Program in Molecular and Integrative Physiological Sciences, Department of Environmental Health, Harvard School of Public Health, 665 Huntington Avenue, Boston, MA 02115, United States.
Neurotoxicology. 2011 Aug;32(4):413-22. doi: 10.1016/j.neuro.2011.03.010. Epub 2011 Mar 31.
Manganese (Mn) and lead (Pb) exposures during developmental period can impair development by direct neurotoxicity or through interaction with iron metabolism. Therefore, we examined the effects of maternal ingestion of Mn or Pb in drinking water during gestation and lactation on iron metabolism as well as behavior in their offspring. Pregnant dams were given distilled water, 4.79mg/ml Mn, or 2.84mg/ml Pb in drinking water during gestation and lactation. Pups were studied at time of weaning for (59)Fe absorption from the gut, duodenal divalent metal transporter 1 (DMT1) expression, hematological parameters, and anxiety-related behavior using an Elevated Plus Maze (EPM) test. Metal-exposed pups had lower body weights and elevated blood and brain concentrations of the respective metal. Pb-exposed pups had lower hematocrits and higher blood Zn protoporphyrin levels. In contrast, Mn exposed pups had normal hematological parameters but significantly reduced Zn protoporphyrin. Pharmacokinetic studies using (59)Fe showed that intestinal absorption in metal-exposed pups was not different from controls, nor was it correlated with duodenal DMT1 expression. However, intravenously injected (59)Fe was cleared more slowly in Pb-exposed pups resulting in higher plasma levels. The overall tissue uptake of (59)Fe was lower in Mn-exposed and lower in the brain in Pb-exposed pups. The EPM test demonstrated that Mn-exposed, but not Pb-exposed, pups had lower anxiety-related behavior compared to controls. We conclude that gestational and lactational exposures to Mn or Pb differentially alter Fe metabolism and anxiety-related behavior. The data suggest that perturbation in Fe metabolism may contribute to the pathophysiologic consequences of Mn and Pb exposure during early development.
锰(Mn)和铅(Pb)在发育期间的暴露会通过直接神经毒性或与铁代谢相互作用来损害发育。因此,我们研究了母体在妊娠和哺乳期摄入饮用水中的 Mn 或 Pb 对其后代铁代谢和行为的影响。在妊娠和哺乳期,给怀孕的母鼠饮用蒸馏水、4.79mg/ml Mn 或 2.84mg/ml Pb。在断奶时,研究幼鼠从肠道吸收(59)Fe、十二指肠二价金属转运蛋白 1(DMT1)表达、血液学参数和焦虑相关行为(使用高架十字迷宫(EPM)测试)。暴露于金属的幼鼠体重较低,血液和大脑中各自金属的浓度升高。Pb 暴露的幼鼠的血细胞比容较低,血液锌原卟啉水平较高。相比之下,Mn 暴露的幼鼠血液学参数正常,但锌原卟啉显著减少。使用(59)Fe 进行的药代动力学研究表明,金属暴露幼鼠的肠道吸收与对照组无差异,也与十二指肠 DMT1 表达无关。然而,静脉注射的(59)Fe 在 Pb 暴露的幼鼠中清除速度较慢,导致血浆水平升高。(59)Fe 的总体组织摄取量在 Mn 暴露的幼鼠中较低,在 Pb 暴露的幼鼠中在大脑中较低。EPM 测试表明,Mn 暴露但不是 Pb 暴露的幼鼠的焦虑相关行为低于对照组。我们得出结论,妊娠和哺乳期暴露于 Mn 或 Pb 会以不同的方式改变 Fe 代谢和焦虑相关行为。这些数据表明,Fe 代谢的紊乱可能导致早期发育期间 Mn 和 Pb 暴露的病理生理后果。