NDLI: Modulation of a cloned human A-type voltage-gated potassium channel (hKv1.4) by the protein tyrosine kinase inhibitor genistein

Content Provider	Springer Nature Link
Author	Zhang, Zhi Hao Wang, Qiang
Copyright Year	2000
Abstract	A cloned, human, A-type, voltage-gated potassium channel (hKv1.4) was expressed transiently in Chinese hamster ovary cells and the effects of the broad-spectrum tyrosine kinase inhibitor genistein on hKv1.4 were studied using the whole-cell patch-clamp recording method. Genistein (up to 50 µM) reversibly reduced the peak currents of hKv1.4 by 44.9±12%. In addition, genistein markedly slowed the activation kinetics (time constant τa) of hKv1.4. At +50 mV, τa increased from 1.8±0.3 to 5.0±0.6 ms (P<0.01). The effect of genistein on the channel inactivation kinetics (time constant τi) was more complex, in that τi was increased significantly at lower step potentials but unaltered at +50 mV or more depolarized potentials. Tail current analysis showed that genistein had no effect on the kinetics of deactivation (time constant τd), but shifted the steady-state activation curve significantly to the right by about 15 mV (potential for half-maximal activation, V 1/2, changed from –7.4±4.4 to +7.7±2.7 mV) with a moderate change in the slope (k) of the curve (from 17.4±2.2 to 23±1.0 mV, P<0.05). Genistein slightly altered the slope of the steady-state inactivation curve from –5.5±0.4 to –7.5±0.4 mV (P<0.01). The recovery rate from inactivation was not altered by genistein. The tyrosine phosphatase inhibitor orthovanadate (1 mM) alone had little impact on current amplitude or channel kinetics. However, orthovanadate significantly, but not completely, blocked the effect of genistein on current amplitude (by 25.5%) and kinetics (by 67.1%). Daidzein (up to 50 µM), an inactive analogue of genistein, had no effect on current amplitude or kinetics. In contrast to genistein, another tyrosine kinase inhibitor, herbimycin A, had little effect on the channel peak amplitude or kinetics. In addition, genistein had a similar impact on the channel peak current amplitude and kinetics in cells with or without pre-treatment with herbimycin A (10 µM). The data suggest that genistein-induced inhibition of tyrosine phosphorylation may not be the exclusive mechanism by which hKv1.4 is down-regulated and channel gating affected. Genistein may produce a non-catalytic blockade of this channel.
Starting Page	784
Ending Page	792
Page Count	9
File Format	PDF
ISSN	00316768
Journal	Pflügers Archiv
Volume Number	440
Issue Number	5
e-ISSN	14322013
Language	English
Publisher	Springer-Verlag
Publisher Date	2000-07-04
Publisher Place	Berlin, Heidelberg
Access Restriction	One Nation One Subscription (ONOS)
Subject Keyword	Human Physiology
Content Type	Text
Resource Type	Article
Subject	Physiology Physiology (medical) Clinical Biochemistry

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