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Cellular and Molecular Life Sciences: CMLS logoLink to Cellular and Molecular Life Sciences: CMLS
. 2000 Jan;57(1):149–157. doi: 10.1007/s000180050504

Loperamide: novel effects on capacitative calcium influx

J W Daly 1, J Harper 1
PMCID: PMC11146794  PMID: 10949586

Abstract.

Loperamide is a widely used antidiarrheal that primarily acts at nanomolar concentrations through activation of opioid receptors in the gastrointestinal tract. At somewhat higher concentrations, loperamide blocks calmodulin activity, calcium channels, N-methyl-d-aspartate-receptor channels, and maitotoxin-elicited calcium influx. Loperamide at micromolar concentrations has now been shown to have a remarkable stimulatory effect on the capacitative calcium influx that is triggered in many cells by depletion of the inositol-trisphosphate-sensitive stores of calcium in the endoplasmic reticulum. The mechanism whereby loperamide enhances levels of intracellular calcium elevated by capacitative calcium influx is, as yet, undefined.

Keywords: Key words. Loperamide; calcium channels; calcium stores; maitotoxin; inositol trisphosphate; thapsigargin; ATP.

Footnotes

Received 22 July 1999; received after revision 17 September 1999; accepted 5 October 1999


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