Liquorice ingestion attenuates vasodilatation via exogenous nitric oxide donor but not via β2-adrenoceptor stimulation

Autoři: Elina J. Hautaniemi aff001;  Antti J. Tikkakoski aff001;  Arttu Eräranta aff001;  Mika Kähönen aff001;  Esa Hämäläinen aff003;  Ursula Turpeinen aff003;  Heini Huhtala aff005;  Jukka Mustonen aff001;  Ilkka H. Pörsti aff001
Působiště autorů: Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland aff001;  Department of Clinical Physiology, Tampere University Hospital, Tampere, Finland aff002;  HUSLAB, Helsinki University Hospital, Helsinki, Finland aff003;  Department of Clinical Chemistry, Biomedicum, Helsinki University, Helsinki, Finland aff004;  Faculty of Social Sciences, Tampere University, Tampere, Finland aff005;  Department of Internal Medicine, Tampere University Hospital, Tampere, Finland aff006
Vyšlo v časopise: PLoS ONE 14(10)
Kategorie: Research Article


We examined the effect of liquorice ingestion on haemodynamic responses to exogenous nitric oxide donor (nitroglycerin) and β2-adrenoceptor agonist (salbutamol), and 11β-hydroxysteroid dehydrogenase activity, in 21 volunteers and 21 reference subjects. Haemodynamic data was captured before and after sublingual nitroglycerin (0.25 mg) and inhaled salbutamol (400 μg) during orthostatic challenge utilising radial pulse wave analysis and whole-body impedance cardiography. The recordings were performed at baseline and following two weeks of liquorice intake (290–370 mg/d glycyrrhizin). Urinary cortisone and cortisol metabolites were examined. Liquorice intake elevated aortic systolic and diastolic blood pressure and systemic vascular resistance when compared with the reference group. Following research drug administration the liquorice-induced increase in systemic vascular resistance was observed in the presence of nitroglycerin (p<0.05) but no longer in the presence of salbutamol. Liquorice ingestion decreased cardiac chronotropic response to upright posture (p = 0.032) in unadjusted analysis, but when adjusted for age and sex the difference in the upright change in heart rate was no longer significant. The urinary cortisone to cortisol metabolite ratio decreased from 0.70 to 0.31 (p<0.001) after liquorice intake indicating significant inhibition of the 11β-hydroxysteroid dehydrogenase type 2. In the reference group the haemodynamic variables remained virtually unchanged. These results suggest that liquorice exposure impaired vasodilatation in vivo that was induced by exogenous nitric oxide donor but not that induced by β2-adrenoceptor stimulation.

Trial registration: EU Clinical Trials Register 2006-002065-39 NCT01742702.

Klíčová slova:

Aldosterone – Blood plasma – Blood pressure – Cortisol – Drug research and development – Heart rate – Ingestion – Inhalation


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