Authors: James Blood, Nathan Sheets, Chase Seiter, Lydia Hawley, Erin Taylor, Eliza White, Hillary Wadsworth, Jason Hansen, Jordan Yorgason
Mentors: Jordan Yorgason
Insitution: Brigham Young University
Microglia are the immune cells of the brain and are activated by many drugs of abuse. One drug of abuse of interest is methamphetamine, which is known to increase reactive oxygen species (ROS). Microglia are sensitive to ROS. Methamphetamine changes microglia morphology. To determine if the effects of methamphetamine on microglia are through ROS, glucose oxidase, which reacts with glucose to form hydrogen peroxide, was applied. Glucose oxidase increased ROS production and decreased dopamine release but had little-to-no effect on ATP release. Glucose oxidase has similar effects on microglia morphology compared to methamphetamine. This suggests that methamphetamine effects on microglia are due to ROS production. Methamphetamine locomotor sensitization behavioral experiments were run to mimic repeated methamphetamine exposure. Along with voltammetry experiments to measure dopamine and ATP release, methamphetamine treated animals were used to detect microglial morphology changes using confocal microscopy. Our methamphetamine treatment was able to change microglial morphology compared to saline treated controls. Methamphetamine injected animals also had attenuated glucose oxidase effects on dopamine release. By understanding how neuronal outputs affect microglia activity in the context of psychostimulant use we can better parse out how the mechanisms of addiction are connected to immune system function.