Bromocriptine, dihydroergotoxine and sleep in rats: effects of repeated administration

Gerontology. 1981;27(3):152-7. doi: 10.1159/000212464.

Abstract

Bromocriptine mesylate (7.5 mg/kg, i.p.) and dihydroergotoxine mesylate (DHET); 3 mg/kg, i.p.) were administered 4 times at 9-hour intervals within a 27-hour period to rats polygraphically recorded for 84 h. Administration of bromocriptine resulted in increased wakefulness and reduced slow-wave sleep (SWS) and rapid eye movement sleep (REM) during the 0- to 36-hour period. Reduction of SWS or REM during this time period was not followed by a rebound of SWS or REM during the next 36- to 84-hour period. In addition, there was a significant reduction of SWS during the entire 0- to 84-hour period. Administration of DHET to rats did not significantly affect sleep although there was a tendency for wakefulness to increase and for SWS and REM to decrease. It appears that the effects of repeated administration of the two ergot compounds on the sleep-wakefulness cycle in rats may be indicative of the drugs' role in fulfillment of sleep 'need'.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bromocriptine / administration & dosage*
  • Bromocriptine / pharmacology
  • Dihydroergotoxine / administration & dosage*
  • Dihydroergotoxine / pharmacology
  • Male
  • Rats
  • Receptors, Dopamine / drug effects
  • Sleep / drug effects*
  • Wakefulness / drug effects

Substances

  • Receptors, Dopamine
  • Dihydroergotoxine
  • Bromocriptine