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Early-life stress induces EAAC1 expression reduction and attention-deficit and depressive behaviors in adolescent rats

机译:早期压力诱导青少年大鼠的EAAC1表达和注意力和抑郁行为

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Neonatal maternal separation (NMS), as an early-life stress (ELS), is a risk factor to develop emotional disorders. However, the exact mechanisms remain to be defined. In the present study, we investigated the mechanisms involved in developing emotional disorders caused by NMS. First, we confirmed that NMS provoked impulsive behavior, orienting and nonselective attention-deficit, abnormal grooming, and depressive-like behaviors in adolescence. Excitatory amino acid carrier 1 (EAAC1) is an excitatory amino acid transporter expressed specifically by neurons and is the route for the neuronal uptake of glutamate/aspartate/cysteine. Compared with that in the normal control group, EAAC1 expression was remarkably reduced in the ventral hippocampus and cerebral cortex in the NMS group. Additionally, EAAC1 expression was reduced in parvalbumin-positive hippocampal GABAergic neurons in the NMS group. We also found that EAAC1-knockout (EAAC1?/?) mice exhibited impulsive-like, nonselective attention-deficit, and depressive-like behaviors compared with WT mice in adolescence, characteristics similar to those of the NMS behavior phenotype. Taken together, our results revealed that ELS induced a reduction in EAAC1 expression, suggesting that reduced EAAC1 expression is involved in the pathophysiology of attention-deficit and depressive behaviors in adolescence caused by NMS.
机译:新生儿孕产妇分离(NMS),作为早期胁迫(ELS),是发展情绪障碍的危险因素。但是,确切的机制仍有待定义。在本研究中,我们调查了涉及发展NMS引起的情绪障碍的机制。首先,我们证实,NMS激发了青春期的冲动行为,定向和非选择性关注,异常的美容和抑郁的行为。兴奋性氨基酸载体1(EAAC1)是由神经元特异性表达的兴奋性氨基酸转运蛋白,并且是谷氨酸/天冬氨酸/半胱氨酸的神经元摄取的途径。与正常对照组相比,NMS组中的腹侧海马和脑皮层显着降低了EAAC1表达。另外,在NMS组中,在Parvalbumin-阳性海马甘草中的神经元中降低了EAAC1表达。我们还发现EAAC1-NOCKOUT(EAAC1?/α)小鼠表现出脉冲样式,非选择性的注意力和抑郁症状的行为,与青春期的WT小鼠相比,与NMS行为表型类似的特征相比。我们的结果表明,ELS诱导了EAAC1表达的减少,表明EAAC1表达减少涉及由NMS引起的青春期注意力和抑郁行为的病理生理学。

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