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. Author manuscript; available in PMC: 2016 Apr 1.
Published in final edited form as: Microcirculation. 2015 Apr;22(3):183–196. doi: 10.1111/micc.12190

Table 1.

KIR channel Ba2+ sensitivity, K+ activation and subunit distribution throughout the neurovascular unit. This table is not exhaustive, as some channels are formed from heteromeric subunit assemblies. Molecular studies for many subunits have not been performed for PAs, although pharmacological data are consistent with the expression of KIR channels that are activated by external K+ and blocked by <100 μM Ba2+ (i.e., KIR2 channels). Ba2+ blockade is voltage-sensitive, and where data are available we have listed IC50 values for negative potentials (note that the highly positive voltages listed for KIR1.1 and 6.1 mean that IC50 values at more negative potentials will be lower).

Isoform Rectification Ba2+ IC50 (nM) Voltage (mV) [K+]o (mM) K+-activated?* NVU expression* Refs
KIR1.1 Weak 4300 0 100 Yes Neurons Astrocytes Parenchymal arteriole [3,12,23,48,70,110]
n.d. n.d
KIR2.1 Strong 3.2 −100 60 Yes [17,26,39,47,65,67,107,108]
KIR2.2 Strong 0.5 −100 60 Yes [17,26,39,47,65,67,107,108]
KIR2.3 Strong 10.3 −100 60 Yes n.d. [17,39,47,65,107,108]
KIR2.4 Strong 390 −80 96 n.d ✓ - cranial nerve nuclei x n.d. [17,65,123]
KIR3.1 Strong 14 (+3.4) a −130 90 No n.d. [9,47,59,80]
KIR3.2 Strong n.d. b No x n.d. [9,47,80]
KIR3.3 Strong n.d. No x n.d. [9,47,80]
K|r3.4 Strong 92 −60 100 No x n.d. [9,45,47,80]
K|r4.1 Intermediate 7.1 −130 50 No x n.d. [9,22,38,108]
KIR4.2 Intermediate n.d. b Yes x x n.d. [38,94]
KIR5.1 Strong n.d. b n.d ✓ - cell culture n.d. [38,108,121]
KIR6.1 Weak 89.3 +60 5.4 No x x [16,41,122]
KIR6.2 Weak 29.3 (+SUR1) −102 5.6 No x x [16,32,81,117,118,122]
K|r7.1 Weak 1100-1900 −110 150 No n.d [19,55,92]
*

K+-activation is defined as an increase in channel conductance in the presence of elevated [K+]o at a constant electrical driving force.

#

All brain regions considered, where it is known that expression is highly restricted this is noted. No distinction is made between the smooth muscle and endothelial expression of KIR subunits in parenchymal arterioles due to the current lack of evidence.

✓ = expression confirmed, x = lack of expression observed. n.d. = not investigated to date, to the authors’ knowledge.

a

KIR3.1 homomers are non-functional, association with other KIR3.x subunits is required for functional channels [39].

b

KIR3.2 [114], 4.2 [94] and 5.1 [121] homomers are all inhibited by Ba2+ ions, but IC50 data are currently lacking.