Howard Shanna L, Beaudin Stephane A, Strupp Barbara J, Smith Donald R
bioRxiv. 2023 Oct 4:2023.06.23.546356. doi: 10.1101/2023.06.23.546356.
Studies in children have reported associations between elevated manganese (Mn) exposure and ADHD-related symptoms of inattention, impulsivity/hyperactivity, and psychomotor impairment. Maternal choline supplementation (MCS) during pregnancy/lactation may hold promise as a protective strategy because it has been shown to lessen cognitive dysfunction caused by numerous early insults. Our objectives were to determine whether (1) developmental Mn exposure alters behavioral reactivity/emotion regulation, in addition to impairing learning, attention, impulse control, and sensorimotor function, and (2) MCS protects against these Mn-induced impairments. Pregnant Long-Evans rats were given standard diet, or a diet supplemented with additional choline throughout gestation and lactation (G3 - PND 21). Male offspring were exposed orally to 0 or 50 mg Mn/kg/day over PND 1-21. In adulthood, animals were tested in a series of learning, attention, impulse control, and sensorimotor tasks. Mn exposure caused lasting dysfunction in attention, reactivity to errors and reward omission, learning, and sensorimotor function, recapitulating the constellation of symptoms seen in ADHD children. MCS lessened Mn-induced attentional dysfunction and partially normalized reactivity to committing an error or not receiving an expected reward but provided no protection against Mn-induced learning or sensorimotor dysfunction. In the absence of Mn exposure, MCS produces lasting offspring benefits in learning, attention, and reactivity to errors. To conclude, developmental Mn exposure produces a constellation of deficits consistent with ADHD symptomology, and MCS offered some protection against the adverse Mn effects, adding to the evidence that maternal choline supplementation is neuroprotective for offspring and improves offspring cognitive functioning.
Developmental Mn exposure causes lasting dysfunction consistent with ADHD symptomology.Maternal choline supplementation (MCS) protects against Mn-induced deficits in attention and behavioral reactivity.MCS in control animals produces lasting benefits to offspring in learning, attention, and error reactivity.These data support efforts to increase choline intake during pregnancy, particularly for individuals at risk of neurotoxicant exposure.
针对儿童的研究报告了锰(Mn)暴露水平升高与注意力不集中、冲动/多动以及精神运动障碍等与多动症相关的症状之间的关联。孕期/哺乳期补充胆碱(MCS)可能是一种有前景的保护策略,因为已证明它能减轻由多种早期损伤引起的认知功能障碍。我们的目标是确定:(1)发育过程中的锰暴露除了损害学习、注意力、冲动控制和感觉运动功能外,是否还会改变行为反应性/情绪调节;(2)MCS能否预防这些由锰引起的损伤。怀孕的长 Evans 大鼠在整个妊娠期和哺乳期(妊娠第 3 天至出生后第 21 天)给予标准饮食或补充额外胆碱的饮食。雄性后代在出生后第 1 天至第 21 天经口给予 0 或 50 毫克锰/千克/天。成年后,对动物进行一系列学习、注意力、冲动控制和感觉运动任务测试。锰暴露导致注意力、对错误和奖励缺失的反应性、学习以及感觉运动功能出现持续功能障碍,重现了多动症儿童出现的一系列症状。MCS 减轻了锰引起的注意力功能障碍,并部分使对犯错或未获得预期奖励的反应正常化,但对锰引起的学习或感觉运动功能障碍没有提供保护。在没有锰暴露的情况下,MCS 对后代的学习、注意力和对错误的反应性产生持久益处。总之,发育过程中的锰暴露会产生一系列与多动症症状相符的缺陷,MCS 对锰的不良影响提供了一些保护,这进一步证明了孕期补充胆碱对后代具有神经保护作用并能改善后代认知功能。
发育过程中的锰暴露会导致与多动症症状相符的持续功能障碍。孕期补充胆碱(MCS)可预防锰引起的注意力和行为反应性缺陷。对照动物中的 MCS 对后代的学习、注意力和错误反应性产生持久益处。这些数据支持在孕期增加胆碱摄入量的努力,特别是对于有神经毒物暴露风险的个体。