Locklear M N, Bhamidipaty S, Kritzer M F
Graduate Program in Neuroscience, Stony Brook University, Stony Brook, New York 11794-5230, United States.
Department of Neurobiology and Behavior, Stony Brook University, Stony Brook, New York 11794-5230, United States.
Neuroscience. 2015 Mar 12;288:73-85. doi: 10.1016/j.neuroscience.2014.12.032. Epub 2014 Dec 27.
Gonadectomy in adult male rats significantly impairs spatial working memory, behavioral flexibility and other functions associated with the prefrontal cortex (PFC). However, the mechanisms through which this occurs are largely unknown. In this study, intracortical drug challenge with the selective N-methyl-d-aspartate receptor (NMDAR) antagonist D(-)-2-amino-5-phosphonopentanoic acid (APV) was combined with Barnes maze testing, gonadectomy (GDX) and hormone replacement (17β-estradiol, testosterone propionate) to explore the contributions of NMDAR-mediated activity within the PFC to hormone effects on spatial cognition in adult male rats. Previous studies have shown that Barnes maze testing reveals significant estrogen-dependent, GDX-induced deficits in spatial working memory and androgen-sensitive, GDX-induced deficits in spatial search strategy. Here we found that bilateral infusion of APV into the medial PFC prior to testing significantly improved both sets of behaviors in gonadectomized rats and significantly worsened performance measures in gonadally intact controls. In hormone-replaced cohorts, we further found that behaviors that are normally similar to controls were significantly disrupted by APV, and those that are normally similar to gonadectomized rats were rescued by intracortical APV infusion. There were, however, no residual effects of APV on retention testing conducted 24h later. Together these findings suggest that hormone regulation of NMDAR-mediated activity specifically within the PFC may be fundamental to the effects of gonadal steroids on spatial cognition in males. Our findings further identify NMDAR antagonists as potentially novel, non-steroidal means of attenuating the cognitive deficits that can accompany gonadal hormone decline in human males in aging, clinical cases of hypogonadalism and in certain neurologic and psychiatric illnesses. Accordingly, it may be important to obtain in males the kind of detailed knowledge concerning hormone effects on, for example, the channel and electrophysiological properties of NMDAR that currently exists for the female brain.
成年雄性大鼠的性腺切除术会显著损害空间工作记忆、行为灵活性以及与前额叶皮质(PFC)相关的其他功能。然而,其发生机制在很大程度上尚不清楚。在本研究中,将选择性N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂D-(-)-2-氨基-5-磷酸戊酸(APV)的皮质内药物激发与巴恩斯迷宫测试、性腺切除术(GDX)和激素替代(17β-雌二醇、丙酸睾酮)相结合,以探究PFC内NMDAR介导的活动对成年雄性大鼠性腺激素对空间认知影响的作用。先前的研究表明,巴恩斯迷宫测试揭示了空间工作记忆中显著的雌激素依赖性、GDX诱导的缺陷以及空间搜索策略中雄激素敏感性、GDX诱导的缺陷。在此我们发现,在测试前将APV双侧注入内侧PFC可显著改善去势大鼠的两组行为,并显著恶化性腺完整对照组的行为指标。在激素替代组中,我们进一步发现,通常与对照组相似的行为会被APV显著破坏,而通常与去势大鼠相似的行为会通过皮质内注入APV得到挽救。然而,APV对24小时后进行的记忆测试没有残留影响。这些发现共同表明,PFC内NMDAR介导的活动的激素调节可能是性腺类固醇对雄性空间认知影响的基础。我们的研究结果进一步确定NMDAR拮抗剂是一种潜在的新型非甾体手段,可减轻衰老、性腺功能减退临床病例以及某些神经和精神疾病中男性性腺激素下降可能伴随的认知缺陷。因此,对于男性而言,获取目前女性大脑中存在的关于激素对NMDAR通道和电生理特性等影响的详细知识可能很重要。