Summary
Chronic low-level lead exposure has been demonstrated to inhibit neural cell acquisition and impair early postnatal structuring of the central nervous system. Lead was demonstrated to have an anti-mitotic action both in vitro and in vivo, although the latter was confined to the cerebellum at blood lead threshold values of 30–40 µg/dl. Low-level lead exposure more potently affected in vivo cell positioning and fibre outgrowth, as judged by the impaired developmental desialylation of the D2-CAM/N-CAM protein, and these effects were seen at blood lead threshold values of 20–30 µg/dl. This inhibition of normal D2-CAM/N-CAM desialylation is attributed to improper guidance of neuronal cells and their fibres, as lead is demonstrated to specifically induce precocious differentiation of the glial cells.
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Regan, C.M., Cookman, G.R., Keane, G.J., King, W., Hemmens, S.E. (1989). The Effects of Chronic Low-level Lead Exposure on the Early Structuring of the Central Nervous System. In: Smith, M.A., Grant, L.D., Sors, A.I. (eds) Lead Exposure and Child Development. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-0847-5_29
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DOI: https://doi.org/10.1007/978-94-009-0847-5_29
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