Mi. Rosen et al., THE EFFECT OF GAMMA-HYDROXYBUTYRIC ACID ON NALOXONE-PRECIPITATED OPIATE WITHDRAWAL, Neuropsychopharmacology, 14(3), 1996, pp. 187-193
Because gamma-hydroxybutyric acid (GHB), a GABA metabolite, attenuated
spontaneous opiate withdrawal in a prior study, we studied GHB effect
on naloxone-precipitated opiate withdrawal. Eight opiate-dependent in
patients were stabilized on the opioid levorphanol, 18 mg daily. After
an initial acclimatization challenge, subjects underwent three double
-blind challenges on consecutive days. Pretreatment in a balanced rand
omization was with either placebo, GHB, 15 mg/kg, or GHB, 30 mg/kg,fol
lowed an hour later by intravenous naloxone, 0.4 mg/70 kg. GHB produce
d no significant attenuation of multiple withdrawal measures except fo
r hot-cold feelings. GHB pretreatment slightly accelerated respiration
prior to naloxone. Differences with prior studies may be due to (1) t
iming of GHB administration (giving postwithdrawal in prior studies),
(2) direct reversal of GHB's anti-withdrawal effects by naloxone, or (
3) differences between naloxone-precipitated and spontaneous opiate wi
thdrawal.