Department of Environmental Medicine, University of Rochester, Rochester, New York 14642, USA.
Department of Microbiology and Immunology, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14642, USA.
Toxicol Sci. 2021 Feb 26;180(1):175-185. doi: 10.1093/toxsci/kfaa183.
Epidemiological and experimental studies have associated oral and systemic exposures to the herbicide paraquat (PQ) with Parkinson's disease. Despite recognition that airborne particles and solutes can be directly translocated to the brain via olfactory neurons, the potential for inhaled PQ to cause olfactory impairment has not been investigated. This study sought to determine if prolonged low-dose inhalation exposure to PQ would lead to disposition to the brain and olfactory impairment, a prodromal feature of Parkinson's disease. Adult male and female C57BL/6J mice were exposed to PQ aerosols in a whole-body inhalation chamber for 4 h/day, 5 days/week for 4 weeks. Subsets of mice were sacrificed during and after exposure and PQ concentrations in various brain regions (olfactory bulb, striatum, midbrain, and cerebellum) lung, and kidney were quantified via mass spectrometry. Alterations in olfaction were examined using an olfactory discrimination paradigm. PQ inhalation resulted in an appreciable burden in all examined brain regions, with the highest burden observed in the olfactory bulb, consistent with nasal olfactory uptake. PQ was also detected in the lung and kidney, yet PQ levels in all tissues returned to control values within 4 weeks post exposure. PQ inhalation caused persistent male-specific deficits in olfactory discrimination. No effects were observed in females. These data support the importance of route of exposure in determination of safety estimates for neurotoxic pesticides, such as PQ. Accurate estimation of the relationship between exposure and internal dose is critical for risk assessment and public health protection.
流行病学和实验研究表明,除草剂百草枯(PQ)的口腔和全身暴露与帕金森病有关。尽管人们认识到空气传播的颗粒和溶质可以通过嗅觉神经元直接转移到大脑,但吸入的 PQ 是否会导致嗅觉障碍尚未得到研究。本研究旨在确定长期低剂量吸入 PQ 是否会导致大脑易感性增加和嗅觉障碍,这是帕金森病的前驱特征。成年雄性和雌性 C57BL/6J 小鼠在全身吸入室中每天暴露于 PQ 气溶胶 4 小时,每周 5 天,持续 4 周。在暴露期间和之后,对部分小鼠进行了牺牲,并用质谱法定量了各种大脑区域(嗅球、纹状体、中脑和小脑)、肺和肾中的 PQ 浓度。使用嗅觉辨别范式检查嗅觉改变。PQ 吸入导致所有检查的大脑区域都有明显的负担,嗅球中的负担最高,与鼻内嗅觉吸收一致。PQ 也在肺和肾脏中被检测到,但暴露后 4 周内所有组织中的 PQ 水平均恢复到对照值。PQ 吸入导致雄性特有的嗅觉辨别持续缺陷。在雌性中未观察到任何影响。这些数据支持暴露途径在确定神经毒性农药(如 PQ)的安全性估计中的重要性。准确估计暴露与内部剂量之间的关系对于风险评估和公共卫生保护至关重要。