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5-HT2c agonist, lorcaserin, reduces aggressive responding in intermittent explosive disorder: A pilot study
1Clinical Neuroscience Research Unit, Department of Psychiatry and Behavioral Neuroscience, Pritzker School of Medicine, The University of Chicago, Chicago, Illinois.
Lorcaserin, a selective serotonin 5-HT2c agonist, reduced provoked aggressive responses in a small study. This finding suggests potential for treating impulsive aggression when other serotonin treatments fail.
Area of Science:
- Neuroscience
- Psychopharmacology
- Behavioral Science
Background:
- Impulsive aggressive behavior is linked to decreased central serotonin (5-HT) function.
- Selective serotonin reuptake inhibitors (SSRIs) are not always effective for impulsive aggression.
- Direct serotonin agonists may offer an alternative treatment approach.
Purpose of the Study:
- To evaluate the efficacy of lorcaserin, a selective 5-HT2c agonist, in reducing aggression.
- To test if lorcaserin can attenuate aggressive responding in individuals with impulsive aggression.
Main Methods:
- A randomized, placebo-controlled crossover study involving 10 adults.
- Participants received lorcaserin (20 mg) or placebo on separate days.
- Aggression was measured using the Taylor aggression paradigm.
Main Results:
- Lorcaserin significantly reduced provoked aggression compared to placebo.
- The drug decreased the frequency of administering high and extreme shock levels.
- No significant effect was observed on unprovoked aggression.
Conclusions:
- Lorcaserin demonstrates potential anti-aggressive properties in humans.
- These findings support further clinical trials for impulsive aggressive behavior treatment.
- Lorcaserin may be a viable option for individuals unresponsive to SSRIs.
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