Role of 5-HT 2A and 5-HT 2C Receptor Subtypes in the Two Types of Fear Generated by the Elevated T-Maze

Role of 5-HT 2A and 5-HT 2C Receptor Subtypes in the Two Types of Fear Generated by the Elevated... To study the role of 5-HT 2A and 5-HT 2C receptor subtypes in anxiety, the behavioral effects of drugs that either block or stimulate these receptors were measured in an animal model of anxiety, the elevated T-maze. One arm of the maze is enclosed by walls and stands perpendicular to the two open arms. Inhibitory (passive) avoidance—representing learned fear—was measured by placing a rat at the end of the enclosed arm and recording the time to leave this arm with the four paws during three consecutive trials. After 30 s, the same animal was placed at the end of one of the open arms and the time to leave this arm with the four paws was recorded. This one-way escape response represents unconditioned fear. The IP injection of the preferential 5-HT 2C receptor agonists mCPP and TFMPP (0.1–0.8 mg/kg), 25 min before the experimental session enhanced inhibitory avoidance. In contrast, the same drugs either tended to impair (mCPP) or significantly inhibited (TFMPP) one-way escape. The preferential 5-HT 2A agonist DOI (0.03–0.3 mg/kg) did not change either inhibitory avoidance or one-way escape. Inhibitory avoidance was impaired by the selective 5-HT 2C antagonists SB 200646A (3.0–30 mg/kg) and SDZ SER 082 (0.1–1.0 mg/kg), by the 5-HT 2A antagonist SR 46349B (1.0–10.0 mg/kg), and by the mixed 5-HT 2A/2C antagonist ritanserin (0.3–3.0 mg/kg). However, it was not affected by the selective 5-HT 2A antagonist RP 62203 (0.25–4.0 mg/kg). All the 5-HT 2 antagonists used were ineffective on one-way escape. Therefore, conditioned fear seems to be tonically facilitated through 5-HT 2C receptor stimulation, although the 5-HT 2A receptor may also participate in its regulation. Unconditioned fear might be phasically inhibited by 5-HT 2C receptor activation. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Pharmacology Biochemistry and Behavior Elsevier

Role of 5-HT 2A and 5-HT 2C Receptor Subtypes in the Two Types of Fear Generated by the Elevated T-Maze

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Publisher
Elsevier
Copyright
Copyright © 1997 Elsevier Science Inc.
ISSN
0091-3057
eISSN
1873-5177
DOI
10.1016/S0091-3057(97)00057-9
Publisher site
See Article on Publisher Site

Abstract

To study the role of 5-HT 2A and 5-HT 2C receptor subtypes in anxiety, the behavioral effects of drugs that either block or stimulate these receptors were measured in an animal model of anxiety, the elevated T-maze. One arm of the maze is enclosed by walls and stands perpendicular to the two open arms. Inhibitory (passive) avoidance—representing learned fear—was measured by placing a rat at the end of the enclosed arm and recording the time to leave this arm with the four paws during three consecutive trials. After 30 s, the same animal was placed at the end of one of the open arms and the time to leave this arm with the four paws was recorded. This one-way escape response represents unconditioned fear. The IP injection of the preferential 5-HT 2C receptor agonists mCPP and TFMPP (0.1–0.8 mg/kg), 25 min before the experimental session enhanced inhibitory avoidance. In contrast, the same drugs either tended to impair (mCPP) or significantly inhibited (TFMPP) one-way escape. The preferential 5-HT 2A agonist DOI (0.03–0.3 mg/kg) did not change either inhibitory avoidance or one-way escape. Inhibitory avoidance was impaired by the selective 5-HT 2C antagonists SB 200646A (3.0–30 mg/kg) and SDZ SER 082 (0.1–1.0 mg/kg), by the 5-HT 2A antagonist SR 46349B (1.0–10.0 mg/kg), and by the mixed 5-HT 2A/2C antagonist ritanserin (0.3–3.0 mg/kg). However, it was not affected by the selective 5-HT 2A antagonist RP 62203 (0.25–4.0 mg/kg). All the 5-HT 2 antagonists used were ineffective on one-way escape. Therefore, conditioned fear seems to be tonically facilitated through 5-HT 2C receptor stimulation, although the 5-HT 2A receptor may also participate in its regulation. Unconditioned fear might be phasically inhibited by 5-HT 2C receptor activation.

Journal

Pharmacology Biochemistry and BehaviorElsevier

Published: Dec 1, 1997

References

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