Ocular irritation and pain are associated with many clinical situation
s (e.g. accidental injury, eye diseases, surgery and contact lens wear
ing). Pain and related ocular sensations begin with stimulation by inj
urious stimuli of first-order sensory neurons uf the trigeminal gangli
on. Neurons responding solely to application in their receptive field
of noxious mechanical forces (mechanonociceptive neurons), or of irrit
ant chemicals and heat (polymodal nociceptive neurons), have been iden
tified electrophysiologically in the conjunctiva, cornea, sclera, iris
, ciliary body and choroid. The cornea is additionally innervated by n
eurons responding to low temperatures, which may account for corneal d
iscomfort caused by cold. Also, low-threshold mechanoreceptive and col
d-sensitive neurons supply the conjunctiva and sclera, possibly mediat
ing touch and thermal sensations aroused by innocuous stimuli in the f
ront of the eye. Ocular sensory information is transmitted from the tr
igeminal ganglion to specific higher-order neurons located in the trig
eminal brainstem nuclear complex, the thalamus and the cerebral fortes
. Local ocular inflammatory responses enhance injury-induced neural ac
tivity both in ocular nociceptive terminals and in higher order neuron
s. In addition to signalling acute lesions, ocular primary sensory neu
rons participate in post-injury processes, contributing to local infla
mmatory reactions (neurogenic inflammation) and io the repair of damag
ed tissues. These effects are mediated at least in part, by substance
P and CGRP, two neuropeptides contained in ocular sensory nerves cells
that are released peripherally upon tissue damage. Ocular tissues hav
e a trophic interdependence with their sensory neurons. Ocular tissues
are the source of neurotrophic factors that are critical for the earl
y development and survival of trigeminal sensory neurons. On the other
hand, the morphofunctional integrity of some ocular tissues like the
contra. appears to be dependent on the presence of an intact sensory i
nnervation, Stimulation of ocular sensory pathways by noxious mechanic
al, chemical and thermal stimulation of cornea, conjunctiva or of othe
r eye structures, evokes distinct types of ocular sensations. Differen
ces in the quality of pain sensation presumably result from the magnit
udes of activation of the various sub-populations of ocular nociceptiv
e neurons by different stimulus modalities. In addition to conscious s
ensations, injurious stimuli evoke protective reflexes (blinking and l
acrimation) aimed at protecting the rye and minimizing further ocular
damage by noxious stimuli. Copyright (C) 1996 Elsevier Science Ltd.