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大鼠发育性锰神经毒性:空间定位学习和记忆以及自我中心学习和记忆中的认知缺陷

Developmental manganese neurotoxicity in rats: Cognitive deficits in allocentric and egocentric learning and memory.

作者信息

Amos-Kroohs Robyn M, Davenport Laurie L, Atanasova Nina, Abdulla Zuhair I, Skelton Matthew R, Vorhees Charles V, Williams Michael T

机构信息

Division of Neurology, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, Cincinnati, OH 45229, United States.

Department of Environmental Health, University of Cincinnati, 3223 Eden Ave., Cincinnati, OH 45220, United States.

出版信息

Neurotoxicol Teratol. 2017 Jan-Feb;59:16-26. doi: 10.1016/j.ntt.2016.10.005. Epub 2016 Oct 15.

Abstract

Manganese (Mn) is an essential element but neurotoxic at higher exposure levels. The effects of Mn overexposure (MnOE) on hippocampal and striatal-dependent learning and memory in rats were tested in combination with iron deficiency (FeD) and developmental stress that often co-occur with MnOE. Moderate FeD affects up to 15% of U.S. children and developmental stress is common in lower socio-economic areas where MnOE occurs. Pregnant Sprague-Dawley rats and their litters were housed in cages with or without (barren cage (BAR)) standard bedding from embryonic day (E)7 to postnatal day (P)28. Dams were fed a 90% FeD or iron sufficient (FeS) diet from E15-P28. Within each litter, separate offspring were treated with 100mg/kg Mn (MnOE) or vehicle (VEH) by gavage on alternate days from P4-28. Offspring were tested as adults in the Morris and Cincinnati water mazes. FeD and developmental stress interactively impaired spatial learning in the Morris water maze. Developmental stress and MnOE impaired learning and memory in both mazes. MnOE resulted in reduced CA1 hippocampal long-term potentiation (LTP) and increased levels of α-synuclein. Preweaning MnOE resulted in cognitive deficits on multiple domains of learning and memory accompanied by impaired LTP and α-synuclein changes, effects worsened by developmental stress.

摘要

锰(Mn)是一种必需元素,但在高暴露水平时具有神经毒性。结合缺铁(FeD)和发育应激(这两种情况常与锰过度暴露(MnOE)同时出现),测试了MnOE对大鼠海马体和纹状体依赖性学习与记忆的影响。中度FeD影响高达15%的美国儿童,而发育应激在发生MnOE的低社会经济地区很常见。从胚胎期(E)7到出生后第(P)28天,将怀孕的斯普拉格-道利大鼠及其幼崽饲养在有或没有(贫瘠笼(BAR))标准垫料的笼子里。从E15到P28,给母鼠喂食90% FeD或铁充足(FeS)的饮食。在每一窝幼崽中,从P4到P28每隔一天通过灌胃给不同的幼崽施以100mg/kg锰(MnOE)或赋形剂(VEH)。成年后,在莫里斯水迷宫和辛辛那提水迷宫中对幼崽进行测试。FeD和发育应激在莫里斯水迷宫中交互性地损害空间学习能力。发育应激和MnOE在两个迷宫中均损害学习和记忆能力。MnOE导致海马体CA1区长期增强(LTP)降低以及α-突触核蛋白水平升高。断奶前的MnOE导致学习和记忆多个领域的认知缺陷,并伴有LTP受损和α-突触核蛋白变化,发育应激会使这些影响恶化。

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