Ck. Kim et al., CONTINGENT DRUG TOLERANCE - DIFFERENTIAL TOLERANCE TO THE ANTICONVULSANT, HYPOTHERMIC, AND ATAXIC EFFECTS OF ETHANOL, Pharmacology, biochemistry and behavior, 52(3), 1995, pp. 531-539
The kindled-convulsion model of epilepsy was used to study contingent
tolerance to ethanol's (1.5 g/kg; IP) anticonvulsant, hypothermic, and
ataxic effects in adult male rats. In the present experiments, three
groups of amygdala-kindled rats received a series of bidaily (one ever
y 48 h) convulsive stimulations: one group received ethanol 1 h before
each stimulation; one group received ethanol 1 h after each stimulati
on; and another group served as the saline control. Tolerance to ethan
ol's anticonvulsant effect (Experiments 1 and 2) was greatest in those
rats that received ethanol before each convulsive stimulation; wherea
s, tolerance to ethanol's hypothermic (Experiments 1 and 2) and ataxic
(Experiments 2) effects developed in both groups that received ethano
l. These results were predicted on the basis of the drug-effect theory
of drug tolerance: the theory that functional drug tolerance is an ad
aptation to the disruptive effects of drugs on concurrent patterns of
neural activity, not to drug exposure per se.