Results 31 to 40 of about 5,435 (219)

The neonatal splice variant of Nav1.5 potentiates in vitro invasive behaviour of MDA-MB-231 human breast cancer cells [PDF]

open access: yes, 2007
Upregulation of functional voltage-gated Na+ channels (VGSCs) occurs in metastatic human breast cancer (BCa) in vitro and in vivo. The present study aimed to ascertain the specific involvement of the 'neonatal' splice variant of Nav1.5 (nNav1.5), thought
Brackenbury, William J.   +3 more
core   +1 more source

Activity of Palythoa caribaeorum Venom on Voltage-Gated Ion Channels in Mammalian Superior Cervical Ganglion Neurons

open access: yesToxins, 2016
The Zoanthids are an order of cnidarians whose venoms and toxins have been poorly studied. Palythoa caribaeorum is a zoanthid commonly found around the Mexican coastline. In this study, we tested the activity of P.
Fernando Lazcano-Pérez   +5 more
doaj   +1 more source

An update on transcriptional and post-translational regulation of brain voltage-gated sodium channels [PDF]

open access: yes, 2015
Voltage-gated sodium channels are essential proteins in brain physiology, as they generate the sodium currents that initiate neuronal action potentials.
Beltran-Alvarez, Pedro   +1 more
core   +1 more source

High-throughput electrophysiological assays for voltage gated ion channels using SyncroPatch 768PE. [PDF]

open access: yesPLoS ONE, 2017
Ion channels regulate a variety of physiological processes and represent an important class of drug target. Among the many methods of studying ion channel function, patch clamp electrophysiology is considered the gold standard by providing the ultimate ...
Tianbo Li   +5 more
doaj   +1 more source

Pain without Nociceptors? Nav1.7-Independent Pain Mechanisms

open access: yesCell Reports, 2014
Nav1.7, a peripheral neuron voltage-gated sodium channel, is essential for pain and olfaction in mice and humans. We examined the role of Nav1.7 as well as Nav1.3, Nav1.8, and Nav1.9 in different mouse models of chronic pain.
Michael S. Minett   +6 more
doaj   +1 more source

Pain-causing stinging nettle toxins target TMEM233 to modulate NaV1.7 function

open access: yesNature Communications, 2023
Voltage-gated sodium (NaV) channels are critical regulators of neuronal excitability and are targeted by many toxins that directly interact with the pore-forming α subunit, typically via extracellular loops of the voltage-sensing domains, or residues ...
Sina Jami   +39 more
doaj   +1 more source

Tarantula Toxin SGTx-1 alters Gating Kinetics of Human Voltage-Gated Sodium Channel Nav1.7 [PDF]

open access: yesBiophysical Journal, 2017
Voltage-gated sodium (Nav) channels play a key role in action potential generation in excitable cells and are targets of invertebrate toxins and therapeutics. The tarantula toxin SGTx-1 has been shown to target the domain IV voltage sensor (VSDIV) of Nav1.2, prolonging the macroscopic sodium current elicited during whole-cell voltage clamp experiments.
Ian H. Kimball   +6 more
openaire   +1 more source

Cell specific regulation of NaV1.7 activity and trafficking in rat nodose ganglia neurons

open access: yesNeurobiology of Pain, 2022
The voltage-gated sodium NaV1.7 channel sets the threshold for electrogenesis. Mutations in the gene encoding human NaV1.7 (SCN9A) cause painful neuropathies or pain insensitivity. In dorsal root ganglion (DRG) neurons, activity and trafficking of NaV1.7
Santiago I. Loya-López   +6 more
doaj   +1 more source

Extracellular signal-regulated kinases mediate the enhancing effects of inflammatory mediators on resurgent currents in dorsal root ganglion neurons [PDF]

open access: yes, 2019
Previously we reported that a group of inflammatory mediators significantly enhanced resurgent currents in dorsal root ganglion neurons. To understand the underlying intracellular signaling mechanism, we investigated the effects of inhibition of ...
Cummins, Theodore R.   +6 more
core   +1 more source

Nonsteroidal Anti-Inflammatory Drugs as Modulators of Cation Channels: Fenamates Repurposing in Channelopathies. [PDF]

open access: yesChemMedChem
Beyond their established role as nonsteroidal anti‐inflammatory drugs (NSAIDs), fenamates (niflumic, flufenamic, mefenamic, meclofenamic, and tolfenamic acids) have recently been identified as modulators of cationic ion channels. This review highlights their differential effects on ion channel activity and explores their potential for repurposing in ...
Laghetti P   +4 more
europepmc   +2 more sources

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