Department of Molecular Biology and Endocrinology, "VINČA" Institute of Nuclear Sciences - National Institute of Thе Republic of Serbia, University of Belgrade, Belgrade, Serbia.
Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, 68159, Germany.
Brain Res Bull. 2021 Aug;173:174-183. doi: 10.1016/j.brainresbull.2021.05.021. Epub 2021 May 26.
The molecular background of depression is intensively studied in terms of alterations of inhibitory circuits, mediated by gamma aminobutyric acid (GABA) signalization. We investigated the effects of chronic social isolation (CSIS) and chronic fluoxetine (Flx) treatment (15 mg/kg/day) (3 weeks), on Parvalbumin (PV) and GAD67 expression in a layer-specific manner in rat dorsal hippocampal subregions. CSIS-induced depressive- and anxiety-like behaviours were confirmed with decrease in sucrose preference and increase in marble burying during behavioural testing, while Flx antagonized these effects. CSIS altered PV expression in stratum pyramidale (SP) of dorsal cornu ammonis 1 (dCA1) and stratum radiatum (SR) of dCA3. Flx antagonized this effect, and boosted PV expression in SP of the entire dCA and the dorsal dentate gyrus (dDG), as well as in the SR of dCA1/CA3. CSIS showed no significant effects on GAD67 expression, while Flx boosted its expression within the SR of the entire CA and SO of the dCA3. A correlation between SP of dCA1 and SR of dCA3 with regard to PV changes, implicates their possible role in the inhibitory circuit alterations. Flx-induced increase in GAD67 expression, specifically in SR of the entire dHIPP, may impose its involvement in the cell metabolic processes. Strong negative correlation between GAD67 and sucrose preference following Flx-treatment of CSIS rats was revealed. PV + cells of the SP layer of dCA1 and CA2 could be a potential target for the antidepressant action of Flx, while strong effect of Flx on GAD67 expression in the SR should be more extensively studied.
抑郁的分子生物学基础主要集中在γ-氨基丁酸(GABA)信号转导介导的抑制性回路的改变上。我们研究了慢性社会隔离(CSIS)和慢性氟西汀(Flx)治疗(15mg/kg/天)(3 周)对大鼠背侧海马亚区特定层中 Parvalbumin(PV)和 GAD67 表达的影响。CSIS 诱导的抑郁和焦虑样行为通过行为测试中蔗糖偏好减少和大理石掩埋增加来确认,而 Flx 拮抗这些效应。CSIS 改变了背角 1(dCA1)背角锥体层(SP)和 dCA3 辐射层(SR)中的 PV 表达。Flx 拮抗了这种作用,并增强了整个 dCA 和背侧齿状回(dDG)的 SP 以及 dCA1/CA3 的 SR 中的 PV 表达。CSIS 对 GAD67 表达没有显著影响,而 Flx 增强了整个 CA 的 SR 和 dCA3 的 SO 中的 GAD67 表达。关于 PV 变化,dCA1 的 SP 和 dCA3 的 SR 之间的相关性表明它们在抑制性回路改变中的可能作用。Flx 诱导的 GAD67 表达增加,特别是在整个 dHIPP 的 SR 中,可能表明其参与了细胞代谢过程。在 CSIS 大鼠经 Flx 治疗后,GAD67 与蔗糖偏好之间呈现强烈的负相关。dCA1 和 CA2 的 SP 层的 PV+细胞可能是 Flx 抗抑郁作用的潜在靶点,而 Flx 对 SR 中 GAD67 表达的强烈影响需要更广泛的研究。