂丁螺环酮对前脉冲抑制(PPI)的调节作用。 PPI是感觉运动门控的模型,其在精神分裂症和其他精神疾病中缺乏。在以下四种急性治疗条件下对总共11名健康妇女进行了测试:安慰剂,丁螺环酮(Buspar; 5mg),雌二醇(Estrofem; 2mg)以及丁螺环酮和雌二醇的组合。在三个刺激间隔(ISI):30、60和120毫秒内测量肌电图活性。药物治疗对惊吓幅度或适应性均无显着影响。在120ms ISI时,丁螺环酮引起PPI的显着破坏,而雌激素预处理可防止这种破坏。在适当的实验条件下进行的雌激素治疗可预防由5-HT1A受体激活引起的PPI缺乏,因此也可在精神分裂症的感觉运动门控缺乏中起保护作用。

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