Mammalian 2P domain K+ channels are responsible for background or 'leak' K currents. These channels are regulated by various physical and chemical st
imuli, including membrane stretch, temperature, acidosis, lipids and inhala
tional anaesthetics. Furthermore, channel activity is tightly controlled by
membrane receptor stimulation and second messenger phosphorylation pathway
s. Several members of this novel family of K+ channels are highly expressed
in the central and peripheral nervous systems in which they are proposed t
o play an important physiological role. The pharmacological modulation of t
his novel class of ion channels could be of interest for both general anaes
thesia and ischaemic neuroprotection.