Generation of reactive oxygen species (ROS) by NADPH oxidase (NOX) contributes to brain damage during cerebral ischaemia. Researchers have now shown that proton flux through the voltage-gated proton channel Hv1 expressed on microglia supports NOX activity in mice. In a stroke model, trangenic mice lacking Hv1 showed lower infarct volumes and improved neurological scores compared with wild-type mice, together with reduced markers of cell death in the peri-infarct zone and lower ROS production.