Robust and rapid antidepressant effects resulted from a single intravenous dose of an N-methyl-D-aspartate antagonist; onset occurred within 2 hours postinfusion and continued to remain significant for 1 week.â€ś
To our knowledge, there has never been a report of any other drug or somatic treatment (ie, sleep deprivation, thyrotropin-releasing hormone, antidepressant, dexamethasone, or electroconvulsive therapy) that results in such a dramatic rapid and prolonged response with a single administration.â€ť
The mechanism of its action, however, is still unknown.
A new (2017) study, covered in Nature suggests that a previous theory (that it inhibits the brain's NMDA-receptors) may be incorrect.
Their finding adds to recent studies contradicting a long-held idea that the drug works mainly by blocking proteins called NMDA receptors, on the surface of brain cells, which transmit signals between those cells.â€ś
A third (also as yet unproven) theory instead suggests that breakdown chemicals of the drug - rather than the drug itself - may be responsible for its anti-depressant effects.
Note: The 'enantiomer' (i.e. mirror image molecule) of Ketamine is called Esketamine (marketed under the name Ketanest and others) it has similar properties, and is also used to treat depression - also by an unknown mechanism.
Update Oct 2018 : â€śJohnson & Johnson has submitted its esketamine for regulatory approval, but researchers still don't understand how the fast-acting antidepressant lifts moods.â€ť Nature Reviews Drug Discovery volume 17, pages 773â€“775
Also see:and and
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