Scratching behavior does not necessarily correlate with epidermal nerve fiber sprouting or inflammatory cell infiltration

J Dermatol Sci. 2010 May;58(2):130-5. doi: 10.1016/j.jdermsci.2010.03.007. Epub 2010 Mar 19.

Abstract

Background: Increased sprouting of epidermal nerve fibers of lesional skin are thought to be associated with persistent pruritus in chronic inflammatory dermatitis such as atopic dermatitis as supported by a murine study using tacrolimus (or FK506: FK) which was shown to inhibit both epidermal sprouting of nerves and scratching behavior or by immunohistochemical observations of lesional skin in the patients with atopic dermatitis or prurigo, etc.

Objectives: To examine a mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2 (MEK1/2) inhibitor (CX-659S: CX) for a possible anti-pruritic property in vivo since some MEK1/2 inhibitors have been reported to inhibit neurite growth in vitro.

Methods: CX, FK and corticosteroids (betamethasone valerate: BV) were topically applied on inflamed skin in a mouse model of chronic dermatitis using repetitive hapten painting to examine anti-pruritic property and anti-inflammatory effects. Scratching behaviors were assessed using MicroAct automatic measuring system, and epidermal sprouting of nerves and skin inflammation was assessed histologically.

Results: FK significantly decrease scratching behavior, but CX and BV failed to do so despite of their ability to significantly inhibit epidermal nerve fiber sprouting and skin inflammation, respectively. In addition, CX+BV mixture synergistically inhibited epidermal nerve fiber sprouting and skin inflammation even more potently than FK without decreasing scratching behavior.

Conclusions: These findings suggest that the scratching behavior does not necessarily correlate with epidermal nerve fiber sprouting or inflammatory cell infiltration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Disease Models, Animal
  • Epidermis / innervation*
  • Epidermis / pathology*
  • Female
  • Haptens / chemistry
  • Inflammation*
  • MAP Kinase Kinase 1 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Neurites / metabolism
  • Pruritus / drug therapy
  • Pruritus / pathology
  • Skin / pathology
  • Uracil / analogs & derivatives
  • Uracil / pharmacology
  • Wound Healing

Substances

  • Anti-Inflammatory Agents
  • Haptens
  • Uracil
  • MAP Kinase Kinase 1
  • CX 659S