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Classics in Chemical Neuroscience: Dextromethorphan (DXM)
Elliot W McClure1, R Nathan Daniels2
1Department of Pharmaceutical Sciences, Lipscomb University College of Pharmacy, Nashville, Tennessee 37204, United States.
Dextromethorphan (DXM), a non-opioid cough suppressant, also exhibits psychedelic effects at high doses due to N-methyl-d-aspartate receptor antagonism. This review explores its multifaceted profile in chemical neuroscience.
Area of Science:
- Chemical Neuroscience
- Pharmacology
- Psychiatry
Background:
- Dextromethorphan (DXM) is a widely used, non-opioid cough suppressant introduced in 1958.
- It is also indicated for various psychiatric disorders.
- High doses of DXM produce intoxicating and psychedelic effects, similar to dissociative anesthetics.
Purpose of the Study:
- To provide a comprehensive review of Dextromethorphan (DXM).
- To discuss its synthesis, pharmacology, metabolism, and therapeutic importance.
- To highlight its role in chemical neuroscience.
Main Methods:
- Literature review of Dextromethorphan (DXM).
- Analysis of pharmacological mechanisms, including N-methyl-d-aspartate receptor (NMDAr) antagonism.
- Examination of historical data, therapeutic uses, and recreational abuse potential.
Main Results:
- DXM's efficacy in cough suppression is linked to NMDAr antagonism.
- Supratherapeutic doses of DXM exhibit properties of dissociative hallucinogens.
- DXM possesses a complex pharmacological profile with therapeutic and psychoactive effects.
Conclusions:
- Dextromethorphan (DXM) is a versatile compound with significant therapeutic applications and psychoactive properties.
- Its mechanism of action at NMDAr receptors underpins both its medicinal and recreational effects.
- DXM represents a classic example in chemical neuroscience due to its diverse actions.
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