Behavioral Alterations in Mice Exposed to Manganese via Drinking Water: Effects of Sex and a Lipopolysaccharide Challenge.

IF 2.7 4区 医学 Q3 TOXICOLOGY Journal of Applied Toxicology Pub Date : 2024-12-08 DOI:10.1002/jat.4739
Helaina D Ludwig, Jessica M Carpenter, Nikolay M Filipov
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Abstract

Manganese (Mn) is an essential and important metal; however, overexposures lead to adverse neurological outcomes. Nonoccupational Mn overexposure occurs primarily through consumption of Mn-contaminated drinking water (DW). Sex differences in terms of nervous and immune systems' responsiveness to excessive Mn in the DW are understudied. Thus, this study investigated behavioral and sex differences in response to Mn DW treatment (0.4 g Mn/L for up to 8 weeks) and a lipopolysaccharide (LPS) challenge of adult C57BL/6 mice with GFP-tagged monocytes/microglia. After 6 weeks, in motor function tests, Mn exposure resulted in decreased activity and gait deficits. In two different mood tests (open field test [OFT]/elevated zero maze), Mn-exposed mice exhibited decreased fear/anxiety-like behavior. Two weeks after behavioral assessment, when mice were challenged with LPS, circulating inflammatory cytokines, and acute phase proteins increased in both sexes. After 8 weeks of Mn exposure, liver and brain Mn levels were increased, but Mn alone did not affect circulating cytokines in either sex. Notably, Mn-exposed/LPS-challenged males had potentiated plasma cytokine output, whereas the reverse was seen in females. Males, but not females, continued to exhibit increased fearlessness (i.e., increased OFT center time), even when challenged with LPS. Overall, our results show that Mn DW exposure increases brain Mn levels and it leads to behavioral alterations in both sexes. However, males might be more susceptible to the effect of Mn on mood, and this effect is recalcitrant to an inflammagen challenge. Mn augmented post-LPS cytokine production only in males, further indicating that important Mn effects are sex-biased.

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通过饮用水暴露于锰的小鼠的行为改变:性别和脂多糖挑战的影响。
锰(Mn)是一种必需的重要金属;然而,过度暴露会导致不良的神经系统后果。非职业锰过量暴露主要是通过饮用受锰污染的饮用水(DW)发生的。在DW中,神经和免疫系统对过量Mn的反应性方面的性别差异尚未得到充分研究。因此,本研究调查了带有gfp标记的单核细胞/小胶质细胞的成年C57BL/6小鼠在Mn DW (0.4 g Mn/L,持续8周)和脂多糖(LPS)刺激下的行为和性别差异。6周后,在运动功能测试中,锰暴露导致活动减少和步态缺陷。在两种不同的情绪测试(开放场测试[OFT]/高架零迷宫)中,mn暴露小鼠表现出减少的恐惧/焦虑样行为。行为评估两周后,当小鼠受到LPS刺激时,循环炎症细胞因子和急性期蛋白在两性中均有所增加。暴露于锰8周后,肝脏和大脑锰水平升高,但锰单独不影响男女的循环细胞因子。值得注意的是,mn暴露/ lps挑战的男性有增强的血浆细胞因子输出,而在女性中则相反。男性,而不是女性,继续表现出增加的无畏性(即,增加的OFT中心时间),即使受到LPS的挑战。总的来说,我们的研究结果表明,Mn - DW暴露会增加大脑中的Mn水平,并导致两性的行为改变。然而,男性可能更容易受到锰对情绪的影响,而这种影响对炎症原的挑战是顽固的。Mn仅在男性中增加lps后细胞因子的产生,进一步表明Mn的重要作用是性别偏倚的。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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