G. Gerra et al., NALOXONE AND METERGOLINE EFFECTS ON GROWTH-HORMONE RESPONSE TO GAMMA-HYDROXYBUTYRIC ACID, International clinical psychopharmacology, 10(4), 1995, pp. 245-250
Gamma-hydroxybutyric acid (GHB) has been recently used in alcohol deto
xification, but conflicting data are available concerning the central
mechanism of action of this GABA catabolite. GHB ability to stimulate
growth hormone (GH) secretion has been reported. Our previous studies
revealed the ability of flumazenil (a benzodiazepine antagonist) to co
unteract GHB effects on GH secretion. Other hypotheses, including an o
pioid or serotonergic role of GHB, have been considered. In the presen
t study we investigated GH responses to GHB with or without naloxone (
an opiate receptor antagonist) or metergoline (a serotonin receptor an
tagonist) pretreatment. This study included 10 male healthy volunteers
(aged 24.3 +/- 2.9 years) who were submitted to four tests in random
order: (A) oral GHB administration; CB) oral GHB and i.v. naloxone adm
inistration; (C) oral GHB and oral metergoline administration; and (D)
oral placebo and i.v. saline administration. Blood samples for GH ass
ay were collected during the three tests at -15, 0, 15, 30, 45, 60 and
90 min. GHB induced a significant increase in GH plasma levels; nalox
one pretreatment did not antagonize GHB action on GH secretion; meterg
oline significantly decreased GH response to GHB (p < 0.05). No change
s were obtained with placebo and saline administration. The opioid sys
tem does not seem to be involved in GHB effects on GH-secreting pituit
ary cells; GHB effects on the serotonergic system influencing GH secre
tion, on the other hand, cannot be excluded.