“…In fact, K ATP channel function has been quite extensively studied in several gastrointestinal models. The K ATP channel opener diazoxide has been shown to attenuate the damage and/or accelerate the restitution of indomethacin-and ethanol-induced intestinal and gastric injury in rats and mice (2,87,98,113,114,122,142), whereas K ATP channel inhibition worsened damage parameters. Moreover, the gastroprotective effect of different compounds, such as the steroid saponin hecogenin (122), the antidepressant drug citalopram (124), or prostaglandins (108), seems dependent on K ATP channel function.…”