Neurophysiology Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.
Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Dev Neurosci. 2020;42(2-4):135-144. doi: 10.1159/000512221. Epub 2020 Dec 18.
Early life stress is a well-described risk factor of anxiety disorders in adulthood. Dysfunction in GABA/glutamate receptors and their functional regulator, calcineurin, is linked to anxiety disorders. Here, we investigated the effect of early life stress, such as repeated maternal separation (MS; 3 h per day from postnatal day [P] 2 to 11), on changes in the expression of calcineurin as well as the ionotropic glutamatergic and GABAergic receptors including α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), N-methyl-D-aspartate (NMDA) and GABAA receptors in the hippocampus and prefrontal cortex (PFC) of adolescent (P35) and adult (P62) male Wistar rats and their correlations with anxiety-like behavior in adulthood.
The protein levels were assessed by Western blot analysis. Anxiety-like behavior was measured in the elevated plus maze (EPM) and open field (OF) tests.
MS induced a regional transient decrease of glutamate receptors expression at P35, with decreased NMDA and AMPA receptor levels, respectively, in the hippocampus and PFC, suggesting a possible decrease in excitatory synaptic strength. In contrast to glutamate receptors, MS had long-lasting influence on GABAA receptor and calcineurin levels, with reduced expression of GABAA receptor and calcineurin in both brain regions at P35 that continued into adulthood. These results were accompanied by increased anxiety behavior in adulthood, shown by lower percentage of number of total entries and time spent in the open arms of the EPM, and by lower time spent and number of entries in the OF central area.
Together, our study suggests that GABAA receptors via calcineurin-dependent signaling pathways may play an important role in the expression of stress-induced anxiety-like behavior.
早期生活压力是成年期焦虑障碍的一个众所周知的风险因素。GABA/谷氨酸受体及其功能调节剂钙调神经磷酸酶的功能障碍与焦虑障碍有关。在这里,我们研究了早期生活压力(如重复的母体分离(MS);从出生后第 2 天到第 11 天每天 3 小时)对钙调神经磷酸酶表达变化的影响,以及离子型谷氨酸能和 GABA 能受体,包括α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)、N-甲基-D-天冬氨酸(NMDA)和 GABA A 受体在青春期(P35)和成年期(P62)雄性 Wistar 大鼠海马和前额叶皮层(PFC)中的表达变化,及其与成年期焦虑样行为的相关性。
通过 Western blot 分析评估蛋白水平。使用高架十字迷宫(EPM)和旷场(OF)测试测量焦虑样行为。
MS 诱导 P35 时谷氨酸受体表达的区域性短暂下降,分别导致海马体和 PFC 中 NMDA 和 AMPA 受体水平降低,提示兴奋性突触强度可能降低。与谷氨酸受体相反,MS 对 GABA A 受体和钙调神经磷酸酶水平的影响持续时间较长,P35 时两个脑区的 GABA A 受体和钙调神经磷酸酶表达降低,并持续到成年期。这些结果伴随着成年期焦虑行为的增加,表现在 EPM 中总进入次数和开放臂停留时间的百分比降低,以及 OF 中央区域停留时间和进入次数减少。
总之,我们的研究表明,GABA A 受体通过钙调神经磷酸酶依赖性信号通路可能在应激诱导的焦虑样行为表达中发挥重要作用。