Table 2.
Reference | Drug | Model | Kir4.1 Expression/Function |
---|---|---|---|
Su et al., 2007 [44] | TCAs | HEK293T cells | ↓ Kir4.1 |
Ohno et al., 2007 [45] | SSRIs | HEK293T cells | ↓ Kir4.1 |
Furutani et al., 2009 [52] | TCAs and SSRIs | Chimeric and site directed mutants of Kir4.1 expressed in Xenopus Laevis oocytes and computational analyses of three-dimensional arrangements of the ligands. | ↓ Kir4.1 interacting with channel pore residues |
Kinboshi et al., 2017 [53] | SSRIs, TCAs, mianserin, and siRNA | Primary mouse astrocytes | ↓ Kir4.1 and ↑ BDNF |
Stenovec et al., 2020 [46] | Ketamine | Rat cortex astrocytes | ↓ Kir4.1 reducing mobility of Kir4.1-carrying vesicles. |
Song et al., 2019 [51] and Song et al., 2021 [50] | Fluoxetine | Normal adult rats | ↓ Kir4.1 and ↑ BDNF |
TCAs: tricyclic antidepressants; SSRIs: selective serotonin reuptake inhibitors, siRNA: RNA silencing; BDNF: brain derived neurotrophic factor.