Yau Joyce L W, Wheelan Nicola, Noble June, Walker Brian R, Webster Scott P, Kenyon Christopher J, Ludwig Mike, Seckl Jonathan R
Centre for Cognitive Aging and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK; Endocrinology Unit, British Heart Foundation Centre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Centre for Cognitive Aging and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK; Endocrinology Unit, British Heart Foundation Centre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Neurobiol Aging. 2015 Jan;36(1):334-43. doi: 10.1016/j.neurobiolaging.2014.07.007. Epub 2014 Jul 15.
11Beta-hydroxysteroid dehydrogenase type 1 (11β-HSD1) locally amplifies active glucocorticoids within specific tissues including in brain. In the hippocampus, 11β-HSD1 messenger RNA increases with aging. Here, we report significantly greater increases in intrahippocampal corticosterone (CORT) levels in aged wild-type (WT) mice during the acquisition and retrieval trials in a Y-maze than age-matched 11β-HSD1(-/-) mice, corresponding to impaired and intact spatial memory, respectively. Acute stress applied to young WT mice led to increases in intrahippocampal CORT levels similar to the effects of aging and impaired retrieval of spatial memory. 11β-HSD1(-/-) mice resisted the stress-induced memory impairment. Pharmacologic inhibition of 11β-HSD1 abolished increases in intrahippocampal CORT levels during the Y-maze trials and prevented spatial memory impairments in aged WT mice. These data provide the first in vivo evidence that dynamic increases in hippocampal 11β-HSD1 regenerated CORT levels during learning and retrieval play a key role in age- and stress-associated impairments of spatial memory.
11β-羟基类固醇脱氢酶1型(11β-HSD1)在包括大脑在内的特定组织中局部放大活性糖皮质激素。在海马体中,11β-HSD1信使核糖核酸随衰老而增加。在此,我们报告,在Y迷宫的获取和检索试验中,老年野生型(WT)小鼠海马体内皮质酮(CORT)水平的增加显著高于年龄匹配的11β-HSD1基因敲除(-/-)小鼠,分别对应空间记忆受损和完好。对年轻WT小鼠施加急性应激会导致海马体内CORT水平升高,类似于衰老的影响,并损害空间记忆的检索。11β-HSD1基因敲除小鼠抵抗应激诱导的记忆损害。在Y迷宫试验期间,对11β-HSD1进行药理抑制消除了海马体内CORT水平的升高,并预防了老年WT小鼠的空间记忆损害。这些数据提供了首个体内证据,表明在学习和检索过程中海马体11β-HSD1再生的CORT水平动态增加在与年龄和应激相关的空间记忆损害中起关键作用。