MGlu5 antagonism impairs exploration and memory of spatial and non-spatial stimuli in rats

Metabotropic glutamate receptor subtype 5 (mGlu5) has been implicated in memory processing in some but not all learning tasks. The reason why this receptor is involved in some tasks but not in others remains to be determined. The present experiments using rats examined effects of the mGlu5-antagonis...

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Veröffentlicht in:Behavioural brain research 2008-08, Vol.191 (2), p.235-245
Hauptverfasser: Christoffersen, Gert R.J., Simonyi, Agnes, Schachtman, Todd R., Clausen, Bettina, Clement, David, Bjerre, Vicky K., Mark, Louise T., Reinholdt, Mette, Schmith-Rasmussen, Kati, Zink, Lena V.B.
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container_end_page 245
container_issue 2
container_start_page 235
container_title Behavioural brain research
container_volume 191
creator Christoffersen, Gert R.J.
Simonyi, Agnes
Schachtman, Todd R.
Clausen, Bettina
Clement, David
Bjerre, Vicky K.
Mark, Louise T.
Reinholdt, Mette
Schmith-Rasmussen, Kati
Zink, Lena V.B.
description Metabotropic glutamate receptor subtype 5 (mGlu5) has been implicated in memory processing in some but not all learning tasks. The reason why this receptor is involved in some tasks but not in others remains to be determined. The present experiments using rats examined effects of the mGlu5-antagonist 2-methyl-6-(phenylethynyl)-pyridine (MPEP) – applied systemically i.p. (1–10mg/kg) or bilaterally into the prelimbic cortex (1–10μg) – on the ability of rats to explore and remember new stimuli. A cross-maze, open field, and object recognition task were used to evaluate exploration and memory and it was found that: (1) locomotion during exploration of spatial environments and exploration time at novel objects were reduced by i.p. but not by prelimbic administration of MPEP, (2) spatial short-term memory was impaired in cross-maze and object discrimination was reduced after both types of administration, (3) long-term retention of spatial conditioning in the cross-maze was inhibited after i.p. applications which (4) also inhibited spontaneous alternation performance during maze-exploration. Reduced exploratory locomotion and exploration time after i.p. injections may have contributed to the observed retention impairments. However, the fact that prelimbic administration of MPEP inhibited retention without reducing exploration shows that memory formation was also impacted directly by prelimbic mGlu5 in both spatial and non-spatial learning.
doi_str_mv 10.1016/j.bbr.2008.03.032
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subjects Analysis of Variance
Animals
Antagonist
Behavior, Animal - drug effects
Behavioral psychophysiology
Biological and medical sciences
Cerebral Cortex - drug effects
Dose-Response Relationship, Drug
Drug Administration Routes
Excitatory Amino Acid Antagonists - administration & dosage
Exploration
Exploratory Behavior - drug effects
Fundamental and applied biological sciences. Psychology
GABA Antagonists - administration & dosage
Locomotion - drug effects
Male
Maze learning
Maze Learning - drug effects
Memory Disorders - chemically induced
mGlu5 receptor
MPEP
Object recognition
Pattern Recognition, Physiological - drug effects
Picrotoxin - administration & dosage
Prelimbic cortex
Psychology. Psychoanalysis. Psychiatry
Psychology. Psychophysiology
Pyridines - administration & dosage
Rat
Rats
Rats, Sprague-Dawley
Space Perception - drug effects
Time Factors
title MGlu5 antagonism impairs exploration and memory of spatial and non-spatial stimuli in rats
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