Gas chromatographic-mass spectrometric analysis of urinary glycyrrhetinic acid
Jazyk: | angličtina |
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Rok vydání: | 1999 |
Předmět: |
PLASMA
18 beta-glycyrrhetinic acid PERFORMANCE LIQUID-CHROMATOGRAPHY LICORICE 11-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY 11 beta-hydroxysteroid dehydrogenase HYPOKALEMIC RHABDOMYOLYSIS 18-BETA-GLYCYRRHETINIC ACID BIOLOGICAL-FLUIDS urinary gas chromatographic-mass spectrometric assay liquorice APPARENT MINERALOCORTICOID EXCESS HUMAN SERUM GLYCYRRHIZIC ACID |
Zdroj: | Journal of Internal Medicine. 246(6):539-547 |
ISSN: | 0954-6820 |
Popis: | Objectives. Liquorice abuse can lead to severe clinical complications, caused by its active compound 18 beta-glycyrrhetinic acid (18 beta GA). 18 beta GA inhibits dehydrogenase activity of 11 beta-hydroxysteroid dehydrogenase (11 beta HSD). This enzyme catalyses the interconversion between cortisol and cortisone and normally protects the mineralocorticoid receptor from being activated by cortisol. Diagnosing liquorice abuse can be notoriously difficult. The aim of our study was to develop an accurate and clinically applicable 18 beta GA urinary assay.Design. We developed a urinary 18 beta GA assay based on gas chromatography and mass spectrometry (GCMS) with sufficient sensitivity to detect 18 beta GA at low concentrations. The assay was validated in four volunteers consuming different amounts of liquorice. We applied its use in two patients with hypokalaemic hypertension and suppressed plasma renin activity and serum aldosterone, who were suspected of liquorice abuse.Results. The detection limit for 18 beta GA of the GC assay was 10 mu g L-1, which was lowered to 3 mu g L-1 by subsequent application of MS. In all volunteers, urinary 18 beta GA was detected during liquorice intake. Urinary 18 beta GA remained detectable until 5 days after stopping continued liquorice intake and until at least 51 h after ingestion of a single large amount. Urinary 18 beta GA was demonstrated in both patients, establishing a diagnosis of liquorice abuse. One patient showed changes in urinary cortisol metabolites, consistent with 11 beta HSD inhibition. Changes in cortisol metabolites were less pronounced in the other patient.Conclusion. Liquorice abuse can result in hypokalaemic hypertension with prolonged suppression of plasma renin activity and aldosterone concentration. This is caused by 18 beta GA-mediated inhibition of 11 beta HSD, resulting in activation of the renal mineralocorticoid receptor by cortisol. Urinary 18 beta GA measurement by GCMS is a useful aid in establishing liquorice abuse. |
Databáze: | OpenAIRE |
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