The role of glutamatergic modulation in the mechanism of action of ketamine, a prototype rapid-acting antidepressant drug

• Published in: Pharmacological reports 2018-10, Vol.70 (5), p.837-846
• Main Author: Pałucha-Poniewiera, Agnieszka
• Format: Article
• Language: English
• Subjects: (R)-ketamine; (S)-ketamine; AMPA receptor; Animals; Antidepressant; Antidepressive Agents - pharmacology; Depression; Disease Models, Animal; Drug Safety and Pharmacovigilance; Excitatory Amino Acid Agents - pharmacology; Glutamic Acid - metabolism; Humans; Ketamine; Ketamine - analogs & derivatives; Ketamine - pharmacology; Ketamine - therapeutic use; mGlu receptor; NMDA receptor; Pharmacotherapy; Pharmacy; Receptors, AMPA - agonists; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors; Review Article; Synapses - drug effects
• ISSN: 1734-1140; 2299-5684
• DOI: 10.1016/j.pharep.2018.02.011

Over the past decade, ketamine has been one of the most commonly studied potential antidepressants. This is because it produces a spectacularly rapid and persistent therapeutic effect in people suffering from severe treatment-resistant depression (TRD), for which classical drugs are ineffective. Similar efficacy was demonstrated for scopolamine, a drug belonging to a completely different pharmacological group. This interesting coincidence piqued the interest of psychopharmacologists and prompted them to search for a possible common mechanism of these rapid acting antidepressant drugs (RAADs). A thorough explanation of this mechanism is also important because each of these substances induces serious side effects. Knowing the mechanism responsible for the therapeutic efficacy of RAADs could lead to minimizing, or even avoiding certain undesirable effects. This review provides an overview of the mechanism of action of a prototype RAAD, ketamine, in animal models, with a particular focus on the roles of NMDA receptors, AMPA receptors, synaptogenesis, and modulation of glutamate transmission by other modulators of this system, such as mGlu receptor ligands. Recently studied roles for ketamine enantiomers and metabolites in its rapid antidepressant effect are also considered. Finally, the results of multiple clinical trials are reported and discussed in relation to basic research. This review concludes that success in introducing novel therapeutic RAADs will depend on better cooperation and integration of neuroscience research and clinical practice.