For HIF‐1α inhibition, mice were administered PX‐478 (5 mg/kg,
HY‐10231, MedChemExpress) in phosphate‐buffered saline (PBS) solution by oral gavage every other day, and the control mice received an equivalent amount of PBS. For NLRP3 inhibition, mice were gavaged with MCC950 (20 mg/kg,
HY‐12815, MedChemExpress) or vehicle (.9% NaCl) every day for 5 days/week. For Drp1 inhibition, mice were given mitochondrial division inhibitor 1 (Mdivi‐1) (20 mg/kg, dissolved in dimethyl sulfoxide (DMSO),
HY‐15886, MedChemExpress) intraperitoneally, and the control mice were injected with the same volume of DMSO. For ROS scavenging, mice were intraperitoneally injected with mito‐TEMPO (MT, dissolved in PBS, 10 mg/kg,
HY‐112879, MedChemExpress) every other day, and the mice in the control group were given an equal volume of PBS intraperitoneally.
Xiao Y., Liu X., Xie K., Luo J., Zhang Y., Huang X., Luo J, & Tan S. (2024). Mitochondrial dysfunction induced by HIF‐1α under hypoxia contributes to the development of gastric mucosal lesions. Clinical and Translational Medicine, 14(4), e1653.