Abstract
Various types of ion channels are involved in the control of neuronal activity. Among them, SK channels represent an interesting therapeutic target. Indeed, they underlie medium duration after hyperpolarizations in many types of neurons, thus inhibiting cell excitability. A thorough knowledge of the physiology of these channels and the discovery of non-peptidic selective modulators able to cross the blood-brain barrier are essential in view of developing future drugs for brain diseases such as those related to a dysfunction of dopaminergic and serotonergic systems.
© 2012 médecine/sciences – Inserm / SRMS.
MeSH terms
-
Animals
-
Humans
-
Membrane Potentials / drug effects
-
Membrane Potentials / genetics
-
Membrane Potentials / physiology
-
Models, Biological
-
Models, Molecular*
-
Potassium / metabolism
-
Potassium Channel Blockers / pharmacology*
-
Potassium Channels / agonists*
-
Potassium Channels / chemistry*
-
Potassium Channels / genetics
-
Potassium Channels / physiology*
-
Small-Conductance Calcium-Activated Potassium Channels* / agonists
-
Small-Conductance Calcium-Activated Potassium Channels* / antagonists & inhibitors
-
Small-Conductance Calcium-Activated Potassium Channels* / chemistry
-
Small-Conductance Calcium-Activated Potassium Channels* / physiology
-
Substrate Specificity
Substances
-
Potassium Channel Blockers
-
Potassium Channels
-
Small-Conductance Calcium-Activated Potassium Channels
-
Potassium