State Key Laboratory of Pollution Control and Resources Reuse, School of the Environment, Nanjing University, Nanjing 210023, China.
School of the Chemical Engineering, Huaiyin Institute of Technology, Huaian 223003, China.
Toxicol Sci. 2018 Jul 1;164(1):278-288. doi: 10.1093/toxsci/kfy086.
Particulate matter (PM) exposure may contribute to depressive-like response in mice. However, few studies have evaluated the adaptive impacts of long-term PM exposure on depressive-like response associated with systemic inflammation and brain-derived neurotrophic factor (BDNF) signaling pathway. We studied the association among depressive-like behaviors, mRNA levels of pro and anti-inflammatory cytokines, and the expression of BDNF signaling pathway in mice by long-term PM exposure. C57BL/6 male mice were exposed to ambient air alongside control mice breathing air filtered through a high-efficiency air PM (HEPA) filter. Depressive-like behaviors were assessed together with proinflammatory, anti-inflammatory cytokine mRNA levels and the modulation of BDNF pathway in hippocampus and olfactory-bulb of mice exposed to PM for 4, 8, and 12 weeks. Exposure to HEPA-filtered air for 4 weeks may exert antidepressant like effects in mice. Proinflammatory cytokines were up-regulated while the expression of BDNF, its high-affinity receptor tropomyosin-related kinase B (TrkB), and the transcription factor (cyclic adenosine monophosphate)-response element-binding protein (CREB) were down-regulated in ambient air mice. However, after 8 weeks, there was no significant difference in the rate of depressive-like behaviors between the 2 groups. After 12 weeks, mice exposed to ambient air again had a higher rate of depressive-like behaviors, significant up-regulation of proinflammatory cytokines, down-regulation of interleukin-10, BDNF, TrkB, and CREB than HEPA mice. Ultrafine PM in brain tissues of mice exposed to ambient air was observed. Our results suggest continuous high-level PM exposure alters the depressive-like response in mice and induces a damage-repair-imbalance reaction.
颗粒物 (PM) 暴露可能导致小鼠出现类似抑郁的反应。然而,很少有研究评估长期 PM 暴露对与全身炎症和脑源性神经营养因子 (BDNF) 信号通路相关的类似抑郁反应的适应性影响。我们通过长期 PM 暴露研究了小鼠类似抑郁行为、促炎和抗炎细胞因子的 mRNA 水平以及 BDNF 信号通路表达之间的关系。将 C57BL/6 雄性小鼠暴露于环境空气中,同时将呼吸经过高效空气 PM(HEPA)过滤器过滤的空气的对照小鼠置于其中。评估了暴露于 PM 的小鼠 4、8 和 12 周后的类似抑郁行为、促炎细胞因子的 mRNA 水平以及海马体和嗅球中 BDNF 通路的调节。暴露于 HEPA 过滤器空气 4 周可能对小鼠具有抗抑郁作用。在环境空气小鼠中,促炎细胞因子上调,而 BDNF、其高亲和力受体原肌球蛋白相关激酶 B (TrkB) 和转录因子(环腺苷酸单磷酸)-反应元件结合蛋白 (CREB) 的表达下调。然而,8 周后,两组之间类似抑郁行为的发生率没有显著差异。12 周后,再次暴露于环境空气中的小鼠出现了更高的类似抑郁行为发生率,促炎细胞因子显著上调,白细胞介素-10、BDNF、TrkB 和 CREB 下调,高于 HEPA 小鼠。在暴露于环境空气的小鼠脑组织中观察到超细 PM。我们的研究结果表明,持续高水平的 PM 暴露改变了小鼠的类似抑郁反应,并诱导了损伤-修复-失衡反应。