NADPH protects the post-stroke brain by activating the m6A demethylase FTO.

N6-methyladenosine (m6A) is the most pronounced epitranscriptomic modification of RNAs. Fat mass and obesity-associated (FTO) demethylates m6A-modified RNAs. Stroke reduces cerebral FTO expression, leading to increased abundance of m6A hypermethylated RNAs. FTO overexpression with a viral vector demethylates m6A-modified RNAs and improves post-stroke functional recovery. As NADPH activates FTO, we evaluated its therapeutic potential in a rodent stroke model. Adult and aged mice of both sexes were subjected to transient middle cerebral artery occlusion or photothrombotic ischemia, followed by intravenous administration of NADPH. FTO activity and m6A RNA methylation were measured enzymatically. NADPH efficacy and therapeutic window were assessed using sensorimotor and cognitive tests. Brain infarct volume, atrophy, and white matter damage were evaluated by MRI and histology analysis. Post-stroke administration of NADPH increased demethylase activity and reduced m6A-methylated RNA abundance, without altering FTO expression. NADPH treatment provided significant protection of gray and white matter, and better motor and cognitive recovery in both sexes, with a good therapeutic window and a low minimal efficacious dose. More importantly, FTO was also neuroprotective in aged mice subjected to stroke. These findings highlight NADPH as a promising post-stroke therapy that enhances FTO-mediated m6A RNA demethylation, leading to neuroprotection and functional recovery, irrespective of age and sex.