Yau J L, Olsson T, Morris R G, Meaney M J, Seckl J R
University of Edinburgh, Department of Medicine, Western General Hospital, U.K.
Neuroscience. 1995 Jun;66(3):571-81. doi: 10.1016/0306-4522(94)00612-9.
The emergence of cognitive deficits in a subgroup of aged rats is associated with increased hypothalamic-pituitary-adrenal axis activity, decreased hippocampal mineralocorticoid and/or glucocorticoid receptor gene expression and neuronal loss. Short-term treatment with antidepressant drugs in young rats increases hippocampal corticosteroid receptor gene expression. In this study, the effects of chronic antidepressant administration on hippocampal mineralocorticoid and glucocorticoid receptor gene expression and spatial memory in young and aged rats were investigated. Young (eight months) and old (22 +/- 1 months) Lister-hooded rats were ranked according to watermaze performance. Matched pairs of rats were treated with amitriptyline (10 mg/kg) or saline daily for nine weeks, then reassessed in the watermaze. Amitriptyline significantly improved spatial memory in the young rats (33% increase in transfer test time) and increased hippocampal mineralocorticoid, but not glucocorticoid receptor messenger RNA expression. By contrast, in aged rats, amitriptyline had no effect on spatial memory or hippocampal corticosteroid receptor gene expression, either in cognitively unimpaired or cognitively-impaired animals. In aged rats, basal plasma corticosterone levels, which were significantly higher than in young animals, correlated negatively with spatial memory, while hippocampal glucocorticoid receptor mRNA expression correlated negatively with plasma corticosterone levels and positively with spatial memory. Amitriptyline had no significant effect on basal morning plasma corticosterone levels in either young or aged rats, but significantly decreased evening corticosterone levels in aged rats. Our data support the notion that corticosterone exerts a concentration-dependent biphasic influence, via selective activation of hippocampal mineralocorticoid and glucocorticoid receptor, on spatial memory. Amitriptyline improves spatial memory in young rats and increases hippocampal mineralocorticoid receptor gene expression. The lack of amitriptyline effect on spatial memory in aged rats may reflect decreased plasticity of both the synaptic processes underlying spatial memory and the regulation of hippocampal mineralocorticoid/glucocorticoid receptor expression, with mineralocorticoid receptors fully occupied due to elevated basal plasma corticosterone levels (in part a consequence of inadequate glucocorticoid receptor function).
老年大鼠亚组中认知缺陷的出现与下丘脑 - 垂体 - 肾上腺轴活动增加、海马盐皮质激素和/或糖皮质激素受体基因表达降低以及神经元丢失有关。在幼鼠中短期给予抗抑郁药物可增加海马糖皮质激素受体基因表达。在本研究中,研究了长期给予抗抑郁药物对幼鼠和老年大鼠海马盐皮质激素和糖皮质激素受体基因表达以及空间记忆的影响。将年轻(8个月)和老年(22±1个月)的利斯特戴帽大鼠根据水迷宫表现进行排名。配对的大鼠每天接受阿米替林(10mg/kg)或生理盐水治疗9周,然后在水迷宫中重新评估。阿米替林显著改善了幼鼠的空间记忆(转移测试时间增加33%),并增加了海马盐皮质激素,但未增加糖皮质激素受体信使核糖核酸表达。相比之下,在老年大鼠中,无论认知未受损还是认知受损的动物,阿米替林对空间记忆或海马糖皮质激素受体基因表达均无影响。在老年大鼠中,基础血浆皮质酮水平显著高于幼鼠,与空间记忆呈负相关,而海马糖皮质激素受体信使核糖核酸表达与血浆皮质酮水平呈负相关,与空间记忆呈正相关。阿米替林对幼鼠或老年大鼠的基础早晨血浆皮质酮水平均无显著影响,但显著降低了老年大鼠的夜间皮质酮水平。我们的数据支持这样的观点,即皮质酮通过选择性激活海马盐皮质激素和糖皮质激素受体,对空间记忆发挥浓度依赖性的双相影响。阿米替林改善幼鼠的空间记忆并增加海马盐皮质激素受体基因表达。阿米替林对老年大鼠空间记忆缺乏影响可能反映了空间记忆潜在的突触过程以及海马盐皮质激素/糖皮质激素受体表达调节的可塑性降低,由于基础血浆皮质酮水平升高(部分是糖皮质激素受体功能不足的结果),盐皮质激素受体已被完全占据。