For example, it has been shown to promote axonal growth in retinal ganglion cells [69], reduce hypersensitization of Piezo1 channels in astrocytes under neuroinflammatory conditions [70, 71], preserve neuronal survival after intracerebral hemorrhage [72], and mitigate autophagy overactivation caused by sleep deprivation to protect cognitive functions in the basal forebrain [73]. This evidence concerns the gene PIEZO1 and intracerebral hemorrhage.