Inhibition of 5-hydroxytryptamine-mediated behaviour by the putative 5-HT2 antagonist pirenperone

Neuropharmacology. 1983 May;22(5):573-8. doi: 10.1016/0028-3908(83)90147-8.

Abstract

The effect of pirenperone, a putative 5-HT2 receptor antagonist, on various 5-HT-mediated behavioural responses has been examined. The head twitch response in mice, induced by administration of carbidopa (25 mg/kg) followed by 5-hydroxytryptophan (5-HTP) (200 mg/kg), was inhibited in a dose-dependent manner by pirenperone, with an ED50 of 76 micrograms/kg. The appearance of head weaving, forepaw treading and hind-limb abduction, which followed the administration of tranylcypromine (5 mg/kg) plus L-tryptophan (100 mg/kg) or quipazine (50 mg/kg) to rats, was also inhibited by pretreatment with pirenperone (100 micrograms/kg). Pirenperone did not alter the rate of 5-HT synthesis in the rat brain. Whilst pirenperone (100 micrograms/kg) did decrease methamphetamine-induced locomotor activity in rats, a dose of haloperidol producing a similar inhibition of this response did not alter the 5-HT-mediated behaviour. It is suggested, therefore, that the currently used 5-HT-induced behavioural models are 5-HT2 receptor-mediated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5-Hydroxytryptophan / pharmacology
  • Animals
  • Carbidopa / pharmacology
  • Haloperidol / pharmacology
  • Male
  • Methamphetamine / pharmacology
  • Motor Activity / drug effects*
  • Piperidines / pharmacology*
  • Quipazine / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Serotonin / metabolism
  • Serotonin Antagonists*
  • Tranylcypromine / pharmacology
  • Tryptophan / pharmacology

Substances

  • Piperidines
  • Serotonin Antagonists
  • Serotonin
  • Tranylcypromine
  • Methamphetamine
  • Quipazine
  • Tryptophan
  • 5-Hydroxytryptophan
  • Haloperidol
  • Carbidopa
  • pirenperone