Departamento de Fisiología (Fisiología Animal II), Facultad de Biología, Universidad Complutense, Madrid, Spain.
J Neuroendocrinol. 2011 Apr;23(4):329-44. doi: 10.1111/j.1365-2826.2011.02109.x.
We have analysed the long-term psychoneuroendocrine effects of maternal deprivation (MD) [24 h at postnatal day (PND) 9] and/or exposure to chronic unpredictable stress (CUS) during the periadolescent period (PND 28 to PND 43) in male and female Wistar rats. Animals were tested in the elevated plus maze (EPM, anxiety) at PND 44 and in two memory tests, spontaneous alternation and novel object recognition (NOT) in adulthood. The expression of hippocampal glucocorticoid (GR) and mineralocorticoid (MR) receptors, as well as of synaptophysin, neural cell adhesion molecule and brain-derived neurotrophic factor, was analysed by in situ hybridisation in selected hippocampal regions. Endocrine determinations of leptin, testosterone and oestradiol plasma levels were carried out by radioimmunoassay. Young CUS animals showed decreased anxiety behaviour in the EPM (increased percentage of time and entries in the open arms) irrespective of neonatal treatment. Memory impairments were induced by the two stressful treatments as was revealed by the NOT, with males being most clearly affected. Although each stressful procedure, when considered separately, induced different (always decrements) effects on the three synaptic molecules analysed and affected males and females differently, the combination of MD and CUS induced an unique disruptive effect on the three synaptic plasticity players. MD induced a long-term significant decrease in hippocampal GR only in males, whereas CUS tended to increase MR in males and decrease MR in females. Both neonatal MD and periadolescent CUS induced marked reductions in testosterone and oestradiol in males, whereas MD male animals also showed significantly decreased leptin levels. By contrast, in females, none of the hormones analysed was altered by any of the stressful procedures. Taking our data together in support of the 'two-hit' hypothesis, MD during neonatal life and/or exposure to CUS during the periadolescent period induced a permanent deficit in memory, which was accompanied by a decrement in markers for hippocampal plasticity. The long-term effects on body weight and hormone levels, particularly among males, might reflect sex-dependent lasting metabolic alterations as well as an impaired reproductive function.
我们分析了母源剥夺(MD)[产后第 9 天 24 小时]和/或青春期期间(第 28 至 43 天)暴露于慢性不可预测应激(CUS)对雄性和雌性 Wistar 大鼠的长期神经内分泌影响。在第 44 天的高架十字迷宫(EPM,焦虑)和成年期的自发交替和新物体识别(NOT)两项记忆测试中对动物进行了测试。通过原位杂交分析了海马糖皮质激素(GR)和盐皮质激素(MR)受体以及突触小体蛋白、神经细胞黏附分子和脑源性神经营养因子的表达。通过放射免疫测定法测定了瘦素、睾酮和雌二醇血浆水平的内分泌测定值。年轻的 CUS 动物在 EPM 中表现出焦虑行为减少(在开放臂中的时间和进入次数百分比增加),而与新生处理无关。NOT 显示两种应激处理都会导致记忆损伤,雄性受影响最明显。尽管每种应激程序单独考虑时,都会对分析的三种突触分子产生不同的(总是减少)影响,并且对雄性和雌性的影响不同,但 MD 和 CUS 的组合对三种突触可塑性分子产生了独特的破坏作用。MD 仅在雄性中诱导海马 GR 的长期显著下降,而 CUS 倾向于增加雄性中的 MR 并降低雌性中的 MR。新生 MD 和青春期 CUS 都会导致雄性中的睾酮和雌二醇明显减少,而 MD 雄性动物的瘦素水平也显著降低。相比之下,在雌性中,没有任何一种应激程序改变了任何一种分析的激素。我们的数据共同支持“双打击”假说,即新生儿期的 MD 和青春期的 CUS 暴露会导致记忆永久性缺陷,同时伴随着海马可塑性标志物的减少。对体重和激素水平的长期影响,尤其是雄性,可能反映出性别依赖性的持久代谢改变以及生殖功能受损。