| Literature DB >> 26276126 |
Nadine Hainz1, Sandra Wolf1, Thomas Tschernig1, Carola Meier2.
Abstract
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system. Neurological impairments are caused by axonal damage due to demyelination and neuroinflammation within the central nervous system. T cells mediate the neuroinflammation. The activation of T cells is induced by the release of adenosine triphosphate and involves purinergic receptors as well as pannexin (Panx) proteins. As Panx1 is expressed on T cells, we here propose that application of probenecid, a known Panx inhibitor, will prevent the onset of clinical symptoms in a mouse model of MS, the experimental autoimmune encephalomyelitis (EAE) model. EAE-induced mice received daily injections of probenecid. Disease scores, T cell numbers, and microglia activation were compared between experimental groups. Probenecid treatment resulted in lower disease scores as compared to EAE animals. Probenecid-treated animals also displayed fewer inflammatory lesions. Microglia activation was not altered by treatment. In conclusion, probenecid prevented the onset of EAE.Entities:
Keywords: multiple sclerosis; neuroinflammation; pannexin; probenecid
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Year: 2016 PMID: 26276126 DOI: 10.1007/s10753-015-0230-1
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092