首页> 美国卫生研究院文献>Frontiers in Behavioral Neuroscience >AMPA Receptor–mTOR Activation is Required for the Antidepressant-Like Effects of Sarcosine during the Forced Swim Test in Rats: Insertion of AMPA Receptor may Play a Role
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AMPA Receptor–mTOR Activation is Required for the Antidepressant-Like Effects of Sarcosine during the Forced Swim Test in Rats: Insertion of AMPA Receptor may Play a Role

机译:在大鼠强迫游泳试验中肌氨酸的抗抑郁样作用需要AMPA受体-mTOR激活:AMPA受体的插入可能起一定作用

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摘要

Sarcosine, an endogenous amino acid, is a competitive inhibitor of the type I glycine transporter and an N-methyl-d-aspartate receptor (NMDAR) coagonist. Recently, we found that sarcosine, an NMDAR enhancer, can improve depression-related behaviors in rodents and humans. This result differs from previous studies, which have reported antidepressant effects of NMDAR antagonists. The mechanisms underlying the therapeutic response of sarcosine remain unknown. This study examines the role of mammalian target of rapamycin (mTOR) signaling and α-amino-3-hydroxy-5-methylisoxazole-4-propionate receptor (AMPAR) activation, which are involved in the antidepressant-like effects of several glutamatergic system modulators. The effects of sarcosine in a forced swim test (FST) and the expression levels of phosphorylated mTOR signaling proteins were examined in the absence or presence of mTOR and AMPAR inhibitors. In addition, the influence of sarcosine on AMPAR trafficking was determined by analyzing the phosphorylation of AMPAR subunit GluR1 at the PKA site (often considered an indicator for GluR1 membrane insertion in neurons). A single injection of sarcosine exhibited antidepressant-like effects in rats in the FST and rapidly activated the mTOR signaling pathway, which were significantly blocked by mTOR inhibitor rapamycin or the AMPAR inhibitor 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(f)quinoxaline (NBQX) pretreatment. Moreover, NBQX pretreatment eliminated the ability of sarcosine to stimulate the phosphorylated mTOR signaling proteins. Furthermore, GluR1 phosphorylation at its PKA site was significantly increased after an acute in vivo sarcosine treatment. The results demonstrated that sarcosine exerts antidepressant-like effects by enhancing AMPAR–mTOR signaling pathway activity and facilitating AMPAR membrane insertion. style="clear:both">Highlights class="first-line-outdent">– A single injection of sarcosine rapidly exerted antidepressant-like effects with a concomitant increase in the activation of the mammalian target of rapamycin mTOR signaling pathway.– The antidepressant-like effects of sarcosine occur through the activated AMPAR–mTOR signaling pathway.– Sarcosine could enhance AMPAR membrane insertion via an AMPAR throughput.
机译:肌氨酸是一种内源性氨基酸,是I型甘氨酸转运蛋白和N-甲基-d-天冬氨酸受体(NMDAR)激动剂的竞争性抑制剂。最近,我们发现肌氨酸钠是一种NMDAR增强剂,可以改善啮齿动物和人类的抑郁相关行为。该结果与以前的研究有所不同,之前的研究已经报道了NMDAR拮抗剂的抗抑郁作用。肌氨酸治疗反应的潜在机制仍然未知。这项研究检查了哺乳动物雷帕霉素靶标(mTOR)信号和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸酯受体(AMPAR)活化的作用,它们参与了几种谷氨酸能系统调节剂的抗抑郁样作用。在不存在或存在mTOR和AMPAR抑制剂的情况下,检查肌氨酸在强制游泳试验(FST)中的作用以及磷酸化mTOR信号蛋白的表达水平。此外,通过分析PKA位点的AMPAR亚基GluR1的磷酸化(通常被认为是神经元中GluR1膜插入的指标)来确定肌氨酸对AMPAR转运的影响。单次注射肌氨酸在FST大鼠中表现出抗抑郁样作用并迅速激活mTOR信号通路,而mTOR信号抑制剂雷帕霉素或AMPAR抑制剂2,3-二羟基-6-硝基-7-氨磺酰基-苯并呋喃可显着阻断mTOR信号通路。 (f)喹喔啉(NBQX)预处理。此外,NBQX预处理消除了肌氨酸刺激磷酸化的mTOR信号蛋白的能力。此外,急性体内肌氨酸治疗后,其PKA位点的GluR1磷酸化显着增加。结果表明,肌氨酸通过增强AMPAR–mTOR信号通路活性并促进AMPAR膜插入而发挥抗抑郁样作用。 style =“ clear:both”>亮点 class =“ first-line-outdent” > <!-list-behavior =简单的前缀-word = mark-type = none max-label-size = 9-> –肌氨酸的单次注射迅速发挥了抗抑郁样作用,并伴随着增加哺乳动物雷帕霉素靶标mTOR信号通路的激活。 –肌氨酸的抗抑郁样作用通过激活的AMPAR–mTOR信号通路发生。 –肌氨酸可以增强AMPAR膜的插入通过AMPAR吞吐量。

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