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. 2005 May 12;565(Pt 3):751–756. doi: 10.1113/jphysiol.2005.087312

Table 1.

Ito current characteristics in CHO expression systems with coexpression of KChIP2a and DPPX, 22°C

Kv4.3 + KChIP2aa n Kv4.3 + DPPXb n Kv4.3 + KChIP2a + DPPXc n Humanventricularmyocytesd n
Cm (pF) 33 ± 3 40 12 ± 2 8 39 ± 6 18 292 ± 22 28
Im current density at +50 mV (pA pF−1) 495 ± 86 26 399 ± 90 6 373 ± 50 15 7.9 ± 0.7 28
τfast of inactivation at +50 mV (ms) 55 ± 4 11 25 ± 6* 8 45 ± 6 10 54 ± 3 5
(58 ± 3) (28)
τslow of inactivation at +50 mV (ms) 392 ± 160 10 177 ± 16 8 427 ± 213 10 n.d.
V0.5 of steady-stateinactivation (mV) −31.3 ± 2.4 24 −57.0 ± 3.1* 8 −39.8 ± 2.8 9 −45.5 ± 1.2 5
(−30.4 ± 1.2) (26)
Slope k of steady-state inactivation (mV) −5.0 ± 0.5 24 −5.5 ± 0.4 8 −6.6 ± 0.6 9 −4.6 ± 0.8 5
(−4.5 ± 0.2) (26)
τfast of recovery from inactivation at+50 mV, from −80 mV (ms) 42 ± 8 11 52 ± 16 8 18 ± 3* 11 24 ± 3 6
at +20 mV,from −100 mV
*

Values significantly different from other groups P < 0.05.

a

Stable expression of Kv4.3 and KChiP2a.

b

Stable expression of Kv4.3 and transient expression of DPPX.

c

Stable expression of Kv4.3 and KChiP2a and transient expression of DPPX.

d

Data from Wettwer et al. (1994) for comparison, not included in statistical analysis; subepicardial myocytes, nifedipine (1 μm) or Cd2+ (0.1 mm, data in brackets) was used for block of ICa. n.d. values not determined.