“…As a membrane-permeable Ca 2+ chelator, BAPTA-AM could break the intracellular calcium homeostasis and inhibit Ca 2+ -mediated potassium ion channels, resulting in abnormal ion exchange inside and outside the cell. 40 Briefly, at low incubation concentrations (≤10 μmol L −1 ), BAPTA-AM had low cytotoxicity to cells, and the redox state in cells was stable. Therefore, the physiological function of cells was normal.…”