Anxiolytic-like effects of NMDA/glycine-B receptor ligands are abolished during the elevated plus-maze trial 2 in rats

This publication has 41 references indexed in Scilit:

• One-trial tolerance to midazolam is due to enhancement of fear and reduction of anxiolytic-sensitive behaviors in the elevated plus-maze retest in the rat
  Pharmacology Biochemistry and Behavior, 2002
• Oxiracetam prevents the MK-801 induced amnesia for the elevated plus-maze in mice
  Behavioural Brain Research, 2000
• The phenomenon of “one-trial tolerance” to the anxiolytic effect of chlordiazepoxide in the elevated plus-maze is abolished by the introduction of a motivational conflict situation
  Life Sciences, 1999
• Effects of glycine or (±)-3-amino-l-hydroxy-2-pyrrolidone microinjections along the rostrocaudal axis of the dorsal periaqueductal gray matter on rats' performance in the elevated plus-maze task.
  Behavioral Neuroscience, 1999
• Influence of Prior Experience on Mice Behavior Using the Four-Plate Test
  Pharmacology Biochemistry and Behavior, 1997
• Anxiolytic activity of glycine-B antagonists and partial agonists—No relation to intrinsic activity in the patch clamp
  Neuropharmacology, 1997
• Effects of Ethanol, MK-801, and Chlordiazepoxide on Locomotor Activity in Different Rat Lines: Dissociation of Locomotor Stimulation from Ethanol Preference
  Alcohol, Clinical and Experimental Research, 1994
• The interplay of learning and anxiety in the elevated plus-maze
  Behavioural Brain Research, 1993
• Regulation of NMDA receptor phosphorylation by alternative splicing of the C-terminal domain
  Nature, 1993
• A Conflict Procedure Not Requiring Deprivation: Evidence That Chronic Ethanol Treatment Induces Tolerance to the Anticonflict Action of Ethanol and Chlordiazepoxide
  Alcohol, Clinical and Experimental Research, 1989