Seno Soichiro, Tomura Satoshi, Miyazaki Hiromi, Sato Shunichi, Saitoh Daizoh
Division of Traumatology, Research Institute, National Defense Medical College, Saitama, Japan.
Division of Bioinformation and Therapeutic Systems, Research Institute, National Defense Medical College, Saitama, Japan.
Front Neurol. 2021 Feb 10;12:602038. doi: 10.3389/fneur.2021.602038. eCollection 2021.
Primary blast injury can result in depression-like behavior in the long-term. However, the effects of the selective serotonin reuptake inhibitor (SSRI) on the depression induced by mild blast traumatic brain injury (bTBI) in the long-term remain unclear. We generated a mouse model of mild bTBI using laser-induced shock wave (LISW) and administered an SSRI to mice by oral gavage for 14 days after LISW exposure. This study aimed to investigate the mechanisms of SSRI-mediated alleviation of depression-like behavior induced by mild bTBI. Animals were divided into three groups: sham, LISW-Vehicle, and LISW-SSRI. LISW was applied to the head of anesthetized mice at 0.5 J/cm. Twenty-eight days after the LISW, mice in the LISW-SSRI group exhibited reduced depression-like behavior, a significant increase in the number of cells co-stained for 5-bromo-2'-deoxyuridine (Brd-U) and doublecortin (DCX) in the dentate gyrus (DG) as well as increased brain-derived neurotrophic factor (BDNF) and serotonin levels in the hippocampus compared to the sham and LISW-Vehicle groups. Additionally, levels of phosphorylated cAMP response element binding protein (pCREB) in the DG were significantly decreased in the LISW-Vehicle group compared to that in the sham group. Importantly, pCREB levels were not significantly different between LISW-SSRI and sham groups suggesting that SSRI treatment may limit the downregulation of pCREB induced by mild bTBI. In conclusion, recovery from depression-like behavior after mild bTBI may be mediated by hippocampal neurogenesis induced by increased BDNF and serotonin levels as well as the inhibition of pCREB downregulation in the hippocampus.
原发性爆震伤长期可导致类似抑郁的行为。然而,选择性5-羟色胺再摄取抑制剂(SSRI)对轻度爆震性创伤性脑损伤(bTBI)所致抑郁的长期影响仍不清楚。我们使用激光诱导冲击波(LISW)建立了轻度bTBI小鼠模型,并在LISW暴露后通过灌胃给小鼠服用SSRI 14天。本研究旨在探讨SSRI介导的减轻轻度bTBI所致类似抑郁行为的机制。动物分为三组:假手术组、LISW-溶剂组和LISW-SSRI组。以0.5 J/cm的能量将LISW施加于麻醉小鼠头部。LISW后28天,与假手术组和LISW-溶剂组相比,LISW-SSRI组小鼠的类似抑郁行为减少,齿状回(DG)中5-溴-2'-脱氧尿苷(Brd-U)和双皮质素(DCX)共染色的细胞数量显著增加,海马中脑源性神经营养因子(BDNF)和5-羟色胺水平升高。此外,与假手术组相比,LISW-溶剂组DG中磷酸化环磷酸腺苷反应元件结合蛋白(pCREB)水平显著降低。重要的是,LISW-SSRI组和假手术组之间的pCREB水平无显著差异,表明SSRI治疗可能限制轻度bTBI诱导的pCREB下调。总之,轻度bTBI后类似抑郁行为的恢复可能是由BDNF和5-羟色胺水平升高诱导的海马神经发生以及海马中pCREB下调的抑制介导的。