Literature DB >> 2981651

Optimal conditions for measurement of Na+,K+-ATPase activity of human leucocytes.

D N Baron, F A Khan.   

Abstract

The Na+,K+-ATPase activity of human leucocytes was assayed by measuring the release of inorganic phosphate (Pi) from ATP. The maximum enzyme activity was achieved under the following conditions: concentration (mmol/l), Tris/HCl 50, Na 100, K 15, ATP 5, Mg 7, EDTA 1; pH 7.2 and temperature 37 degrees C, were optimal. Ouabain showed maximal inhibition at a concentration of 10-100 mumol/l. Ethanol, the solvent for ouabain, had a dose-related inhibitory effect. Heparin or citrate used as an anticoagulant gave similar results. Leucocyte samples could be stored at -20 degrees C for up to 6 days without loss of activity. Hypotonic lysis had advantages over sonication as the technique for cell disruption. The leucocyte Na+,K+-ATPase enzyme activity in healthy subjects was 186 mumol of Pi h-1g-1 of protein (median) with a range 136-243 mumol of Pi h-1g-1 of protein. The within-batch coefficient of variation was 6.4% and the between-batch precision was 9.6%.

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Year:  1985        PMID: 2981651     DOI: 10.1042/cs0680143

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  1 in total

1.  In vivo and in vitro sodium pump activity in subjects with thyrotoxic periodic paralysis.

Authors:  A Chan; R Shinde; C C Chow; C S Cockram; R Swaminathan
Journal:  BMJ       Date:  1991-11-02
  1 in total

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