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  4. Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Na1.4 channel.
 
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Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Na1.4 channel.

Journal
Pesticide Biochemistry and Physiology
Journal Volume
200
Start Page
105833
ISSN
0048-3575
Date Issued
2024-03
Author(s)
HSING-JUNG LAI  
MING-JEN LEE  
Yu, Hsin-Wei
Tsai, Ke-Li
KUAN-WEN CHEN  
Lin, Pi-Chen
Huang, Chiung-Wei
DOI
10.1016/j.pestbp.2024.105833
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/734799
Abstract
Human skeletal muscle contraction is triggered by activation of Na1.4 channels. Na1.4 channels can generate resurgent currents by channel reopening at hyperpolarized potentials through a gating transition dependent on the intracellular Naβ4 peptide in the physiological conditions. Tefluthrin (TEF) is a pyrethroid insecticide that can disrupt electrical signaling in nerves and skeletal muscle, resulting in seizures, muscle spasms, fasciculations, and mental confusion. TEF can also induce tail currents through other voltage-gated sodium channels in the absence of Naβ4 peptide, suggesting that muscle spasms may be caused by resurgent currents. Further, intracellular Naβ4 peptide and extracellular TEF may show competitive or synergistic effects; however, their binding sites are still unknown. To address these issues, electrophysiological recordings were performed on CHO-K1 cells expressing Na1.4 channels with intracellular Naβ4 peptide, extracellular TEF, or both. TEF and Naβ4 peptide induced a hyperpolarizing shift of activation and inactivation curves in the Na1.4 channel. TEF also substantially prolonged the inactivation time constants, while simultaneous application of Naβ4 peptide partially reversed this effect. Resurgent currents were enhanced by TEF and Naβ4 peptide at negative potentials, but TEF more potently enhances resurgent currents and dampens decay of resurgent currents. With longer depolarization, peak resurgent currents decay was fastest with the TEF alone. Molecular docking suggested that TEF and Naβ4 peptide binding site(s) are not in the narrowest part of the channel pore, but rather in the bundle-crossing regions and in the domain linkers, respectively. TEF can induce resurgent currents independently and synergistically with Naβ4 peptide, which may explain the muscle spasms observed in TEF intoxication.
Subjects
Gating changes
Na(v)1.4 channel
Na(v)β4 peptide
Resurgent current
Tefluthrin
SDGs

[SDGs]SDG3

Type
journal article

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