Brain inflammation holds promise as a therapeutic target in subacute stages of ischemic stroke. At the cellular level, postischemic inflammation is dominated by cells of the innate immune system with resident microglia/brain macrophages and blood-derived monocytes/macrophages being the most important cell types involved. Iron oxide nanoparticles such as ultrasmall superparamagnetic iron oxide (USPIO) are novel cell-specific contrast agents for MRI. After intravenous injection USPIO is taken up by circulating phagocytic cells. USPIO-laden macrophages cause typical signal changes in MRI of infarcted brain parenchyma, which has been demonstrated in studies of both experimental ischemia and human stroke. USPIO-enhanced MRI may therefore represent an important tool to address the role of macrophages for ischemic lesion development both in basic science and clinical studies. © 2007 American Heart Association, Inc.
Mendeley helps you to discover research relevant for your work.
CITATION STYLE
Jander, S., Schroeter, M., & Saleh, A. (2007). Imaging inflammation in acute brain ischemia. In Stroke (Vol. 38, pp. 642–645). https://doi.org/10.1161/01.STR.0000250048.42916.ad