The widespread combined use of alcohol and cocaine across the United States
underscores the importance of understanding how the actions of those two a
gents interact upon important physiological regulatory processes. In an exp
eriment exploring acute ethanol-cocaine interactions, 16 rats were given 2.
0 g/kg (IP) doses of ethanol at time zero. Two hours later, half of the rat
s were given cocaine (20 mg/kg, IP), while the other half were given inject
ions of saline. The group given cocaine displayed a prolongation of the hyp
othermia condition induced by ethanol injection. In a chronic experiment, t
hree groups of rats (n = 6-8) were exposed for an 11-day period to daily IP
injections of 10 mg/kg cocaine, 20 mg/kg of cocaine, or saline. On day 12
these groups did not differ in their response to loss of the righting refle
x induced by a 3.0 g/kg dose of ethanol. However, recovery from ethanol hyp
othermia was more rapid in the rats exposed to chronic cocaine. In summary,
these initial studies provide evidence for exacerbation of the acute hypot
hermic effects of ethanol when a cocaine challenge is given 2 h after ethan
ol. In contrast, ethanol hypothermia was observed to be reduced when tested
on day 12 after an Ii-day chronic regimen of cocaine. Other dosage regimen
s and response measures need to be tested to understand the full scope of a
cute and chronic cocaine-ethanol interactions and the possible health conse
quences. (C) 1998 Elsevier Science Inc.