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. 2018 Jun 6;24:3804–3814. doi: 10.12659/MSM.907734

Figure 5.

Figure 5

Melatonin treatment upregulated SIRT3 expression caused by oxidative stress in the brain following subarachnoid hemorrhage (SAH). Three mouse groups were studied: the subarachnoid hemorrhage (SAH) group; the sham group; and the SAH + melatonin-treated group (intraperitoneal dose, 150 mg/kg). (A) Reduced glutathione (GSH), and its ratio with oxidized glutathione (GSSG) (the GSH: GSSG ratio) was inhibited in the SAH group, and melatonin treatment partially reversed the change in GSH: GSSG ratio induced by SAH. (B) Malonaldehyde (MDA) was significantly increased in the SAH group; MDA was significantly suppressed following treatment with melatonin.