Department of Pharmacology, Universidade de Sao Paulo Instituto de Ciencias Biomedicas, Av. Prof. Lineu Prestes, 1524, room 323, São Paulo, SP, 05508-000, Brazil.
Central of Facilities, Universidade de Sao Paulo Instituto de Ciencias Biomedicas, São Paulo, 05508-000, Brazil.
Mol Neurobiol. 2021 Oct;58(10):4871-4885. doi: 10.1007/s12035-021-02470-2. Epub 2021 Jul 2.
The stress response is multifactorial and enrolls circuitries to build a coordinated reaction, leading to behavioral, endocrine, and autonomic changes. These changes are mainly related to the hypothalamus-pituitary-adrenal (HPA) axis activation and the organism's integrity. However, when self-regulation is ineffective, stress becomes harmful and predisposes the organism to pathologies. The chronic unpredictable stress (CUS) is a widely used experimental model since it induces physiological and behavioral changes and better mimics the stressors variability encountered in daily life. Corticotropin-releasing factor (CRF) and glucocorticoids (GCs) are deeply implicated in the CUS-induced physiological and behavioral changes. Nonetheless, the CUS modulation of CRF receptors and GR and the norepinephrine role in extra-hypothalamic brain areas were not well explored. Here, we show that 14 days of CUS induced a long-lasting HPA axis hyperactivity evidenced by plasmatic corticosterone increase and adrenal gland hypertrophy, which was dependent on both GCs and NE release induced by each stress session. CUS also increased CRF mRNA expression and GR protein levels in fundamental brain structures related to HPA regulation and behavior, such as the lateral septal nucleus intermedia part (LSI), ventromedial hypothalamic nucleus (VMH), and central nucleus of the amygdala (CeA). We also showed that NE participates in the CUS-induced increase in CRF and GR levels in the LSI, reinforcing the locus coeruleus (LC) involvement in the HPA axis modulation. Despite the CUS-induced molecular changes in essential areas related to anxiety-like behavior, this phenotype was not observed in CUS animals 24 h after the last stress session.
应激反应是多因素的,它会募集各种回路来构建一个协调的反应,导致行为、内分泌和自主神经系统的变化。这些变化主要与下丘脑-垂体-肾上腺(HPA)轴的激活和机体的完整性有关。然而,当自我调节无效时,应激就会变得有害,并使机体容易患上疾病。慢性不可预测应激(CUS)是一种广泛使用的实验模型,因为它会引起生理和行为的变化,并且更好地模拟了日常生活中遇到的应激源的可变性。促肾上腺皮质释放因子(CRF)和糖皮质激素(GCs)在 CUS 诱导的生理和行为变化中起着重要作用。然而,CUS 对 CRF 受体和 GR 的调节以及去甲肾上腺素在下丘脑外脑区的作用尚未得到充分探索。在这里,我们发现 14 天的 CUS 诱导了 HPA 轴的持久过度活跃,表现为血浆皮质酮的增加和肾上腺的肥大,这依赖于每个应激过程中 GC 和去甲肾上腺素的释放。CUS 还增加了与 HPA 调节和行为相关的基本脑结构中 CRF mRNA 表达和 GR 蛋白水平,如外侧隔核中间部分(LSI)、下丘脑腹内侧核(VMH)和杏仁中央核(CeA)。我们还表明,去甲肾上腺素参与了 CUS 诱导的 LSI 中 CRF 和 GR 水平的增加,强化了蓝斑核(LC)在 HPA 轴调节中的作用。尽管 CUS 诱导了与焦虑样行为相关的重要区域的分子变化,但在最后一次应激后 24 小时,CUS 动物中没有观察到这种表型。