Licorice can induce a hypermineralocorticoid syndrome. Current literat
ure usually refers to the effects of sweets containing glycyrrhizin, b
ut little is known about the consequences of a prolonged intake of ''p
ure licorice''. We administered graded daily doses of dried, aqueous e
xtract of licorice root, containing 108, 217, 380 and 814 mg of glycyr
rhizin, to 4 groups of 6 healthy volunteers of both sexes for 4 weeks.
No significant effects occurred in groups 1 and 2. After 2 weeks, sid
e effects leading to withdrawal from the protocol occurred in a female
in group 3 (headache), a male with a family history of hypertension i
n group 4 (arterial hypertension), and a female also taking oral contr
aceptives in group 4 (hypertension, hypokalaemia and peripheral edema)
. In group 4, transient reduction in kalaemia and increase in body wei
ght were found after 1 and 2 weeks, respectively. A depression of plas
ma renin activity occurred in groups 3 and 4. In healthy subjects, onl
y the highest doses of licorice led to untoward effects. These were fa
voured by subclinical disease or oral contraceptives, and were less co
mmon and pronounced than what has been reported after the intake of gl
ycyrrhizin taken as such or as a flavouring agent in confectionery pro
ducts.