Summary
This study tested whether daily low-dose THC during adolescence persistently changes microglia in male and female mice. Exposure produced broad disruption of homeostatic and innate-immune gene programs in young adulthood and weakened microglial responses to bacterial endotoxin and repeated social stress; the effects receded with age and were prevented by blocking CB1 receptors. UID UCT-2112 temperature microchips and a URH-1HP reader supported monitoring and identification.
Summary written by UID from the published work. Read the original publication for the authors' abstract and full methods.