The melatonin receptor antagonist luzindole induces Ca mobilization, reactive oxygen species generation and impairs trypsin secretion in mouse pancreatic acinar cells.

Background: In this work we studied the effects of the melatonin receptor-antagonist luzindole (1 μM-50 μM) on isolated mouse pancreatic acinar cells.

Methods: Changes in intracellular free-Ca concentration, reactive oxygen species production and trypsin secretion were analyzed.

Results: Luzindole induced increases in [Ca] that diminished CCK-8 induced Ca mobilization, compared with that observed when CCK-8 was applied alone. Treatment of cells with thapsigargin (1 μM), in the absence of Ca in the extracellular medium, evoked a transient increase in [Ca]. The additional incubation of cells with luzindole (10 μM) failed to induce further mobilization of Ca. In the presence of luzindole a concentration-dependent increase in ROS generation was observed that decreased in the absence of Ca or by pretreatment of cells with melatonin (100 μM). Incubation of pancreatic acinar cells with luzindole (10 μM) impaired CCK-8-induced trypsin secretion. Melatonin was unable to revert the effect of luzindole on CCK-8-induced trypsin secretion.

Conclusion: The melatonin receptor-inhibitor luzindole induces Ca-mediated pro-oxidative conditions and impairment of enzyme secretion, which creates a situation in pancreatic acinar cells that might compromise their function.

General Significance: The effects of luzindole that we have observed, might be unspecific and could mislead the observations when it is used to study the actions of melatonin on the gland. Another possibility is that melatonin receptors exhibit a basal or agonist-independent activity in pancreatic acinar cells, which might be modulated by melatonin or luzindole.