Circumspectives: the promise of ketamine
Circumspectives: the promise of ketamine"
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In this issue we reprise a Feature called _Circumspectives_. The general format of a _Circumspectives_ article is similar to a debate, with separate sections in which two thought leaders
articulate their individual positions on a topic of great importance to our community of researchers. The distinguishing element, however, is that the piece ends with a ‘reconciliation’ that
is co-authored by both and includes ideas or experiments that will move the field forward. The current _Circumspectives_ (Sanacora and Schatzberg, 2015) is entitled ‘Ketamine: Promising
Path or False Prophecy in the Development of Novel Therapeutics for Mood Disorders?’. It is co-authored by Gerard Sanacora and Alan F Schatzberg, who are leaders in this field. The article
is insightfully written and intended to promote a collegial and productive exchange of ideas regarding the impact that ketamine has had in psychiatry within the last decade, as well as
recommendations for the future. Dr Sanacora describes the history of clinical studies of ketamine as an antidepressant, and how the discovery that it produces rapid and robust antidepressant
effects in patients with severe (treatment-resistant) depression has changed our thinking. Perhaps the most important legacy of this discovery is that there is now a greater appreciation
for the fact that it is possible to design a therapeutic regimen that produces rapid antidepressant effects. At the time of the seminal ketamine report (Zarate et al, 2006), the prevailing
dogma was that all antidepressant therapies required a time lag of several weeks to become effective. The finding that standard antidepressants stimulate adult hippocampal neurogenesis, a
process that requires weeks for new cells to be born and differentiate into neurons, provided a compelling explanation for both the therapeutic effects of the drugs as well as their time lag
(Dranovsky and Hen, 2006). The neurogenesis hypothesis has justifiably had a tremendous influence on research and drug development strategies. However, the discovery that ketamine has rapid
antidepressant effects in humans—detectable within hours of administration—demonstrated that neurogenesis is not required for an antidepressant response, thereby providing a prominent
exception to an influential hypothesis and offering hope that fast-acting but safe antidepressants are possible. Despite growing enthusiasm for ketamine and its promise, Dr Schatzberg
describes some sobering details and gaps in knowledge. Ketamine is a drug of abuse and, despite some exceptionally elegant studies on the mechanism (eg, Li et al, 2010; Autry et al, 2011),
there is no consensus on how it produces therapeutic effects. As one example, Dr Schatzberg points out similarities in some of the molecular actions of ketamine and scopolamine, another
familiar and long-standing member of our phamacopea shown to produce rapid antidepressant effects (Furey and Drevets, 2006). It is interesting that the broad classes of agents to which
ketamine and scopolamine belong (NMDA antagonists and muscarinic acetylcholine antagonists, respectively) have long been used by behavioral phamacologists to disrupt learning and memory
processes in laboratory animals, making it conceivable that, despite common actions on discrete molecules, their key similarity is on more general circuit function, and that a tendency to
disrupt memory is what provides relief to patients with treatment-resistant depression. Perhaps the most provocative aspect of Dr Schatzberg’s piece, however, lies in his rhetorical
question: is it important to understand ketamine’s mechanism of action? This question will be welcomed by some and viewed as heresy by others—which, incidentally, is exactly the intention of
_Circumspectives_. The question should provoke thought when considering the history of research on antidepressants and the current state of neuroscience research and development in the
pharmaceutical industry. Decades of research and billions of dollars have been invested toward understanding the mechanisms by which drugs such as fluoxetine produce their therapeutic
effects. Despite these efforts, there is still no consensus on which of their myriad actions are most crucial, there are currently no major breakthroughs that can trace their heritage to
this massive investment, and leading pharmaceutical companies have elected to divest of this type of research. These facts give weight to our rhetorical answer that it may be easier and more
fruitful to focus on how the brain works than on how the drugs work. The individuals who played key roles in the conceptualization, development, and implementation of this article include
Amit Etkin, Tony George, and Gerard Sanacora. The Editors welcome suggestions for future _Circumspectives_ topics and authors, which can be submitted to [email protected]. Please note that
unsolicited articles of this type will not be considered. We envision publishing 1–2 of these Features each year; the next one is already underway. FUNDING AND DISCLOSURE The authors declare
no conflict of interest. REFERENCES * Autry AE, Adachi M, Nosyreva E, Na ES, Los MF, Cheng PF _et al_ (2011). NMDA receptor blockade at rest triggers rapid behavioural antidepressant
responses. _Nature_ 475: 91–95. Article CAS Google Scholar * Dranovsky A, Hen R (2006). Hippocampal neurogenesis: regulation by stress and antidepressants. _Biol Psychiatry_ 59:
1136–1143. Article CAS Google Scholar * Furey ML, Drevets WC (2006). Antidepressant efficacy of the antimuscarinic drug scopolamine: a randomized, placebo-controlled clinical trial. _Arch
Gen Psychiatry_ 63: 1121–1129. Article CAS Google Scholar * Li N, Lee B, Liu RJ, Banasr M, Dwyer JM, Iwata M _et al_ (2010). mTOR-dependent synapse formation underlies the rapid
antidepressant effects of NMDA antagonists. _Science_ 329: 959–964. Article CAS Google Scholar * Sanacora G, Schatzberg AF (2015). Ketamine: promising path or false prophecy in the
development of novel therapeutics for mood disorders? _Neuropsychopharmacology_ (this issue). * Zarate CA Jr, Singh JB, Carlson PJ, Brutsche NE, Ameli R, Luckenbaugh DA _et al_ (2006). A
randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression. _Arch Gen Psychiatry_ 63: 856–864. Article CAS Google Scholar Download references AUTHOR
INFORMATION AUTHORS AND AFFILIATIONS * Department of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA, USA William A Carlezon * Department of Psychiatry, University of
Toronto, Toronto, Ontario, Canada Tony P George Authors * William A Carlezon View author publications You can also search for this author inPubMed Google Scholar * Tony P George View author
publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to William A Carlezon. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS
ARTICLE CITE THIS ARTICLE Carlezon, W., George, T. Circumspectives: The Promise of Ketamine. _Neuropsychopharmacol_ 40, 257–258 (2015). https://doi.org/10.1038/npp.2014.270 Download
citation * Published: 11 December 2014 * Issue Date: January 2015 * DOI: https://doi.org/10.1038/npp.2014.270 SHARE THIS ARTICLE Anyone you share the following link with will be able to read
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