sodium channels การใช้

• Phenytoin binds preferentially to the inactive form of the sodium channel.
• Aconitine is a potent neurotoxin that opens tetrodotoxin sensitive sodium channels.
• For example, in Brugada Syndrome, sodium channels are affected.
• Sodium channels have similar functional properties across many different cell types.
• A remotely related group of atracotoxins operate by opening sodium channels.
• In addition, BcTx1 slows down the activation of sodium channels.
• All of the peptides are voltage-gated sodium channel blockers.
• The ?3 subunit can increase persistent current in certain sodium channels.
• The voltage-gated sodium channel is essential for normal neuronal functioning.
• Aconitine is a potent neurotoxin that opens tetrodotoxin-sensitive sodium channels.
• The voltage gated sodium channel is composed of 1980 residues.
• Typical action potentials are initiated by voltage gated sodium channels.
• JZTX-I does not affect the activation threshold of sodium channels.
• Aldosterone activates sodium channels that result in sodium resorption from the urine.
• Other hainantoxins bind at site 3 of the sodium channels.
• Mutations in genes encoding the cardiac sodium channels affect inactivation.
• Sodium channel blocker lists both extracellular and intracellular classes of these substances.
• It functions by opening sodium channels in the insect's nerve cells.
• The effect on sodium channels could be of particular relevance for seizure protection.
• Bifenthrin will open the sodium channel for a shorter period than other pyrethroids.