Cellular basis of itch sensation

Science. 2009 Sep 18;325(5947):1531-4. doi: 10.1126/science.1174868. Epub 2009 Aug 6.

Abstract

Itch and pain are two distinct sensations. Although our previous study suggested that gastrin-releasing peptide receptor (GRPR) is an itch-specific gene in the spinal cord, a long-standing question of whether there are separate neuronal pathways for itch and pain remains unsettled. We selectively ablated lamina I neurons expressing GRPR in the spinal cord of mice. These mice showed profound scratching deficits in response to all of the itching (pruritogenic) stimuli tested, irrespective of their histamine dependence. In contrast, pain behaviors were unaffected. Our data also suggest that GRPR+ neurons are different from the spinothalamic tract neurons that have been the focus of the debate. Together, the present study suggests that GRPR+ neurons constitute a long-sought labeled line for itch sensation in the spinal cord.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afferent Pathways / physiology
  • Animals
  • Behavior, Animal
  • Bombesin / pharmacology
  • Chronic Disease
  • Histamine
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / physiology*
  • Pain / physiopathology
  • Pruritus / physiopathology*
  • Receptors, Bombesin / genetics
  • Receptors, Bombesin / metabolism*
  • Ribosome Inactivating Proteins, Type 1 / pharmacology
  • Saporins
  • Sensation / physiology
  • Spinal Cord / cytology*
  • Spinothalamic Tracts / cytology
  • Spinothalamic Tracts / physiology

Substances

  • Receptors, Bombesin
  • Ribosome Inactivating Proteins, Type 1
  • Histamine
  • Saporins
  • Bombesin