Caffeine mitigates neuroinflammation and behavioral deficits induced by brain irradiation in mice.

IF 2.4
Mauricio M S Borges, Gabriel M Oliveira, Heitor G S Saraiva, Luciana P M Teixeira, Jhon B F Ferreira, Jemima F R Silva, Claudio S C Lau, Leonardo C Pacífico, André R C Barreto-Vianna, Penha C Barradas, Claudio C Filgueiras, Samara C Ferreira-Machado
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Abstract

Purpose: Radiotherapy, a standard treatment for brain tumors, may induce cognitive deficits and neuroinflammatory responses, including increased pro-inflammatory cytokines, microglial and astrocytic reactivity, and alterations in neuronal markers. Caffeine, a widely consumed psychostimulant with reported anti-inflammatory and neuroprotective properties, has been proposed as a potential modulator of these effects. This study evaluated whether continuous caffeine consumption is associated with attenuation of neuroinflammation, glial alterations, and behavioral impairments induced by brain irradiation in mice.

Materials and methods: Male C57BL/6J mice were assigned to four groups: non-irradiated control (C), irradiated (I), non-irradiated treated with caffeine (Ca), and irradiated treated with caffeine (ICa). Caffeine (0.25 g/L) was administered ad libitum for 94 days. Whole-brain irradiation (10 Gy) was delivered using a SARRP platform. Behavioral performance was assessed using the open-field, and object location memory tests. Immunofluorescence analyses for TNF-α, Iba1, GFAP, and NeuN were conducted in hippocampal subregions, and plasma TNF-α levels were quantified by ELISA.

Results: Irradiation impaired spatial memory, reduced locomotor activity, increased hippocampal TNF-α and GFAP immunolabeling, decreased Iba1 immunoreactivity, and reduced NeuN-positive neurons. In irradiated mice, caffeine consumption was associated with improved memory performance, preservation of locomotor activity, and attenuation of radiation-related changes in TNF-α, GFAP, Iba1, and NeuN immunolabeling. Plasma TNF-α levels did not differ across groups.

Conclusions: Continuous caffeine consumption was associated with reduced neuroinflammatory markers and modified glial and neuronal immunolabeling patterns, coinciding with improved behavioral outcomes in irradiated mice. This effect is interpreted as post-exposure mitigation rather than true regeneration.

咖啡因减轻小鼠脑辐照引起的神经炎症和行为缺陷。
目的:放疗是脑肿瘤的标准治疗方法,可诱导认知缺陷和神经炎症反应,包括促炎细胞因子、小胶质细胞和星形胶质细胞反应性增加,以及神经元标记物的改变。咖啡因是一种广泛使用的精神兴奋剂,据报道具有抗炎和神经保护作用,已被认为是这些作用的潜在调节剂。本研究评估了持续摄入咖啡因是否与小鼠脑辐照引起的神经炎症、神经胶质改变和行为损伤的衰减有关。材料与方法:雄性C57BL/6J小鼠分为四组:未辐照对照组(C)、辐照组(I)、未辐照咖啡因组(Ca)和咖啡因组(ICa)。咖啡因(0.25 g/L)随意给药94天。使用SARRP平台进行全脑照射(10 Gy)。行为表现评估使用开放领域和对象定位记忆测试。免疫荧光法检测海马亚区TNF-α、Iba1、GFAP和NeuN, ELISA法测定血浆TNF-α水平。结果:辐射损害了空间记忆,降低了运动活动,增加了海马TNF-α和GFAP免疫标记,降低了Iba1免疫反应性,减少了neun阳性神经元。在受辐射的小鼠中,咖啡因摄入与改善记忆表现、保持运动活动以及减弱TNF-α、GFAP、Iba1和NeuN免疫标记的辐射相关变化有关。血浆TNF-α水平各组间无差异。结论:持续摄入咖啡因与减少神经炎症标志物和改变神经胶质和神经元免疫标记模式有关,与辐照小鼠改善的行为结果相一致。这种影响被解释为暴露后的缓解,而不是真正的再生。
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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