Damage-sensing neurons express a unique cohort of genes encoding channels a
nd receptors that play a role in nociception. However, there are redundant
pathways involved in, for example, inflammatory pain and many channels and
receptors have additional physiologic roles unrelated to nociception. Thus,
it is impossible to ascribe a particular sensory modality to the expressio
ns of a single molecular entity. Despite this, the relatively selective exp
ression of a number of channels and receptors in nociceptive neurons provid
e potentially interesting analgesic drug targets that can be examined throu
gh the generation of knockout mice.