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ABSTRACT: Background
Microglia initiates and sustains the inflammatory reaction that drives the pathogenesis of pneumococcal meningitis. The expression of the G-protein cannabinoid receptor type 2 (CB2) in the brain is low, but is upregulated in glial cells during infection. Its activation down-regulates pro-inflammatory processes, driving microglia towards an anti-inflammatory phenotype. CB2 agonists are therefore therapeutic candidates in inflammatory conditions like pneumococcal meningitis. We evaluated the effects of JWH-133, a specific CB2 agonist on microglial cells, inflammation, and damage driven by S. pneumoniae in vitro and in experimental pneumococcal meningitis.Materials/methods
Primary mixed glial cultures were stimulated with live or heat-inactivated S.
SUBMITTER: Pan SD
PROVIDER: S-EPMC7674855 | biostudies-literature | 2020
REPOSITORIES: biostudies-literature