Radioimmunoassay of endothelin in human plasma

Peter Have Rasmussen*, Inger Graves Plum, Niels Eske Bruun, Harriet Dige-Petersen, Thomas Hedner, Jan Hedner, Jørn Giese

*Corresponding author af dette arbejde

    Publikation: Bidrag til tidsskriftArtikelForskningpeer review


    A specific and sensitive radioimmunoassay (RIA) for determination of endothelin-1 (ET-1) in human plasma has been developed. Antibodies were raised in rabbits using synthetic ET-1 conjugated to thyroglobulin as immunogen. The antibodies obtained were used at a final dilution of 1:300,000 yielding maximum binding of 61.7 ± 3.0% (mean ± 1 SD, n = 20) of 125I-ET-I. The ID50 (inhibitory dose 50% was 4.5 ± 0.6 fmol/100 μl (mean ± 1 SD, n = 20). The sensitivity of the RIA was 0.33 fmol/100 μl standard solution. No cross reactivity was observed with endothelin-3, big-endothelin-1, atrial natriuretic factor, angiotensin 1 or angiotensin II. The cross-reactivity with endothelin-2 was 100% Endothelin was extracted from acidified plasma with Sep-pak C18 cartridges and recovery of ET-1 added to normal plasma was 70.9 ± 10.3% (mean ± 1 SD, n = 12). The concentration of ET-1 in plasma from normal subjects was 1.5 ± 0.4 pmol/l (mean ± SD, n = 11) ranging from 1.0 to 2.2 pmol/1. Extracts of normal human plasma subjected to high performance liquid chromatography on a reverse phase C18 column showed one peak of immunoreactivity co-eluting with the standard for ET-1. From these data it is concluded that the immunoreactive material measured in normal plasma with the present RIA is identical to ET-1.

    Sider (fra-til)181-186
    Antal sider6
    TidsskriftBlood Pressure
    Udgave nummer3
    StatusUdgivet - 1 jan. 1992


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