To explore the effect of nortriptyline, a tricyclic antidepressant, on cytosolic free Ca(superscript 2+) concentrations ([Ca(superscript 2+)](subscript i)) in corneal epithelial cells, [Ca(superscript 2+)](subscript i) levels in suspended SIRC rabbit corneal epithelial cells were measured by using fura-2 as a Ca(superscript 2+)-sensitive fluorescent dye. Nortriptyline at concentrations between 20-200 μM increased [Ca(superscript 2+)](subscript i) in a concentration-dependent manner. The Ca(superscript 2+) signal was reduced partly by removing extracellular Ca(superscript 2+). Nortriptyline-induced Ca(superscript 2+) influx was inhibited by the store-operated Ca(superscript 2+) channel blockers econazole and SK&F96365, the phospholipase A2 inhibitor aristolochic acid, and alteration of activity of protein kinase C. In Ca(superscript 2+)-free medium, 200μM nortriptyline pretreatment greatly inhibited the rise of [Ca(superscript 2+)](subscript i) induced by the endoplasmic reticulum Ca(superscript 2+) pump inhibitor thapsigargin. Conversely, pretreatment with thapsigargin or 2, 5-di-tert-butylhydroquinone (BHQ; another endoplasmic reticulum Ca(superscript 2+) pump inhibitor) nearly abolished nortriptyline-induced [Ca(superscript 2+)](subscript i) rise. Inhibition of phospholipase C with U73122 decreased nortriptyline-induced [Ca(superscript 2+)](subscript i) rise by 75%. Taken together, nortriptyline induced [Ca(superscript 2+)](subscript i) rises in SIRC cells by causing phospholipase C-dependent Ca(superscript 2+) release from the endoplasmic reticulum and Ca(superscript 2+) influx via store-operated Ca(superscript 2+) channels.