Brain Sciences Institute, Swinburne University of Technology, Hawthorn, VIC, Australia.
J Psychopharmacol. 2011 Dec;25(12):1614-22. doi: 10.1177/0269881110370506. Epub 2010 Jun 18.
Estrogen may be involved in schizophrenia by inhibiting serotonin-1A (5-HT(1A)) receptor function. We examined the effects of estrogen pre-treatment on modulation of loudness dependence of the auditory evoked potential (LDAEP) and mismatch negativity by the 5-HT(1A) receptor partial agonist, buspirone. Using a double-blind, placebo-controlled, repeated-measures design in healthy female volunteers, we observed that buspirone treatment significantly increased LDAEP slope. Estrogen increased LDAEP slope on its own, and a further LDAEP increase by buspirone was not seen after estrogen pre-treatment. Similar results were observed for mismatch negativity, where buspirone caused a small increase of latency, although not amplitude, after placebo but not estrogen pre-treatment, which enhanced mismatch negativity latency on its own. These results are in line with our previous findings on prepulse inhibition showing an inhibitory effect of estrogen on the action of buspirone. Taken together, these data suggest that estrogen may inhibit 5-HT(1A) receptor-mediated disruptions of auditory processing.
雌激素可能通过抑制 5-羟色胺 1A(5-HT1A)受体功能而参与精神分裂症。我们研究了雌激素预处理对 5-HT1A 受体部分激动剂丁螺环酮调制听觉诱发电位(LDAEP)和失匹配负波的影响。在健康女性志愿者中采用双盲、安慰剂对照、重复测量设计,我们观察到丁螺环酮治疗显著增加了 LDAEP 斜率。雌激素本身增加了 LDAEP 斜率,而雌激素预处理后,丁螺环酮不再引起 LDAEP 的进一步增加。失匹配负波也观察到类似的结果,丁螺环酮引起潜伏期的小增加,尽管在安慰剂但不是雌激素预处理后,振幅没有变化,而雌激素本身增强了失匹配负波的潜伏期。这些结果与我们之前关于前脉冲抑制的研究结果一致,表明雌激素对丁螺环酮的作用具有抑制作用。综上所述,这些数据表明,雌激素可能抑制 5-HT1A 受体介导的听觉处理障碍。