Abstract
We have investigated the characteristics of voltage-gated K(+) channels and L-type Ca(2+) channels in GH3 rat pituitary cells and the effects of the xenoestrogen (XEs) nonylphenol (NP) on these ion channel currents. Our results have shown that the lower concentrations (10(-15)-10(-14)M) of NP decreased the amplitudes of voltage-gated K(+) currents (IKv) and activated L-type Ca(2+) currents (ICa-L) by reducing half-activation membrane potentials of activation kinetics curves. However, the higher concentrations (10(-10)-10(-9)M) of NP increased the amplitudes of IKv and inhibited ICa-L by reducing the peak values of ICa-L. Thus, NP affects IKv and ICa-L in an opposite and non-monotonic manner.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Action Potentials / drug effects
-
Animals
-
Calcium / metabolism
-
Calcium Channels, L-Type / drug effects
-
Calcium Channels, L-Type / metabolism*
-
Cell Line
-
Dose-Response Relationship, Drug
-
Electrophysiological Phenomena
-
Environmental Exposure / analysis
-
Estrogens / toxicity
-
Ion Channel Gating / drug effects*
-
Ion Channels / drug effects
-
Ion Channels / metabolism
-
Membrane Potentials
-
Patch-Clamp Techniques
-
Phenols / toxicity*
-
Pituitary Gland / cytology
-
Pituitary Gland / drug effects*
-
Pituitary Gland / metabolism
-
Potassium / metabolism
-
Potassium Channels, Voltage-Gated / drug effects
-
Potassium Channels, Voltage-Gated / metabolism*
-
Rats
Substances
-
Calcium Channels, L-Type
-
Estrogens
-
Ion Channels
-
Phenols
-
Potassium Channels, Voltage-Gated
-
nonylphenol
-
Potassium
-
Calcium