Pain is mediated by functionally distinctive components. It may involv
e acute high threshold afferent stimuli (thermal, mechanical or chemic
ally damaged tissue), protracted afferent input (long-lasting hyperalg
esia) or low-threshold input (allodynia as related to pain from light
touch). Behavioral patterns will be associated with the effects of nox
ious stimulus on excitatory transmitters. Humane studies using mechani
cal, thermal (cold presser test), audio-evoked potentials, or other no
xious stimuli during anesthesia and analgesia provide clues to percept
ion of pain in animals and help us determine guidelines for the clinic
al relief of animal pain. There is a better understanding of cutaneous
somatosensory responses than for deep sensation (e.g., subcutaneous t
issue, muscle, bone, visceral. The prevention or treatment of pain can
best be accomplished when there is a diagnosis of the neuroanatomical
distribution of the pain based on evidence of sensory dysfunction inv
olving a peripheral nerve, plexus, nerve root or central pathway using
different modalities for quantitative sensory testing. Anatomical stu
dies have demonstrated that unmyelinated primary afferent fibers conta
in a variety of neuroactive substances which may be released by high-i
ntensity peripheral stimulation. Fast depolarization of the dorsal hor
n nociresponsive neurons is mediated by tissue damage. These neurorece
ptors may be activated by glutamate, substance P, and neurokinin A. Th
e major ascending pathway relaying nociceptive information relating to
pain is the spinothalamic tract. Most of the neurons in this tract ar
e nociceptive or thermoreceptive. The thalamus is the final relay nucl
eus for all the sensory systems, except olfactory tissue. Injury or di
sease processes in deeper tissue or visceral areas with extensive inne
rvation may result in pain thresholds not adequately controlled by cur
rent available analgesics or at their recommended dosage levels. These
issues are complex and diagnosis is even more difficult due to specie
s and breed differences in outward expression to painful insult. Medic
ations can now be targeted for specific receptors. (C) 1998 Elsevier S
cience B.V. All rights reserved.