The effects of amlodipine (from 0.1 to 3.0 mg/kg) on rats' pressing for rew
arding brain stimulation, with and without cocaine administration, were ass
essed. None of the doses reliably modified the effects of cocaine. Also, am
lodipine was given to two groups of rats taking alcohol: one group that was
regularly taking a sweetened alcoholic beverage and the ether taking an un
sweetened alcoholic beverage. The only discernible effects of amlodipine on
alcohol intake were associated with the highest dose and only with rats ta
king the sweetened beverage. The effects of this high dose could easily be
attributable to behavioral toxicity elicited by the dose. In contrast, and
confirming previous work, isradipine, another calcium channel inhibitor, pr
oduced reliable reductions on both cocaine's and alcohol's reinforcing effe
cts. Despite the similarity of isradipine and amlodipine, isradipine appare
ntly has some unique features with respect to cocaine and alcohol. (C) 1999
Elsevier Science Inc.