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Migraine Monogenic familial hemiplegic migraine (FHM) type 2 is a primary genetic astrocytopathy caused by loss-of-function mutations in the ATP1A2 gene encoding the 2 subunit of Na + /K + ATPase (the NKA) expressed solely in astrocytes 327

As demonstrated by P7C3-A20 demonstrates hepatoprotective effects are a potential attribute of N-acetyltransferase, SBI-797812, and N-PAM, suggesting their possible therapeutic value in the treatment of fatty liver disease

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Drugs targeting neurons alone often fail because they ignore the reciprocal signaling that glia provide

Thus, the GSH/GSSG ratio reflects the oxidative state and can interact with redox couples to maintain appropriate redox balance in the cell