Protein Information

ID 3961
Name Kir4.1
Synonyms ATP sensitive inward rectifier potassium channel 10; ATP dependent inwardly rectifying potassium channel Kir4.1; BIRK 10; Glial inwardly rectifying potassium channel Kir4.1; Inward rectifier K(+) channel Kir1.2; Inward rectifier K+ channel Kir1.2; KCNJ10; KCNJ13 PEN…

Compound Information

ID 955
Name TCA
CAS 2,2,2-trichloroacetic acid

Reference

PubMed Abstract RScore(About this table)
17071817 Su S, Ohno Y, Lossin C, Hibino H, Inanobe A, Kurachi Y: Inhibition of astroglial inwardly rectifying Kir4.1 channels by a tricyclic antidepressant, nortriptyline. J Pharmacol Exp Ther. 2007 Feb;320(2):573-80. Epub 2006 Oct 27.
The inwardly rectifying K (+) (Kir) channel Kir4.1 is responsible for astroglial K (+) buffering. We examined the effects of nortriptyline, a tricyclic antidepressant (TCA), on Kir4.1 channel currents heterologously expressed in HEK293T cells, using a whole-cell patch-clamp technique. Nortriptyline (3-300 microM) reversibly inhibited Kir4.1 currents in a concentration-dependent manner, whereas it marginally affected neuronal Kir2.1 currents. The inhibition of Kir4.1 channels by nortriptyline depended on the voltage difference from the K (+) equilibrium potential (E (K)), with greater potency at more positive potentials. Blocking kinetics of the drug could be described by first-order kinetics, where dissociation of the drug slowed down and association accelerated as the membrane was depolarized. The dissociation constant (K (d)) of nortriptyline for Kir4.1 inhibition was 28.1 microM at E (K). Other TCAs, such as amitriptyline, desipramine, and imipramine, also inhibited Kir4.1 currents in a similar voltage-dependent fashion. This study shows for the first time that nortriptyline and related TCAs cause a concentration-, voltage-, and time-dependent inhibition of astroglial K (+)-buffering Kir4.1 channels, which might be involved in therapeutic and/or adverse actions of the drugs.
8(0,0,0,8)