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Ann N Y Acad Sci ; 1096: 179-83, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17405929

ABSTRACT

Oxidative brain damage, such as excitotoxicity and stroke, leads to primary neuronal destruction. The primary damage is further potentiated by macrophages and microglial cells, which are attracted and invade into the zone of damage resulting in secondary neuronal death. Since the essential trace element selenium has anti-inflammatory properties, we analyzed the effects of selenium on these inflammatory cells. Here, we show that the essential trace element selenium abrogates the stress-induced migration of microglial cells. Thus, the antimigratory effects of selenium may attenuate the secondary cell death cascade by preventing microglial invasion.


Subject(s)
Gene Expression Regulation , Macrophages/drug effects , Microglia/drug effects , Microglia/pathology , Selenium/pharmacology , Sodium Selenite/pharmacology , Animals , Anti-Inflammatory Agents/pharmacology , CD11a Antigen/biosynthesis , Cell Line , Cell Movement , Cell Separation , Hydrogen Peroxide/pharmacology , Inflammation , Mice , Microglia/metabolism , Neurons/metabolism
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