Ketamine and Ketamine Metabolite Pharmacology: Insights into Therapeutic Mechanisms
By P. Zanos, R. Moaddel, Patrick J. Morris, L. Riggs, Jaclyn N. Highland, Polymnia Georgiou, E. Pereira, E. Albuquerque, Craig J. Thomas, C. Zarate and 1 more. Pharmacological Reviews, 2018
1,059 citations recorded by the source corpus.
Ketamine, a racemic mixture consisting of (S)- and (R)-ketamine, has been in clinical use since 1970. Although best characterized for its dissociative anesthetic properties, ketamine also exerts analgesic, anti-inflammatory, and antidepressant actions. We provide a comprehensive review of these therapeutic uses, emphasizing drug dose, route of administration, and the time course of these effects. Dissociative, psychotomimetic, cognitive, and peripheral side effects associated with short-term or prolonged exposure, as well as recreational ketamine use, are also discussed. We further describe ketamine’s pharmacokinetics, including its rapid and extensive metabolism to norketamine, dehydronorketamine, hydroxyketamine, and hydroxynorketamine (HNK) metabolites. Whereas the anesthetic and analgesic properties of ketamine are generally attributed to direct ketamine-induced inhibition of N-methyl-D-aspartate receptors, other putative lower-affinity pharmacological targets of ketamine include, but are not limited to, γ-amynobutyric acid (GABA), dopamine, serotonin, sigma, opioid, and cholinergic receptors, as well as voltage-gated sodium and hyperpolarization-activated cyclic nucleotide-gated channels. We examine the evidence supporting the relevance of these targets of ketamine and its metabolites to the clinical effects of the drug. Ketamine metabolites may have broader clinical relevance than was previously considered, given that HNK metabolites have antidepressant efficacy in preclinical studies. Overall, pharmacological target deconvolution of ketamine and its metabolites will provide insight critical to the development of new pharmacotherapies that possess the desirable clinical effects of ketamine, but limit undesirable side effects.
Subfields: Biological Psychiatry, Cellular and Molecular Neuroscience, Pharmacology
View Paper: https://www.semanticscholar.org/paper/047c92eaa41fc88210eb47d1bc0dbb988c30314f
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In Biological Psychiatry
In Cellular and Molecular Neuroscience
In Pharmacology
Citations in the corpus
- Synthesizing the Evidence for Ketamine and Esketamine in Treatment-Resistant Depression: An International Expert Opinion on the Available Evidence and Implementation (2021, background): “In addition to effects on glutamate-GABAsystems, evidence suggests that other low-affinity targets may also be relevant to ketamine’s mechanism of action in TRD (34).”