Research Article

Activation of the Melanocortin-1 Receptor by NDP-MSH Attenuates Oxidative Stress and Neuronal Apoptosis through PI3K/Akt/Nrf2 Pathway after Intracerebral Hemorrhage in Mice

Figure 3

The administration of NDP-MSH improved neurological deficits and brain edema at 24 h after ICH. (a, b) Modified Garcia and beam balance scores showed intraperitoneal administration of NDP-MSH at the dose of 5 or 15 μg/mouse significantly reduced neurological deficits at 24 h after ICH. (c) NDP-MSH treatment attenuated the brain water content at 24 h after ICH. each group. Ipsilateral basal ganglia (ipsi-BG), contralateral basal ganglia (contra-BG), ipsilateral cortex (ipsi-CX), contralateral cortex (contra-CX), and cerebellum. # vs. sham group; vs. ICH + vehicle group.
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