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. 2019 Apr 2;14(4):e0214476. doi: 10.1371/journal.pone.0214476

Fig 1. Schematic illustration of the experimental design.

Fig 1

For the evaluation of plaque development, inflammation, ROS formation, and endothelial function ApoE-/- mice were used after 8 weeks of intraperitoneal application of NaSCN (200 μg every other day) or vehicle (DMSO). For the assessment of neointima formation wild-type mice were subjected to carotid artery wire injury, treated with NaSCN (200 μg every other day) or vehicle for 14 days, and then analyzed.