1989•PsychobiologyOpen access

Contingent tolerance and cross-tolerance to anticonvulsant drug effects: Pentobarbital and ethanol

John P. J. Pinel, C. Kwon Kim, Dennis Paúl, Michael J. Mana

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Abstract

Tolerance to the anticonvulsant effect of pentobarbital (15 mg/kg, i.p.) was developed in amygdala-kindled rats; it was found to be contingent upon the rats’ receiving convulsive stimulations during the bidaily (once every 48 h) periods of pentobarbital exposure (Experiment 1B; contingent tolerance). Furthermore, the subjects that received convulsive stimulations while under the influence of the bidaily pentobarbital injections subsequently displayed a greater degree of cross-tolerance to the anticonvulsant effect of 1.5 g/kg of ethanol than those that had received the drug after the stimulations (Experiment 2; contingent cross-tolerance). Finally, contingent tolerance to the anticonvulsant effect of ethanol was maintained when kindled rats received convulsive stimulations during, but not before, bidaily periods of pentobarbital exposure (Experiment 3; contingent cross maintenance of tolerance). These results suggest that the repeated manifestation of particular drug effects—anticonvulsant effects in this case—play an important role in the development of some forms of drug tolerance and in their transfer to other drugs.

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Tolerance to the anticonvulsant effect of pentobarbital (15 mg/kg, i.p.) was developed in amygdala-kindled rats; it was found to be contingent upon the rats’ receiving convulsive stimulations during the bidaily (once every 48 h) periods of pentobarbital exposure (Experiment 1B; contingent tolerance). Furthermore, the subjects that received convulsive stimulations while under the influence of the bidaily pentobarbital injections subsequently displayed a greater degree of cross-tolerance to the anticonvulsant effect of 1.5 g/kg of ethanol than those that had received the drug after the stimulations (Experiment 2; contingent cross-tolerance). Finally, contingent tolerance to the anticonvulsant effect of ethanol was maintained when kindled rats received convulsive stimulations during, but not before, bidaily periods of pentobarbital exposure (Experiment 3; contingent cross maintenance of tolerance). These results suggest that the repeated manifestation of particular drug effects—anticonvulsant effects in this case—play an important role in the development of some forms of drug tolerance and in their transfer to other drugs.

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Available abstract

Tolerance to the anticonvulsant effect of pentobarbital (15 mg/kg, i.p.) was developed in amygdala-kindled rats; it was found to be contingent upon the rats’ receiving convulsive stimulations during the bidaily (once every 48 h) periods of pentobarbital exposure (Experiment 1B; contingent tolerance). Furthermore, the subjects that received convulsive stimulations while under the influence of the bidaily pentobarbital injections subsequently displayed a greater degree of cross-tolerance to the anticonvulsant effect of 1.5 g/kg of ethanol than those that had received the drug after the stimulations (Experiment 2; contingent cross-tolerance). Finally, contingent tolerance to the anticonvulsant effect of ethanol was maintained when kindled rats received convulsive stimulations during, but not before, bidaily periods of pentobarbital exposure (Experiment 3; contingent cross maintenance of tolerance). These results suggest that the repeated manifestation of particular drug effects—anticonvulsant effects in this case—play an important role in the development of some forms of drug tolerance and in their transfer to other drugs.

Key concepts: Pentobarbital, Cross-tolerance, Anticonvulsant, Drug tolerance, Pharmacology, Ethanol, Psychology, Drug

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