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Synergistic Inhibition of Delayed Rectifier K+ and Voltage-Gated Na+ Currents by Artemisinin in Pituitary Tumor (GH3) Cells
by
So, Edmund Cheung
, Yang, Chia-Jung
, Wu, Ping-Ching
, Chen, Hui-Zhen
, Wu, Sheng-Nan
in
Action potential
/ Action Potentials - drug effects
/ Animals
/ Artemisinin
/ Artemisinins - pharmacology
/ Brain cancer
/ Current kinetics
/ Delayed Rectifier Potassium Channels - antagonists & inhibitors
/ Delayed Rectifier Potassium Channels - metabolism
/ Delayed-rectifier K+ current
/ Dopamine
/ Dose-Response Relationship, Drug
/ Experiments
/ Growth models
/ Lactones - pharmacology
/ Medical research
/ Neoplasm Proteins - antagonists & inhibitors
/ Neoplasm Proteins - metabolism
/ Original Paper
/ Pituitary cell
/ Pituitary gland
/ Pituitary Neoplasms - drug therapy
/ Pituitary Neoplasms - metabolism
/ Pituitary Neoplasms - pathology
/ Potassium
/ Prolactinoma - drug therapy
/ Prolactinoma - metabolism
/ Prolactinoma - pathology
/ Rats
/ Tumors
/ Voltage-gated Na+ current
2017
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Synergistic Inhibition of Delayed Rectifier K+ and Voltage-Gated Na+ Currents by Artemisinin in Pituitary Tumor (GH3) Cells
by
So, Edmund Cheung
, Yang, Chia-Jung
, Wu, Ping-Ching
, Chen, Hui-Zhen
, Wu, Sheng-Nan
in
Action potential
/ Action Potentials - drug effects
/ Animals
/ Artemisinin
/ Artemisinins - pharmacology
/ Brain cancer
/ Current kinetics
/ Delayed Rectifier Potassium Channels - antagonists & inhibitors
/ Delayed Rectifier Potassium Channels - metabolism
/ Delayed-rectifier K+ current
/ Dopamine
/ Dose-Response Relationship, Drug
/ Experiments
/ Growth models
/ Lactones - pharmacology
/ Medical research
/ Neoplasm Proteins - antagonists & inhibitors
/ Neoplasm Proteins - metabolism
/ Original Paper
/ Pituitary cell
/ Pituitary gland
/ Pituitary Neoplasms - drug therapy
/ Pituitary Neoplasms - metabolism
/ Pituitary Neoplasms - pathology
/ Potassium
/ Prolactinoma - drug therapy
/ Prolactinoma - metabolism
/ Prolactinoma - pathology
/ Rats
/ Tumors
/ Voltage-gated Na+ current
2017
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Synergistic Inhibition of Delayed Rectifier K+ and Voltage-Gated Na+ Currents by Artemisinin in Pituitary Tumor (GH3) Cells
by
So, Edmund Cheung
, Yang, Chia-Jung
, Wu, Ping-Ching
, Chen, Hui-Zhen
, Wu, Sheng-Nan
in
Action potential
/ Action Potentials - drug effects
/ Animals
/ Artemisinin
/ Artemisinins - pharmacology
/ Brain cancer
/ Current kinetics
/ Delayed Rectifier Potassium Channels - antagonists & inhibitors
/ Delayed Rectifier Potassium Channels - metabolism
/ Delayed-rectifier K+ current
/ Dopamine
/ Dose-Response Relationship, Drug
/ Experiments
/ Growth models
/ Lactones - pharmacology
/ Medical research
/ Neoplasm Proteins - antagonists & inhibitors
/ Neoplasm Proteins - metabolism
/ Original Paper
/ Pituitary cell
/ Pituitary gland
/ Pituitary Neoplasms - drug therapy
/ Pituitary Neoplasms - metabolism
/ Pituitary Neoplasms - pathology
/ Potassium
/ Prolactinoma - drug therapy
/ Prolactinoma - metabolism
/ Prolactinoma - pathology
/ Rats
/ Tumors
/ Voltage-gated Na+ current
2017
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Synergistic Inhibition of Delayed Rectifier K+ and Voltage-Gated Na+ Currents by Artemisinin in Pituitary Tumor (GH3) Cells
Journal Article
Synergistic Inhibition of Delayed Rectifier K+ and Voltage-Gated Na+ Currents by Artemisinin in Pituitary Tumor (GH3) Cells
2017
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Overview
Background: Artemisinin (ART) is an anti-malarial agent reported to influence endocrine function. Methods: Effects of ART on ionic currents and action potentials (APs) in pituitary tumor (GH 3 ) cells were evaluated by patch clamp techniques. Results: ART inhibited the amplitude of delayed-rectifier K + current (I K(DR) ) in response to membrane depolarization and accelerated the process of current inactivation. It exerted an inhibitory effect on I K(DR) with an IC 50 value of 11.2 µM and enhanced I K(DR) inactivation with a K D value of 14.7 µM. The steady-state inactivation curve of I K(DR) was shifted to hyperpolarization by 10 mV. Pretreatment of chlorotoxin (1 µM) or iloprost (100 nM) did not alter the magnitude of ART-induced inhibition of I K(DR) in GH 3 cells. ART also decreased the peak amplitude of voltage-gated Na + current (I Na ) with a concentration-dependent slowing in inactivation rate. Application of KMUP-1, an inhibitor of late I Na , was effective at reversing ART-induced prolongation in inactivation time constant of I Na . Under current-clamp recordings, ART alone reduced the amplitude of APs and prolonged the duration of APs. Conclusion: Under ART exposure, the inhibitory actions on both I K(DR) and I Na could be a potential mechanisms through which this drug influences membrane excitability of endocrine or neuroendocrine cells appearing in vivo.
Publisher
S. Karger AG,Cell Physiol Biochem Press GmbH & Co KG
Subject
/ Action Potentials - drug effects
/ Animals
/ Delayed Rectifier Potassium Channels - antagonists & inhibitors
/ Delayed Rectifier Potassium Channels - metabolism
/ Delayed-rectifier K+ current
/ Dopamine
/ Dose-Response Relationship, Drug
/ Neoplasm Proteins - antagonists & inhibitors
/ Neoplasm Proteins - metabolism
/ Pituitary Neoplasms - drug therapy
/ Pituitary Neoplasms - metabolism
/ Pituitary Neoplasms - pathology
/ Rats
/ Tumors
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