青少年氟西汀暴露增加了成年雄性Sprague-Dawley大鼠前额皮质内erk相关信号。

Anapaula Themann, Minerva Rodriguez, Israel Garcia-Carachure, Omar Lira, Sergio D Iñiguez
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引用次数: 2

摘要

在青少年人群中氟西汀(FLX)处方率有不成比例的增加。因此,我们评估了青少年暴露于FLX如何改变成人前额叶皮质(PFC)内细胞外信号调节激酶(ERK)-1/2级联蛋白的表达/磷酸化。雄性Sprague-Dawley大鼠连续15天(出生后[PD] 35-49)暴露于FLX (20 mg/kg)。在PD70(成年)时,我们检测了ERK1/2、核糖体S6激酶(RSK)和哺乳动物雷帕霉素靶蛋白(mTOR)的蛋白标记物。flx预处理降低了体重,同时增加了PFC ERK1/2和RSK的磷酸化,以及成年期mTOR蛋白的总表达。我们提供的一线证据表明,青少年flx预处理诱导体重增加的长期下降,以及成人PFC的神经生物学变化——强调早期抗抑郁暴露会增加晚年的erk相关信号标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Adolescent fluoxetine exposure increases ERK-related signaling within the prefrontal cortex of adult male Sprague-Dawley rats.

There has been a disproportionate increase in fluoxetine (FLX) prescription rates within the juvenile population. Thus, we evaluated how adolescent FLX exposure alters expression/phosphorylation of proteins from the extracellular signal regulated kinase (ERK)-1/2 cascade within the adult prefrontal cortex (PFC). Male Sprague-Dawley rats were exposed to FLX (20 mg/kg) for 15 consecutive days (postnatal-day [PD] 35-49). At PD70 (adulthood), we examined protein markers for ERK1/2, ribosomal S6 kinase (RSK), and mammalian target of rapamycin (mTOR). FLX-pretreatment decreased body weight, while increasing PFC phosphorylation of ERK1/2 and RSK, as well as total mTOR protein expression in adulthood. We provide first-line evidence that juvenile FLX-pretreatment induces long-term decreases in body weight-gain, along with neurobiological changes in the adult PFC - highlighting that early-life antidepressant exposure increases ERK-related signaling markers in later life.

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