FA mitigated OGD-induced oxidative and mitochondrial injury in Bend.3 cells and promoted angiogenesis-related responses through activation of the SIRT1/HIF-1α/VEGF-A axis. These data support a SIRT1-dependent endothelial protective mechanism and provide a rationale for future studies evaluating FA in neurovascular-unit systems and in vivo models relevant to Moyamoya disease.
Gao et al. (Mon,) studied this question.