Mesophyll K<sup>+</sup> retention ability has been recently reported as an important component of salinity stress tolerance in wheat. In order to investigate the role of ROS in regulating NaCl<sup>-</sup>induced K<sup>+</sup> efflux in wheat leaf mesophyll, a series of pharmacological experiments was conducted using MV (methyl viologen, superoxide radical inducer), DPI (an inhibitor of NADPH oxidase), H<sub>2</sub>O<sub>2</sub> (to mimic apoplastic ROS), and EGCG ((−)-Epigallocatechin gallate, ROS scavenger). Mesophyll pre-treatment with 10 μM MV resulted in a significantly higher NaCl<sup>-</sup>induced K<sup>+</sup> efflux in leaf mesophyll, while 50 μM EGCG pre-treatment alleviated K<sup>+</sup> leakage under salt stress. No significant change in NaCl<sup>-</sup>induced K<sup>+</sup> efflux in leaf mesophyll was found in specimens pre-treated by H<sub>2</sub>O<sub>2</sub> and DPI, compared with the control. The highest NaCl<sup>-</sup>induced H<sup>+</sup> efflux in leaf mesophyll was also found in samples pre-treated with MV, suggesting a futile cycle between increased H<sup>+</sup>-ATPase activity and ROS-induced K<sup>+</sup> leak. Overall, it is suggested that, under saline stress, K<sup>+</sup> efflux from wheat mesophyll is mediated predominantly by non-selective cation channels (NSCC) regulated by ROS produced in chloroplasts, at least in bread wheat.