Literature DB >> 29248945

(±)-MDMA and its enantiomers: potential therapeutic advantages of R(-)-MDMA.

Elizabeth G Pitts1, Daniel W Curry1,2, Karly N Hampshire1, Matthew B Young1, Leonard L Howell3,4.   

Abstract

The use of (±)-3,4-methylenedioxymethamphetamine ((±)-MDMA) as an adjunct to psychotherapy in the treatment of psychiatric and behavioral disorders dates back over 50 years. Only in recent years have controlled and peer-reviewed preclinical and clinical studies lent support to (±)-MDMA's hypothesized clinical utility. However, the clinical utility of (±)-MDMA is potentially mitigated by a range of demonstrated adverse effects. One potential solution could lie in the individual S(+) and R(-) enantiomers that comprise (±)-MDMA. Individual enantiomers of racemic compounds have been employed in psychiatry to improve a drug's therapeutic index. Although no research has explored the individual effects of either S(+)-MDMA or R(-)-MDMA in humans in a controlled manner, preclinical research has examined similarities and differences between the two molecules and the racemic compound. This review addresses information related to the pharmacodynamics, neurotoxicity, physiological effects, and behavioral effects of S(+)-MDMA and R(-)-MDMA that might guide preclinical and clinical research. The current preclinical evidence suggests that R(-)-MDMA may provide an improved therapeutic index, maintaining the therapeutic effects of (±)-MDMA with a reduced side effect profile, and that future investigations should investigate the therapeutic potential of R(-)-MDMA.

Entities:  

Keywords:  Enantiomer; Isomer; MDMA; R(−)-MDMA; Therapeutic

Mesh:

Substances:

Year:  2017        PMID: 29248945     DOI: 10.1007/s00213-017-4812-5

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  131 in total

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Authors:  M Hiramatsu; A K Cho
Journal:  Neuropharmacology       Date:  1990-03       Impact factor: 5.250

4.  Acute prosocial effects of oxytocin and vasopressin when given alone or in combination with 3,4-methylenedioxymethamphetamine in rats: involvement of the V1A receptor.

Authors:  Linnet Ramos; Callum Hicks; Richard Kevin; Alex Caminer; Rajeshwar Narlawar; Michael Kassiou; Iain S McGregor
Journal:  Neuropsychopharmacology       Date:  2013-05-16       Impact factor: 7.853

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Authors:  Michael C Mithoefer; Charles S Grob; Timothy D Brewerton
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Journal:  Eur J Neurosci       Date:  2007-11-14       Impact factor: 3.386

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Journal:  Biochem Pharmacol       Date:  1987-07-15       Impact factor: 5.858

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Journal:  Brain Res       Date:  1992-11-06       Impact factor: 3.252

9.  Microglial and astroglial activation by 3,4-methylenedioxymethamphetamine (MDMA) in mice depends on S(+) enantiomer and is associated with an increase in body temperature and motility.

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Journal:  J Neurochem       Date:  2012-11-15       Impact factor: 5.372

10.  3,4-Methylenedioxymethamphetamine facilitates fear extinction learning.

Authors:  M B Young; R Andero; K J Ressler; L L Howell
Journal:  Transl Psychiatry       Date:  2015-09-15       Impact factor: 6.222

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3.  Acute effects of 3,4-methylenedioxymethamphetamine (MDMA) and R(-) MDMA on actigraphy-based daytime activity and sleep parameters in rhesus monkeys.

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Review 4.  DARK Classics in Chemical Neuroscience: Aminorex Analogues.

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Review 5.  MDMA and memory, addiction, and depression: dose-effect analysis.

Authors:  Madeline M Pantoni; Jinah L Kim; Kaitlin R Van Alstyne; Stephan G Anagnostaras
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  5 in total

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