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   <subfield code="a">Loperamide: novel effects on capacitative calcium influx</subfield>
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   <subfield code="c">[J. W. Daly, J. Harper]</subfield>
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   <subfield code="a">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.</subfield>
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   <subfield code="a">Birkhäuser Verlag Basel,, 1999</subfield>
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   <subfield code="a">Key words. Loperamide</subfield>
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   <subfield code="a">calcium channels</subfield>
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   <subfield code="u">Laboratory of Bioorganic Chemistry, Bldg 8, Rm 1A17, National Institutes of Health Bethesda (Maryland 20892, USA), Fax +1 301 402 0008, e-mail: johnd@intra.niddk.nih.gov, US</subfield>
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