, Volume 93, Issue 4, pp 502–506

Effects in the X-maze anxiety model of agents acting at 5-HT1 and 5-HT2 receptors

  • M. A. E. Critchley
  • S. L. Handley
Original Investigations

DOI: 10.1007/BF00207243

Cite this article as:
Critchley, M.A.E. & Handley, S.L. Psychopharmacology (1987) 93: 502. doi:10.1007/BF00207243


Three 5-HT agonists produced a dose-related fall in open/total arm entry ratio in the elevated X-maze model of anxiety at doses which did not affect total entries. The relative potency, 8-hydroxy-2-(di-n-propylamino)tetra lin (8-OH-DPAT)≫5-methoxy-N,N-dimethyltryptamine (5-MeODMT)>=5-methoxy-3(tetrahydropyridin-4-yl)1H-indole (RU 24969), was unrelated to the occurrence of wet dog shakes and suggests that 5-HT1 rather than 5-HT2 receptors may be involved. However, the 5-HT2 receptor antagonists ritanserin, ketanserin and seganserin caused an anxiolytic-like increase in entry ratio, although only ritanserin produced this effect across the dose range tested. +/-Pindolol, an antagonist at 5-HT1 receptors, showed a biphasic dose-response curve with a fall in entry ratio at one high dose. The effect of a submaximal dose of 8-OH-DPAT was prevented by pindolol but not by a similarly anxiolytic dose of ritanserin or diazepam. A higher dose of diazepam caused intense muscle hypotonia in combination with 8-OH-DPAT. Since open/total entry ratio appears to represent choice, rather than suppression or delay, of a response, the effects seen may indicate involvement of 5-HT receptors in anxiety separately from any change in the ability to withhold a response. The precise role of each receptor subtype, however, remains to be determined.

Key words

X-mazeAnxiety5-HT ligands

Copyright information

© Springer-Verlag 1987

Authors and Affiliations

  • M. A. E. Critchley
    • 1
  • S. L. Handley
    • 1
  1. 1.Drug Mechanisms Research Group, Pharmaceutical Sciences InstituteAston UniversityBirminghamUK