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Studies on the Permeability of the Intervertebral Disc During Skeletal Maturation
ASKFOOD, a knowledge alliance between businesses and academia in the food-related sectors to leverage innovation and sustainability
ASKFOOD, a knowledge alliance between businesses and academia in the food-related sectors to leverage innovation and sustainability/Pittia, P.; Di Falco, G.; Schleining, G.; Tsaltas, D.; Drausinger, J.; Verker, R.; Biesdorf, B.; Medic, H.; Lazaro-Mojica, J.; Sabbatini, G.; Salta, F..-ELETTRONICO.-(2020).((Intervento presentato al convegno 34th EFFoST International Conference Bridging high-tech, food-tech and health: Consumer-oriented innovations
Reinforced spatial alternation as an animal model of obsessive-compulsive disorder (OCD): Investigation of 5-HT2C and 5-HT1D receptor involvement in OCD pathophysiology
Background: This study introduces a laboratory model of compulsive
behavior based on persistence in the context of rewarded spatial
alternation.
Methods. Rats were screened for spontaneous persistence during T-maze
reinforced alternation. Experiment 1: One high and one low spontaneous
persistence group (n = 8) received 20 injections of fluoxetine, a
matched pair saline, both followed by 4 days of
meta-chloropbenylpiperazine (mCPP) challenge. Experiment 2.. Five
matched groups of rats (n = 9) received pretreatment (20 injections)
with fluoxetine, mCPP, desipramine, diazepam or saline, followed by 4
days of mCPP challenge (fluoxetine in mCPP group). After washout,
animals received 2 days of naratriptan, followed by another 2-day mCPP
challenge.
Results: In both experiments mCPP significantly increased persistence in
saline controls. Fluoxetine also acutely increased persistence scores:
after a gradual return to baseline, these scores showed tolerance to
mCPP. Experiment 1: This pattern was significant in high but not low
initial persistence groups. Experiment 2: Fluoxetine and mCPP showed
cross-tolerance. Neither desipramine nor diazepam protected against mCPP
challenge. Persistence scores returned to baseline during washout and
naratriptan and were thereafter increased by another mCPP challenge in
all but the fluoxetine and mCPP groups, suggesting 5-HT2c receptor
mediation.
Conclusions. This model is based on spontaneous persistence behavior
showing pharmacological responses concordant with those of compulsive
symptomatology