Itch can originate in the
peripheral nervous system (
dermal or
neuropathic) or in the
central nervous system (neuropathic,
neurogenic, or
psychogenic).
Pruritoceptive Itch originating in the skin is known as
pruritoceptive, and can be induced by a variety of stimuli, including mechanical, chemical, thermal, and electrical stimulation, or infection. The primary
afferent neurons responsible for
histamine-induced itch are
unmyelinated C-fibres.
Gene expression. Using single-cell mRNA sequencing, clusters of genes expressed in itch-related tissues were identified, e.g. NP1-3, transmitting itch information; where NP3 expresses neuropeptides
Nppb and
Sst as well as genes involved in inflammatory itch (
Il31ra,
Osmr and Crystrl2). The histamine receptor gene
Hrh1 was found in NP2 and NP3, suggesting that histaminergic itch is transmitted by both these pruriceptive sub clusters.
Infection.
Staphylococcus aureus, a bacterial pathogen associated with itchy skin diseases, directly activates pruriceptor sensory neurons to drive itch. Skin exposure to
S. aureus causes robust itch and scratch-induced damage.
Spinal itch pathway After the pruriceptive primary afferent has been activated, the signal is transmitted from the skin into the spinal dorsal horn. In this area, a number of interneurons will either be inhibited or activated to promote activation of projection neurons, mediating the pruriceptive signal to the brain. The GRP-GRPR interneuron system has been found to be important for mediating both histaminergic and non-histaminergic itch, where the GRP neurons activate GRPR neurons to promote itch.
Neuropathic Neuropathic itch can originate at any point along the afferent pathway as a result of damage of the
nervous system. They could include diseases or disorders in the
central nervous system or
peripheral nervous system.
Neurogenic Neurogenic itch, which is itch induced centrally but with no neural damage, is mostly associated with increased accumulation of exogenous
opioids and possibly
synthetic opioids. NGF is known to up-regulate neuropeptides, especially
substance P. Substance P has been found to have an important role in inducing pain; however, there is no confirmation that substance P directly causes acute sensitization. Instead, substance P may contribute to itch by increasing
neuronal sensitization and may affect release of
mast cells, which contain many granules rich in histamine, during long-term interaction.
Central sensitization Noxious input to the
spinal cord is known to produce central sensitization, which consists of
allodynia, exaggeration of pain, and punctuate
hyperalgesia, extreme sensitivity to pain. Two types of mechanical hyperalgesia can occur: 1) touch that is normally painless in the uninjured surroundings of a cut or tear can trigger painful sensations (touch-evoked hyperalgesia), and 2) a slightly painful pin prick stimulation is perceived as more painful around a focused area of inflammation (punctuate hyperalgesia). Touch-evoked hyperalgesia requires continuous firing of primary afferent nociceptors, and punctuate
hyperalgesia does not require continuous firing which means it can persist for hours after a
trauma and can be stronger than normally experienced. In addition, it was found that patients with
neuropathic pain, histamine
ionophoresis resulted in a sensation of burning pain rather than itch, which would be induced in normal healthy patients. This shows that there is spinal hypersensitivity to
C-fiber input in
chronic pain. == Treatment ==