However, Mn over exposure (MnOE), most commonly seen in adults from occupational exposure, can produce symptoms similar to Parkinson’s disease (manganism), especially motor deficits [1], [2] and [3]. Cognitive and other behavioral deficits also occur [4] and [5]. This phenotype is seen in rodent models of MnOE as well. For instance, MnOE results in spatial working memory deficits and increases in compulsive behaviors

in non-human primates [6] and in spatial memory deficits in rodents in the Morris water maze [7]. MnOE also has effects when it occurs during development [8] that include deficits in executive function and passive avoidance [9]. Neonatal rats accumulate Mn more than similarly isocitrate dehydrogenase signaling pathway exposed adults because of lower excretion shortly after birth (postnatal day (P) 8-10) compared with later time points (P18-19); however, even P18-19 rats excrete Mn at lower rates than adults [10], [11] and [12]; this developmental pattern is mediated in part by reduced biliary excretion of Mn during the preweaning period [13], [14] and [15]. 54MnCl2 tracer analysis

in rats found that Mn uptake was highest in brain (with regional specificity), followed by liver and blood. Developmentally, the highest uptake is at P5 compared with other ages from 5 weeks to almost 2 years of age [16]. Physiologically-based pharmacokinetic modeling in rats verifies the above findings and the higher Mn uptake in the neonatal period is likely because of higher Mn requirements during rapid growth as seen during the preweaning Entinostat cost period [17]. This leaves open the question of whether the same developmental mechanisms that permit greater Mn uptake for nutritional requirements may act to increase exposure when Mn levels are increased beyond what is nutritionally needed.

www.selleck.co.jp/products/Paclitaxel(Taxol).html Ingestion of excess Mn in children occurs for a number of reasons, including, but not limited to infant baby formulas or polluted air, soil, or well water. MnOE children show cognitive deficits, behavioral disinhibition, decreased IQ, and decreased performance on school-related tasks [18], [19], [20], [21] and [22]. Soy-based baby formula ([23] and [9]) can contain 5, 10, or more times the levels of Mn found in cow-based formulas and 100 times or more than found in human breast milk [1], [24] and [25]. Unfortunately, one of the factors that makes soy-based formulas attractive is that they are often less expensive. Thus, children in lower socioeconomic status (SES) families are more likely to be fed soy-based formulas, and this is in addition to having a greater risk for exposure to stress because of the impoverished environments associated with lower SES. The combination of MnOE and stress during development may interact to create greater risk than either factor alone. Chronic stress is a known risk factor to the developing nervous system.