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. 1991 Jan;48(1):7-12.
doi: 10.1007/BF02555790.

Inhibitor action on placental calcium transport

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Inhibitor action on placental calcium transport

J M Williams et al. Calcif Tissue Int. 1991 Jan.

Abstract

Human term placental lobules were dually perfused with Krebs Ringer solution at 37 degrees C under open circuit conditions. Provided that perfusate Ca2+ concentrations were between 2.33 and 2.55 mM, there was a steady release of Ca2+ into the fetal circulation and uptake of Ca2+ from the maternal circulation. There was no significant calcium (Ca) protein binding in the perfusates. Addition of dinitrophenol altered the release of Ca2+ to an uptake on the fetal circuit and enhanced Ca2+ uptake on the maternal circuit. It also produced a release of potassium (K)+ and an uptake of Na+ on both sides of the placenta. Ouabain had no significant effect on Ca movements although it produced a marked release of K+ into the fetal perfusate. The effect of cooling on the fetal circuit was similar to that of dinitrophenol (DNP), although it did not produce significant changes in either Ca2+ or K+ movements on the maternal side of the lobule. Both DNP and cooling reduced the Ca concentration ratio between fetal and maternal outflows to unity. Replacement of Na+ by choline Ringer had only transient effect on the extraction of 45Ca from fetal perfusate. These observations indicate that a Ca2+/Na (sodium)+ exchanger does not make a major contribution to the transplacental movement of Ca2+ from mother to fetus and that this process is more probably associated with membrane-bound ATPases.

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References

    1. J Dev Physiol. 1986 Dec;8(6):435-45 - PubMed
    1. Am J Physiol. 1970 Aug;219(2):540-5 - PubMed
    1. Placenta. 1984 Jul-Aug;5(4):281-92 - PubMed
    1. Biochim Biophys Acta. 1975 Aug 20;401(2):256-64 - PubMed
    1. Am J Physiol. 1987 Jan;252(1 Pt 1):C38-46 - PubMed

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