Sensorimotor dysfunction due to developmental manganese exposure is less severe in adult female than male rats and partially improved by acute methylphenidate treatment

IF 2.6 3区 医学 Q3 NEUROSCIENCES Neurotoxicology and teratology Pub Date : 2024-02-01 DOI:10.1016/j.ntt.2024.107330
Stephane A. Beaudin , Samantha Gorman , Naomi Schilpp , David Woodfin , Barbara J. Strupp , Donald R. Smith
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Abstract

Epidemiological studies have reported associations between elevated manganese (Mn) exposure and poorer psychomotor performance in children. Our studies in adult male rats have established that this relationship is causal and that prolonged methylphenidate (MPH) treatment is efficacious in treating this area of dysfunction. However, it is unclear if sensitivity to these Mn deficits differs between females and males, and whether existing pharmacological therapies are efficacious in improving sensorimotor dysfunction in females. To address these questions, we used our rat model of childhood environmental Mn exposure and the Montoya staircase test to determine whether 1) there are sex differences in the lasting sensorimotor dysfunction caused by developmental Mn exposure, and 2) MPH treatment is efficacious in ameliorating the sensorimotor deficits in females. Female and male neonates were treated orally with Mn (50 mg Mn/kg/d) from postnatal day 1 to 21 and evaluated for skilled forelimb sensorimotor performance as adults. Subsequently, the efficacy of acute oral MPH treatment (doses of 0, 0.5, and 3.0 mg MPH/kg/d) was assessed in females using a within-subject MPH treatment design. Developmental postnatal Mn exposure produced lasting sensorimotor reaching and grasping deficits that were milder in females than in males. Acute MPH treatment of Mn-exposed females with the 0.5 mg/kg/d dose attenuated the reaching dysfunction without alleviating grasping dysfunction. These findings show sex-based variations in sensitivity to the sensorimotor impairment caused by developmental Mn exposure, and they are consistent with prior studies showing less vulnerability of females to Mn-induced dysfunction in other functional domains, possibly due to the protective effects of estrogen. Given our previous work showing the efficacy of MPH treatment to alleviate Mn-induced inattention, impulsiveness, and sensorimotor dysfunctions in adult male rats, they also highlight the need for further research into sex-based differences in cognitive and behavioral areas of brain function, and the efficacy of therapeutics in treating behavioral dysfunction in females.

Supported by NIEHS R01ES028369.

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与雄性大鼠相比,成年雌性大鼠因发育期接触锰而导致的感觉运动功能障碍并不严重,而且急性哌醋甲酯治疗可部分改善这种症状。
流行病学研究报告称,儿童锰(Mn)暴露量升高与精神运动表现较差之间存在关联。我们在成年雄性大鼠身上进行的研究证实,这种关系是因果关系,而且长期服用 MPH 可以有效治疗这方面的功能障碍。然而,目前还不清楚雌性和雄性对这些锰缺陷的敏感性是否不同,也不清楚现有的药物疗法对改善雌性的感觉运动功能障碍是否有效。为了解决这些问题,我们利用儿童环境锰暴露大鼠模型和蒙托亚阶梯测试来确定:1)发育期锰暴露导致的持久感觉运动功能障碍是否存在性别差异;2)哌醋甲酯(MPH)治疗是否能有效改善雌性大鼠的感觉运动功能障碍。雌性和雄性新生儿从出生后第1天到第21天口服锰(50毫克锰/千克/天),并在成年后对其熟练的前肢感觉运动能力进行评估。随后,采用受试者内MPH处理设计评估了急性口服MPH治疗(剂量为0、0.5和3.0 mg MPH/kg/d)对雌性的疗效。出生后锰暴露对雌性动物产生了持久的感觉运动伸手和抓握障碍,这种障碍比雄性动物轻微。对暴露于锰的雌性进行0.5 mg/kg/d剂量的急性MPH治疗可减轻伸手功能障碍,但不会减轻抓握功能障碍。这些研究结果表明,雌性对发育期锰暴露引起的感觉运动损伤的敏感性存在性别差异,这与之前的研究结果一致,之前的研究结果表明,雌性对锰引起的其他功能障碍的脆弱性较低,这可能是由于雌激素的保护作用。鉴于我们之前的研究显示 MPH 治疗能有效缓解锰诱导的成年雄性大鼠的注意力不集中、冲动和感觉运动功能障碍,这些研究也强调了进一步研究大脑功能的认知和行为领域的性别差异以及治疗雌性行为功能障碍的药物疗效的必要性。受美国国家卫生与健康研究所 R01ES028369 资助。
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来源期刊
CiteScore
5.60
自引率
10.30%
发文量
48
审稿时长
58 days
期刊介绍: Neurotoxicology and Teratology provides a forum for publishing new information regarding the effects of chemical and physical agents on the developing, adult or aging nervous system. In this context, the fields of neurotoxicology and teratology include studies of agent-induced alterations of nervous system function, with a focus on behavioral outcomes and their underlying physiological and neurochemical mechanisms. The Journal publishes original, peer-reviewed Research Reports of experimental, clinical, and epidemiological studies that address the neurotoxicity and/or functional teratology of pesticides, solvents, heavy metals, nanomaterials, organometals, industrial compounds, mixtures, drugs of abuse, pharmaceuticals, animal and plant toxins, atmospheric reaction products, and physical agents such as radiation and noise. These reports include traditional mammalian neurotoxicology experiments, human studies, studies using non-mammalian animal models, and mechanistic studies in vivo or in vitro. Special Issues, Reviews, Commentaries, Meeting Reports, and Symposium Papers provide timely updates on areas that have reached a critical point of synthesis, on aspects of a scientific field undergoing rapid change, or on areas that present special methodological or interpretive problems. Theoretical Articles address concepts and potential mechanisms underlying actions of agents of interest in the nervous system. The Journal also publishes Brief Communications that concisely describe a new method, technique, apparatus, or experimental result.
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