Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1976 Dec 21;51(1):9-14.
doi: 10.1007/BF00426314.

Inhibition of conditional avoidance response by neuroleptics upon repeated administration

Inhibition of conditional avoidance response by neuroleptics upon repeated administration

P Danneskiold-Samsøoe et al. Psychopharmacology (Berl). .

Abstract

Development of tolerance to neuroleptic compounds tested in the conditional avoidance model was investigated. Since tolerance may manifest itself by a diminished potency and/or a shortened duration of effect, the complete time course of effect was registered in these experiments. Rats were pretreated approximately 2 weeks with daily oral doses of chlorprothixene (20 mg/kg), flupenthixol (10 mg/kg), fluphenazine (2.5 mg/kg), or haloperidol (10 mg/kg) or twice a week with piflutixol (0.31 mg/kg). Three days after withdrawal chlorprothixene and flupenthixon caused a slightly but significantly weaker inhibition of avoidance performance in rats pretreated with the respective compounds and compared with non-pretreated rats, the duration of effect was shortened. Six dasy after withdrawal of piflutixol the duration of effect of a dose of piflutixol causing maximum inhibition was significantly shortened, while no homologous tolerance could be demonstrated in fluphenazine-pretreated rats. Cross tolerance was found after haloperidol-pretreatment when the rats were tested with fluphenazine 6 days after withdrawal. Homologous piflutixol tolerance could be shown 4 weeks after withdrawal. These results indicate that it is possible to demonstrate a slight tolerance to the effect of neuroleptic compounds when these are tested in conditional avoidance experiments. The cause of this tolerance is discussed.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Arzneimittelforschung. 1974 Sep;24(9):1292-4 - PubMed
    1. J Neurochem. 1975 Nov;25(5):681-6 - PubMed
    1. Psychopharmacologia. 1974 Jan 11;34(2):105-9 - PubMed
    1. Eur J Pharmacol. 1973 Jun;22(3):287-94 - PubMed
    1. Acta Physiol Scand Suppl. 1971;367:69-93 - PubMed

Substances

LinkOut - more resources