Fernandez Stephanie M, Lewis Michael C, Pechenino Angela S, Harburger Lauren L, Orr Patrick T, Gresack Jodi E, Schafe Glenn E, Frick Karyn M
Department of Psychology and Interdepartmental Neuroscience Program, Yale University, New Haven, Connecticut 06520, USA.
J Neurosci. 2008 Aug 27;28(35):8660-7. doi: 10.1523/JNEUROSCI.1968-08.2008.
The extracellular signal-regulated kinase (ERK) pathway is critical for various forms of learning and memory, and is activated by the potent estrogen 17beta-estradiol (E(2)). Here, we asked whether E(2) modulates memory via ERK activation and putative membrane-bound estrogen receptors (ERs). Using ovariectomized mice, we first demonstrate that intraperitoneal injection of 0.2 mg/kg E(2) significantly increases dorsal hippocampal levels of phosphorylated ERK protein 1 h after injection. Second, we show that E(2) administered intraperitoneally (0.2 mg/kg) or via intrahippocampal infusion (5.0 microg/side) immediately after training in an object recognition task significantly enhances memory retention, and that the beneficial effect of intraperitoneal E(2) is blocked by dorsal hippocampal inhibition of ERK activation. Third, using bovine serum albumin-conjugated 17beta-estradiol (BSA-E(2)), we demonstrate that E(2) binding at membrane-bound ERs can increase dorsal hippocampal ERK activation and enhance object memory consolidation in an ERK-dependent manner. Fourth, we show that this effect is independent of nuclear ERs, but is dependent on the dorsal hippocampus. By demonstrating that E(2) enhances memory consolidation via dorsal hippocampal ERK activation, this study is the first to identify a specific molecular pathway by which E(2) modulates memory and to demonstrate a novel role for membrane-bound ERs in mediating E(2)-induced improvements in hippocampal memory consolidation.
细胞外信号调节激酶(ERK)通路对各种形式的学习和记忆至关重要,并且可被强效雌激素17β-雌二醇(E₂)激活。在此,我们探究E₂是否通过ERK激活和假定的膜结合雌激素受体(ERs)来调节记忆。利用去卵巢小鼠,我们首先证明腹腔注射0.2mg/kg E₂在注射后1小时可显著提高背侧海马中磷酸化ERK蛋白的水平。其次,我们表明在物体识别任务训练后立即腹腔注射(0.2mg/kg)或通过海马内注射(5.0μg/侧)给予E₂可显著增强记忆保持,并且腹腔注射E₂的有益作用可被背侧海马ERK激活的抑制所阻断。第三,使用牛血清白蛋白偶联的17β-雌二醇(BSA-E₂),我们证明膜结合ERs处的E₂结合可增加背侧海马ERK激活并以ERK依赖的方式增强物体记忆巩固。第四,我们表明这种效应独立于核ERs,但依赖于背侧海马。通过证明E₂通过背侧海马ERK激活增强记忆巩固,本研究首次确定了E₂调节记忆的特定分子途径,并证明了膜结合ERs在介导E₂诱导的海马记忆巩固改善中的新作用。