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Psychoactivity and abuse potential of sumatriptan
J T Sullivan1, K L Preston, M P Testa
1Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Clinical Pharmacology and Therapeutics
|December 1, 1992
Summary
Sumatriptan, a migraine medication, was found to be psychoactive but has a low abuse potential. This study assessed its effects compared to morphine in individuals with a history of substance abuse.
Area of Science:
- Pharmacology
- Neuroscience
- Clinical Psychology
Background:
- Sumatriptan is a selective 5-HT1D receptor agonist used for treating migraines and cluster headaches.
- Understanding the psychoactive profile and abuse potential of therapeutic drugs is crucial for public health and safety.
Purpose of the Study:
- To evaluate the psychoactive effects and abuse liability of sumatriptan.
- To compare the subjective and physiological responses to sumatriptan with those of morphine, a known drug of abuse.
Main Methods:
- A double-blind, Latin-square crossover study involving 12 male subjects with a history of substance abuse.
- Administration of subcutaneous placebo, sumatriptan (8 and 16 mg), and morphine (10 and 20 mg).
- Assessment of subjective, behavioral, and physiological responses, including Addiction Research Center Inventory (ARCI) scales and miosis.
Main Results:
- Sumatriptan demonstrated psychoactivity and was distinguishable from placebo.
- A dose-related decrease in euphoria scores and an increase in scores for apathetic sedation and disliking were observed with sumatriptan.
- No significant changes in heart rate, blood pressure, or pupil size were noted for sumatriptan.
- Morphine produced expected dose-response effects consistent with its known reinforcing and physiological impacts.
Conclusions:
- Sumatriptan exhibits psychoactive properties but does not appear to be a prototypic drug of abuse.
- The findings suggest that sumatriptan has a low potential for abuse.
- Further research may explore the long-term implications of sumatriptan's psychoactive effects.