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Primers used for the experiment are listed in Additional file 8: Table S2

Vipadenant was investigated in an open-label, PET study and showed occupation of A2A receptors varying from 74 to 94 % in human brain regions, including the putamen, at the lowest daily dose of 2.5 mg, and reached saturation in all regions at 100 mg (Brooks et al

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focused on the proportion of corpus cavernosum cell death in STZ-induced T1DM rats and found ferroptosis in the corpus cavernosum tissue, endothelial cells, and smooth muscle cells under high-glucose conditions, while icariin improved erectile function in T1DM rats by suppressing oxidative stress and subsequently inhibiting ferroptosis, apoptosis, and pyroptosis in these cells [181]