Rb. Rosse et al., NIMODIPINE PHARMACOTHERAPEUTIC ADJUVANT THERAPY FOR INPATIENT TREATMENT OF COCAINE DEPENDENCE, Clinical neuropharmacology, 17(4), 1994, pp. 348-358
Recent preclinical studies suggest utility for voltage-sensitive calci
um channel blockers (VSCCBs) in the treatment of cocaine addiction. Th
e following double-blind placebo-controlled study examined the role of
the VSCCB nimodipine in attenuating cocaine craving in 66 recently ab
stinent cocaine-dependent patients on an inpatient substance abuse tre
atment unit utilizing an intensive 12-step milieu-oriented psychosocia
l therapy. While the medication was well tolerated, the dose of nimodi
pine used in this study (90 mg q.d.) was not superior to placebo in re
ducing background or cue-induced cocaine craving over the 3 weeks of t
he study. There was the suggestion that nimodipine might attenuate the
severity of some cocaine-induced brain deficits, as detected by evalu
ation of smooth pursuit eye movement function. A rationale for evaluat
ing higher doses of nimodipine for the treatment of cocaine addiction
is presented. As nimodipine might have anticraving and mood-stabilizin
g properties and cardio- and neuroprotective properties in the face of
cocaine intoxication and might possibly even reverse some cocaine-ind
uced brain deficits, further investigation of the role of nimodipine (
and other VSCCBs) in cocaine addiction appears an attractive avenue of
future medication development.