Rudyk Chris, Dwyer Zach, McNeill Jessica, Salmaso Natalina, Farmer Kyle, Prowse Natalie, Hayley Shawn
Department of Neuroscience, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario, Canada, K1S 5B6.
Department of Neurology, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Neurobiol Stress. 2019 May 31;11:100179. doi: 10.1016/j.ynstr.2019.100179. eCollection 2019 Nov.
The impact of psychological stressors on the progression of motor and non-motor disturbances observed in Parkinson's disease (PD) has received little attention. Given that PD likely results from many different environmental "hits", we were interested in whether a chronic unpredictable stressor regimen would act additively or possibly even synergistically to augment the impact of the toxicant, paraquat, which has previously been linked to PD. Our findings support the contention that paraquat itself acted as a systemic stressor, with the pesticide increasing plasma corticosterone, as well as altering glucocorticoid receptor (GR) expression in the hippocampus. Furthermore, stressed mice that also received paraquat displayed synergistic motor coordination impairment on a rotarod test and augmented signs of anhedonia (sucrose preference test). The individual stressor and paraquat treatments also caused a range of non-motor (e.g. open field, Y and plus mazes) deficits, but there were no signs of an interaction (neither additive nor synergistic) between the insults. Similarly, paraquat caused the expected loss of substantia nigra dopamine neurons and microglial activation, but this effect was not further influenced by the chronic stressor. Taken together, these results indicate that paraquat has many effects comparable to that of a more traditional stressor and that at least some behavioral measures (i.e. sucrose preference and rotarod) are augmented by the combined pesticide and stress treatments. Thus, although psychological stressors might not necessarily increase the neurodegenerative effects of the toxicant exposure, they may promote co-morbid behaviors pathology.
心理应激源对帕金森病(PD)中观察到的运动和非运动障碍进展的影响很少受到关注。鉴于PD可能由许多不同的环境“打击”导致,我们感兴趣的是,慢性不可预测应激源方案是否会产生累加作用,甚至可能产生协同作用,以增强先前与PD相关的毒物百草枯的影响。我们的研究结果支持这样的观点,即百草枯本身作为一种全身性应激源,这种农药会增加血浆皮质酮水平,并改变海马体中糖皮质激素受体(GR)的表达。此外,同时接受百草枯处理的应激小鼠在转棒试验中表现出协同性运动协调障碍,并在快感缺失测试(蔗糖偏好测试)中出现增强的症状。单独的应激源处理和百草枯处理也导致了一系列非运动方面的缺陷(如旷场试验、Y迷宫试验和十字迷宫试验),但在这些损伤之间没有相互作用的迹象(既没有累加作用也没有协同作用)。同样,百草枯导致了黑质多巴胺能神经元的预期损失和小胶质细胞激活,但这种效应并未受到慢性应激源的进一步影响。综上所述,这些结果表明,百草枯具有许多与更传统应激源相当的作用,并且至少一些行为指标(即蔗糖偏好和转棒试验)在农药和应激联合处理下会增强。因此,虽然心理应激源不一定会增加毒物暴露的神经退行性影响,但它们可能会促进共病行为病理学的发展。