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Neurobiol Aging. 2006 Dec;27(12):1816-26. Epub 2005 Nov 14.

Determining the oxidation states of manganese in NT2 cells and cultured astrocytes.

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  • 1Department of Biochemistry and Biophysics, University of Rochester School of Medicine and Dentistry, 575 Elmwood Ave., Rochester, NY 14642, USA. karlene_gunter@urmc.rochester.edu <karlene_gunter@urmc.rochester.edu>

Abstract

Excessive brain manganese (Mn) can produce a syndrome called "manganism", which correlates with loss of striatal dopamine and cell death in the striatum and globus pallidus. The prevalent hypothesis for the cause of this syndrome has been oxidation of cell components by the strong oxidizing agent, Mn(3+), either formed by oxidation of intracellular Mn(2+) or transported into the cell as Mn(3+). We have recently used X-ray absorption near edge structure spectroscopy (XANES) to determine the oxidation states of manganese complexes in brain and liver mitochondria and in nerve growth factor (NGF)-induced and non-induced PC12 cells. No evidence was found for stabilization or accumulation of Mn(3+) complexes because of oxidation of Mn(2+) by reactive oxygen species in these tissues. Here we extend these studies of manganese oxidation state to cells of brain origin, human neuroteratocarcinoma (NT2) cells and primary cultures of rat astrocytes. Again we find no evidence for stabilization or accumulation of any Mn(3+) complex derived from oxidation of Mn(2+) under a range of conditions.

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