Neuroinflammation is initiated by many types of neural disorders as a defensive response of the innate immune system in the central nervous system (CNS). Neuroinflammation is typically accompanied by the disruption of Ca2+ homeostasis. Manganese chloride (MnCl2) is a useful positive MRI contrast agent that enters activated cells through Ca2+ channels, and is utilized in Manganese-Enhanced MRI (MEMRI) for functional neuroimaging. We sought to determine whether MEMRI could be used to assess the cellular/molecular alterations caused by acute neuroinflammation in vivo, by focusing on Mn2+ accumulation in the rodent brain.
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