Visceral Pain

Vagal afferents convey predominantly physiological information, while spinal afferents convey noxious stimuli.

There are likely to be three types of nociceptive sensory receptors: High threshold noxious, Low threshold innocuous to noxious, while some are silent and recruited by tissue injury and inflammation.

All can be sensitized, and drive central sensitisation that can persist even after the initial insult has resolved. Damage and inflammation also affects normal motility and secretion, producing changes to the nociceptor environment. While ascending pathways include the spinothalamic tract, the dorsal column is more important in nociceptive transmission. Ascending tracts synapse at the thalamus, limbic centres, and the somatosensory cortex. There is no somatotropic representation in the cortex. Pain is represented in the secondary somatosensory cortex. Visceral pain elicits nausea and hypotension, the opposite to somatic pain.

Peripheral sensitisation can occur, but the mechanisms differ from cutaneous sensitisation. Functional visceral disturbance can persist even after the initial insult has resolved. While with central sensitisation, NMDA receptors are likely to play significant role.

Visceral pain is initially described as vague, central sensation felt anterior or posterior, accompanied by various neurovegetative symptoms such as malaise, nausea, sweating, palour , anxiety, and sense of impending doom (‘true visceral pain’). Eventually this subsides, and is followed by a variety of symptoms and signs perceived in somatic areas receiving the same innervation. Skin, subcutis and muscle are all involved. Initially, the symptoms of pain rather than pain itself is felt. As time progresses, signs start to develop. The muscle layer is earliest and most commonly involved layer. However, the skin and subcutaneous layers are also commonly involved with hyperalgesia, and sudomotor signs. These symptoms and signs can persist even when the visceral insult has resolved. These symptoms and signs may also, in turn, influence visceral symptoms.