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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Psychopharmacologyarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Psychopharmacology
Article . 1972 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
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Tolerance and cross-tolerance to mescaline and amphetamine as a function of central and peripheral administration

Authors: S B, Sparber; H A, Tilson;

Tolerance and cross-tolerance to mescaline and amphetamine as a function of central and peripheral administration

Abstract

Differences in tolerance and cross-tolerance to the behavioral effects of d-amphetamine sulfate and mescaline hydrochloride were studied as a function of intraventricular or intraperitoneal routes of administration. Operant behavior, using a fixed ratio schedule of food reinforcement, was the behavioral variable. Following tolerance to d-amphetamine infused intraventricularly, an approximately equipotent dose of mescaline, similarly administered the next day, resulted in behavioral disruption indicating a lack of cross-tolerance. However, following tolerance to mescaline administered intraventricularly, an equipotent dose of d-amphetamine infused the next day did not result in behavioral disruption, indicating cross-tolerance, When d-amphetamine (1.6 or 2.5 mg/kg) and mescaline (10 mg/kg) were administered peripherally (i.p.), no cross-tolerance was found, regardless of the order of drug presentation. Finally, tolerance to amphetamine administered intraventricularly was not indicative of tolerance to amphetamine given intraperitoneally. The next day (after central tolerance) amphetamine disrupted the operant to an equal or greater extent than it had prior to central tolerance formation. This is further evidence that drugs administered directly into the CNS may not be producing their behavioral effects in the same manner as they do via peripheral administration.

Related Organizations
Keywords

Male, Mescaline, Dextroamphetamine, Reinforcement Schedule, Behavior, Animal, Rats, Inbred Strains, Drug Tolerance, Cerebral Ventricles, Rats, Animals, Drug Interactions, Food Deprivation, Injections, Intraperitoneal, Injections, Spinal

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    popularity
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    influence
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
26
Average
Top 10%
Top 10%
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