Our objective was to assess thermogenic action of fluoxetine (FL) in obese
menopausal women, evaluating the effect of FL administration on resting ene
rgy expenditure (REE) and on glucose-induced thermogenesis both after acute
administration (40 mg in single dose the evening before measurements) and
after a 12- week period of diet treatment plus FL (60 mg per day) or placeb
o. It was a double-blind, placebo-controlled design both in acute and in ch
ronic study. The subjects were 32 obese, otherwise healthy, menopausal wome
n. The patients were assigned randomly to three groups, one performing an a
cute study protocol, in which resting and glucose-induced thermogenesis was
measured after FL and placebo administration, performed in randomised orde
r. The other two groups underwent dietary plus pharmacological treatment (F
L or placebo, FL). Resting and glucose-induced thermogenesis was measured a
t baseline and after 12 weeks of treatment. The results showed that acute F
L administration caused an increase in resting energy expenditure (PL: 5.35
+/-0.18 vs FL: 5.53+/-0.24 KJ/min, p<0.05). A significant decrease of REE w
as observed in the PL group after 12 weeks (p<0.03), while a slight, but no
t significant, decrease was observed in the FL group (p=NS). FL did not aff
ect thermic response to oral glucose neither after acute nor chronic admini
stration (p=NS for all groups studied). The conclusion was that our data gi
ve support to thermogenic actions of FL after acute administration, suggest
ing also that chronic FL treatment may restrain to some degree the metaboli
c adaptation expected during weight loss in obese subjects. At variance wit
h what observed with other drugs, such as dexfenfluramine, an increased the
rmic effect of oral glucose does not seem to be involved in the thermogenet
ic action of FL. (C) 2000, Editrice Kurtis.