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在存在和不存在帕金森病前期的情况下,亚慢性锰暴露的神经行为学效应。

The neurobehavioral effects of subchronic manganese exposure in the presence and absence of pre-parkinsonism.

作者信息

Witholt R, Gwiazda R H, Smith D R

机构信息

Environmental Toxicology, Applied Sciences Building, University of California, 1156 High Street, Santa Cruz, CA 95064, USA.

出版信息

Neurotoxicol Teratol. 2000 Nov-Dec;22(6):851-61. doi: 10.1016/s0892-0362(00)00108-2.

Abstract

Recent studies have implicated chronic elevated exposures to environmental agents, such as metals (e.g., manganese, Mn) and pesticides, as contributors to neurological disease. In particular, there is a concern that sensitive subpopulations such as the aged may be at increased risk for the onset of neurologic disorders because elevated exposures to Mn is associated with increased incidence of parkinsonism. Here, we utilized a rat model of pre-parkinsonism to investigate the effects of Mn exposure on neurotoxicity and the exacerbation of parkinsonism. A pre-parkinsonism state was induced using a unilateral intrastriatal injection of 6-hydroxydopamine (6-OHDA), followed 4 weeks later by Mn exposure (4.8 mg Mn/kgx3 intraperitoneal injections/week) for 5 weeks. Female Sprague-Dawley rats (n=44) were divided among the following treatments: (A) control, saline/vehicle; (B) Mn only; (C) 6-OHDA only; and (D) 6-OHDA+Mn. Brain Mn levels were measured by ICP-MS. Neurobehavioral function was assessed following Mn exposure using a functional observational battery (FOB) consisting of 10 neurobehavioral tests. Unilateral 6-OHDA lesions produced significant ipsilateral vs. contralateral striatal dopamine depletions (60-70%), but no measurable impairment of neurobehavioral function, thereby substantiating this pre-parkinsonism (i.e., subthreshold) model. In contrast, Mn exposure resulted in significant impairment of neurobehavioral function for eight of the 10 FOB tests. No effects of Mn exposure on striatal dopamine depletion were detected, despite the 3.4-fold increase in brain Mn levels over controls. Notably, Mn exposure in the presence of a pre-parkinsonism state significantly exacerbated the neurobehavioral impairment in the reactivity to handling (P<.049) and hopping contralateral rear limb (P<.033) FOB tests. While the persistence and Mn dose-response relationship of these neurobehavioral effects were not evaluated here, these results nonetheless suggest that chronic Mn exposure may increase the risk of neurobehavioral impairment in subpopulations that are in a pre-parkinsonism state.

摘要

最近的研究表明,长期暴露于环境因素,如金属(如锰,Mn)和农药,会导致神经疾病。特别是,人们担心老年人等敏感亚群可能患神经疾病的风险增加,因为长期接触锰与帕金森病发病率增加有关。在这里,我们利用帕金森病前期大鼠模型来研究锰暴露对神经毒性和帕金森病加重的影响。通过单侧纹状体内注射6-羟基多巴胺(6-OHDA)诱导帕金森病前期状态,4周后进行锰暴露(4.8mg Mn/kg,每周3次腹腔注射),持续5周。将雌性Sprague-Dawley大鼠(n = 44)分为以下几组进行处理:(A)对照组,生理盐水/赋形剂;(B)仅锰处理组;(C)仅6-OHDA处理组;(D)6-OHDA + 锰处理组。通过电感耦合等离子体质谱法(ICP-MS)测量脑锰水平。在锰暴露后,使用由10项神经行为测试组成的功能性观察组合(FOB)评估神经行为功能。单侧6-OHDA损伤导致同侧与对侧纹状体多巴胺显著耗竭(60 - 70%),但未观察到神经行为功能的可测量损伤,从而证实了这个帕金森病前期(即亚阈值)模型。相比之下,在10项FOB测试中的8项中,锰暴露导致神经行为功能显著受损。尽管脑锰水平比对照组增加了3.4倍,但未检测到锰暴露对纹状体多巴胺耗竭的影响。值得注意的是,在帕金森病前期状态下的锰暴露显著加剧了在处理反应性(P <.049)和对侧后肢跳跃(P <.033)FOB测试中的神经行为损伤。虽然这里没有评估这些神经行为效应的持续性和锰剂量反应关系,但这些结果仍然表明,长期锰暴露可能会增加处于帕金森病前期状态的亚群中神经行为损伤的风险。

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