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Endocr J (2016) 63:88595

Using the homologous sequence search, we identified glutathione biosynthetic enzymes (Gcs1 and Gcs2), glutathione peroxidase (Gpx1), glutathione reductase (Glr1), and a family of glutathione S-transferases (Gsts)

Upregulation of NFB signaling pathways can activate MMP-9 [374], leading to increased mitochondrial MMP-9, which damages the mitochondrial gap junction protein connexin-43 and further enhances pore permeability

7) consists of a thioredoxin reductase homologue with specificity for NADH (Cp34) and a Grx homologue (Cp9) that requires no glutathione (a LMW thiol that is not present in C