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Esketamine: Difference between revisions

From Pharmacopedia
[checked revision][pending revision]
Expand Esketamine with Stahl-sourced detail (with skepticism)
Sentence-case category link per house style (NMDA_Receptor_Antagonists → NMDA_receptor_antagonists)
 
(One intermediate revision by one other user not shown)
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| pregnancy      = Avoid; may cause fetal harm
| pregnancy      = Avoid; may cause fetal harm
| legal          = Rx, Schedule III (US). REMS program required.
| legal          = Rx, Schedule III (US). REMS program required.
| intro          = '''Esketamine''' (brand name Spravato) is the S-enantiomer of ketamine, FDA-approved as an intranasal medication for treatment-resistant depression (March 2019) and for major depression with acute suicidal ideation or behavior (August 2020). The S-enantiomer has approximately 4-fold higher NMDA receptor affinity than the R-enantiomer; Spravato delivers it via a nasal spray under direct medical supervision in a REMS-certified setting due to risks of dissociation, sedation, and abuse.
| intro          = '''Esketamine''' (brand name Spravato) is the S-enantiomer of ketamine, FDA-approved as an intranasal medicine for treatment-resistant depression (March 2019) and for major depression with acute suicidal ideation or behavior (August 2020). The S-enantiomer has approximately 4-fold higher NMDA receptor affinity than the R-enantiomer; Spravato delivers it via a nasal spray under direct medical supervision in a REMS-certified setting due to risks of dissociation, sedation, and abuse.


Mechanism: uncompetitive NMDA receptor antagonism on GABA interneurons disinhibits glutamatergic output, leading to AMPA receptor activation, BDNF/VEGF release, and rapid synaptogenesis through mTOR pathway activation. Antidepressant onset within hours is striking compared to monoaminergic antidepressants (4-6 weeks). Patients must be monitored ≥2 hours after dose due to dissociation, sedation, and blood pressure elevation.
Mechanism: uncompetitive NMDA receptor antagonism on GABA interneurons disinhibits glutamatergic output, leading to AMPA receptor activation, BDNF/VEGF release, and rapid synaptogenesis through mTOR pathway activation. Antidepressant onset within hours is striking compared to monoaminergic antidepressants (4-6 weeks). Patients must be monitored ≥2 hours after dose due to dissociation, sedation, and blood pressure elevation.
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[[Category:Dissociative Anesthetics]]
[[Category:Dissociative Anesthetics]]
[[Category:General (IV) Anesthetics]]
[[Category:General (IV) Anesthetics]]
[[Category:NMDA Receptor Antagonists]]
[[Category:NMDA receptor antagonists]]
[[Category:Antidepressants]]
[[Category:Antidepressants]]
[[Category:Dissociatives]]
[[Category:Dissociatives]]