Table 1.
Publication | Test Subject | Study Design | Antidepressant-Like Effect | Molecular Mechanism |
---|---|---|---|---|
Franceschelli et al., 2015 [64] | Male and female C57/BL6J mice | KET in naïve and CMS animals: female and male mice (FST) | KET effect: Female mice > male mice | Effects on excitatory amino acids (glutamate and aspartate), serotoninergic activity. |
Saland et al., 2018 [65] | Male and female Sprague-Dawley rats | KET metabolism and distribution | ↑ level of KET and NK in both brain and plasma | |
Ho et al., 2018 [66] | Human iPSC-derived astrocytes | Oestrogen + KET in vitro | Oestrogens augmented the effect of KET | ↑ level of AMPA receptor subunit and ERα. Oestrogens: ↑ level of CYP2A6 and CYP2B6. |
Dossat et al., 2018 [67] | Male and female C57/BL6J mice | Oestrogen and Progesterone receptor agonist and KET (FST) | Female in proestrus + KET: sensitive to lower dose. | Proestrus female ↑ p-Akt and p-CaMKIIα. |
Sarkar et al. 2016 [28] | Male and female Sprague-Dawley rats | KET and social isolation stress (behaviour and synaptic protein level) | IS: male depression like behaviour at 8 weeks while female at 11 weeks. KET rescued the phenotype. | Decline in spine density and synaptic proteins reversed by KET only in male but not female |
We list relevant, ketamine-associated publications with significant impact in the field. KET ketamine, CMS chronic mild stress, FST forced swim test, NK norketamine, iPSC induced Pluripotent Stem Cells, AMPA α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor, CYP Cytochrom P 450 Enzyme, IS Isolation Stress.