Up-regulation of cutaneous α1 -adrenoceptors in complex regional pain syndrome type I

Pain Med. 2014 Nov;15(11):1945-56. doi: 10.1111/pme.12548. Epub 2014 Sep 12.

Abstract

Background: In a small radioligand-binding study of cutaneous α1 -adrenoceptors in complex regional pain syndrome (CRPS), signal intensity was greater in the CRPS-affected limb than in controls. However, it was not possible to localize heightened expression of α1 -adrenoceptors to nerves, sweat glands, blood vessels, or keratinocytes using this technique.

Methods: To explore this in the present study, skin biopsies were obtained from 31 patients with CRPS type I and 23 healthy controls of similar age and sex distribution. Expression of α1 -adrenoceptors on keratinocytes and on dermal blood vessels, sweat glands, and nerves was assessed using immunohistochemistry.

Results: α1 -Adrenoceptors were expressed more strongly in dermal nerve bundles and the epidermis both on the affected and contralateral unaffected side in patients than in controls (P<0.05). However, expression of α1 -adrenoceptors in sweat glands and blood vessels was similar in patients and controls. α1 -Adrenoceptor staining intensity in the CRPS-affected epidermis was associated with pain intensity (P < 0.05), but a similar trend for nerve bundles did not achieve statistical significance.

Discussion: Epidermal cells influence nociception by releasing ligands that act on sensory nerve fibers. Moreover, an increased expression of α1 -adrenoceptors on nociceptive afferents has been shown to aggravate neuropathic pain. Thus, the heightened expression of α1 -adrenoceptors in dermal nerves and epidermal cells might augment pain and neuroinflammatory disturbances after tissue injury in patients with CRPS type I.

Keywords: Complex Regional Pain Syndrome; Dermal Nerves; Epidermis; Immunohistochemistry; α1-Adrenoceptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biopsy
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Receptors, Adrenergic, alpha-1 / metabolism*
  • Reflex Sympathetic Dystrophy / metabolism*
  • Skin / metabolism*
  • Up-Regulation
  • Young Adult

Substances

  • Receptors, Adrenergic, alpha-1