Paper Details 
Original Abstract of the Article :
Impulsive aggression (IA) is considered a maladaptive form of aggression that is reactive and overt and occurs outside of the acceptable social context. Many children and adolescents with attention-deficit/hyperactivity disorder (ADHD) display clinically significant aggression, with the predominant ...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254985/

データ提供:米国国立医学図書館(NLM)

SPN-810M (Molindone): A Potential New Treatment for Impulsive Aggression

Impulsive aggression (IA) is a challenging behavior that can affect children, adolescents, and adults. It's like a sudden desert storm that can erupt without warning, causing distress and disrupting relationships. This study investigates the potential therapeutic effects of SPN-810M (molindone), a drug currently used for other conditions, in the treatment of IA.

The researchers explore the pharmacological properties of SPN-810M, highlighting its potential to modulate dopamine, norepinephrine, and serotonin systems, which are implicated in impulsive aggression. This is like understanding the dynamics of sand dunes in the desert, discovering how certain factors influence their shape and movement.

A New Hope for Managing Impulsive Aggression

This study holds promise for the development of new treatments for IA, particularly in children and adolescents with attention-deficit/hyperactivity disorder (ADHD). It's like finding a new and effective way to tame the desert storms of IA, bringing peace and stability to those affected.

Dr. Camel's Conclusion

This study is like a camel caravan searching for a hidden oasis of peace in the desert of impulsive aggression. It reveals the potential of SPN-810M (molindone) as a new treatment option, offering hope for those struggling with this challenging behavior. Further research is needed to confirm its effectiveness and safety, but this discovery is a beacon of hope in the quest to manage IA.

Date :
  1. Date Completed n.d.
  2. Date Revised 2022-03-30
Further Info :

Pubmed ID

30538587

DOI: Digital Object Identifier

PMC6254985

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Languages

English

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