Suppr超能文献

长期给予法舒地尔对慢性应激雄性大鼠的抗抑郁相关行为及突触分子效应

Antidepressant-relevant behavioral and synaptic molecular effects of long-term fasudil treatment in chronically stressed male rats.

作者信息

Román-Albasini Luciano, Díaz-Véliz Gabriela, Olave Felipe Antonio, Aguayo Felipe Ignacio, García-Rojo Gonzalo, Corrales Wladimir Antonio, Silva Juan Pablo, Ávalos Ana María, Rojas Paulina S, Aliaga Esteban, Fiedler Jenny Lucy

机构信息

Laboratory of Neuroplasticity and Neurogenetics, Department of Biochemistry and Molecular Biology, Faculty of Chemical and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.

Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago, Chile.

出版信息

Neurobiol Stress. 2020 Jun 13;13:100234. doi: 10.1016/j.ynstr.2020.100234. eCollection 2020 Nov.

Abstract

Several lines of evidence suggest that antidepressant drugs may act by modulating neuroplasticity pathways in key brain areas like the hippocampus. We have reported that chronic treatment with fasudil, a Rho-associated protein kinase inhibitor, prevents both chronic stress-induced depressive-like behavior and morphological changes in CA1 area. Here, we examined the ability of fasudil to (i) prevent stress-altered behaviors, (ii) influence the levels/phosphorylation of glutamatergic receptors and (iii) modulate signaling pathways relevant to antidepressant actions. 89 adult male Sprague-Dawley rats received intraperitoneal fasudil injections (10 mg/kg/day) or saline vehicle for 18 days. Some of these animals were daily restraint-stressed from day 5-18 (2.5 h/day). 24 hr after treatments, rats were either evaluated for behavioral tests (active avoidance, anxiety-like behavior and object location) or euthanized for western blot analyses of hippocampal whole extract and synaptoneurosome-enriched fractions. We report that fasudil prevents stress-induced impairments in active avoidance, anxiety-like behavior and novel location preference, with no effect in unstressed rats. Chronic stress reduced phosphorylations of ERK-2 and CREB, and decreased levels of GluA1 and GluN2A in whole hippocampus, without any effect of fasudil. However, fasudil decreased synaptic GluA1 Ser831 phosphorylation in stressed animals. Additionally, fasudil prevented stress-decreased phosphorylation of GSK-3β at Ser9, in parallel with an activation of the mTORC1/4E-BP1 axis, both in hippocampal synaptoneurosomes, suggesting the activation of the AKT pathway. Our study provides evidence that chronic fasudil treatment prevents chronic stress-altered behaviors, which correlated with molecular modifications of antidepressant-relevant signaling pathways in hippocampal synaptoneurosomes.

摘要

多条证据表明,抗抑郁药物可能通过调节海马体等关键脑区的神经可塑性通路发挥作用。我们曾报道,用Rho相关蛋白激酶抑制剂法舒地尔进行长期治疗,可预防慢性应激诱导的抑郁样行为以及CA1区的形态变化。在此,我们研究了法舒地尔预防应激改变行为的能力、影响谷氨酸能受体水平/磷酸化的能力以及调节与抗抑郁作用相关的信号通路的能力。89只成年雄性Sprague-Dawley大鼠接受腹腔注射法舒地尔(10毫克/千克/天)或生理盐水,持续18天。其中一些动物从第5天至第18天每天接受束缚应激(2.5小时/天)。治疗24小时后,对大鼠进行行为测试(主动回避、焦虑样行为和物体位置测试),或者实施安乐死以进行海马体全提取物和富含突触神经小体部分的蛋白质免疫印迹分析。我们发现,法舒地尔可预防应激诱导的主动回避、焦虑样行为和新位置偏好受损,而对未应激的大鼠无影响。慢性应激降低了全海马体中ERK-2和CREB的磷酸化水平,并降低了GluA1和GluN2A的水平,法舒地尔对此无任何影响。然而,法舒地尔降低了应激动物突触中GluA1 Ser831的磷酸化水平。此外,法舒地尔还预防了应激导致的海马体突触神经小体中GSK-3β在Ser9位点的磷酸化水平降低,同时激活了mTORC1/4E-BP1轴,这表明AKT通路被激活。我们的研究提供了证据,表明长期使用法舒地尔治疗可预防慢性应激改变的行为,这与海马体突触神经小体中与抗抑郁相关信号通路的分子修饰有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59c6/7739043/1571a931a8a6/fx1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验