Keenan P A, Ezzat W H, Ginsburg K, Moore G J
Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, UHC-4J, 4201 St. Antoine, Detroit, MI 48201, USA.
Psychoneuroendocrinology. 2001 Aug;26(6):577-90. doi: 10.1016/s0306-4530(01)00013-0.
The hippocampus has long been presumed the primary site of action of estrogens on cognition; and explicit memory is considered the cognitive function most vulnerable to menopausal loss of estrogen. We hypothesize instead that the prefrontal cortex and its neural circuitry are prime mediators of estrogen's role in cognition. We also propose that previously reported menopausal cognitive decline, presumed to be hippocampally mediated, may be secondary to executive dysfunction. We used a cross sectional design to compare the performance of nine menopausal women on hormone replacement therapy (HRT) and 10 menopausal women with no prior exposure to HRT on a battery of neuropsychological tests. The battery was comprised primarily of tests of memory and executive functioning. Executive functioning is mediated by the frontal lobes and encompasses working memory, directed attention, the inhibition of inappropriate responses, cognitive set switching, and behavioral monitoring. Unlike most previous studies, we used a memory measure that yields multiple scores reflecting various problem-solving strategies and error types, thus isolating spared and impaired cognitive processes. Results yielded both qualitative and quantitative evidence for disruption of cognitive processes subserved by the frontal lobes rather than the hippocampus: 1) despite intact free recall on a list-learning task (CVLT), untreated menopausal women were relatively impaired in correctly recognizing words previously learned and distinguishing them from items not on the list (discriminability), 2) untreated women also had difficulty inhibiting inappropriate responses in the form of perseverative errors, and 3) the non-HRT group consistently performed worse on the N-back test of working memory. The prefrontal cortex is critical for intact working memory and estrogen enhances performance on working memory tasks. In conclusion, this study provides preliminary evidence for executive dysfunction in untreated menopausal women as women with HRT outperformed women without HRT on tests requiring directed attention, inhibition of inappropriate responses, and cognitive set switching.
长期以来,海马体一直被认为是雌激素作用于认知的主要部位;而外显记忆被视为最易受绝经后雌激素丧失影响的认知功能。相反,我们假设前额叶皮质及其神经回路是雌激素在认知中发挥作用的主要调节因子。我们还提出,先前报道的被认为由海马体介导的绝经后认知衰退,可能继发于执行功能障碍。我们采用横断面设计,比较了9名接受激素替代疗法(HRT)的绝经后女性和10名未接受过HRT的绝经后女性在一系列神经心理学测试中的表现。该测试主要包括记忆和执行功能测试。执行功能由额叶介导,包括工作记忆、定向注意力、抑制不适当反应、认知定势转换和行为监测。与以往大多数研究不同,我们使用了一种记忆测量方法,该方法产生多个分数,反映各种解决问题的策略和错误类型,从而分离出未受损和受损的认知过程。结果产生了定性和定量证据,表明额叶而非海马体所支持的认知过程受到破坏:1)尽管在列表学习任务(CVLT)上自由回忆完好,但未接受治疗的绝经后女性在正确识别先前学过的单词并将其与不在列表中的项目区分开来(辨别力)方面相对受损,2)未接受治疗的女性在抑制以持续性错误形式出现的不适当反应方面也有困难,3)非HRT组在工作记忆的N-back测试中始终表现较差。前额叶皮质对完整的工作记忆至关重要,雌激素可提高工作记忆任务的表现。总之,本研究为未接受治疗的绝经后女性存在执行功能障碍提供了初步证据,因为接受HRT的女性在需要定向注意力、抑制不适当反应和认知定势转换的测试中表现优于未接受HRT的女性。