Unidirectional cross-activation of GRPR by MOR1D uncouples itch and analgesia induced by opioids

Cell. 2011 Oct 14;147(2):447-58. doi: 10.1016/j.cell.2011.08.043.

Abstract

Spinal opioid-induced itch, a prevalent side effect of pain management, has been proposed to result from pain inhibition. We now report that the μ-opioid receptor (MOR) isoform MOR1D is essential for morphine-induced scratching (MIS), whereas the isoform MOR1 is required only for morphine-induced analgesia (MIA). MOR1D heterodimerizes with gastrin-releasing peptide receptor (GRPR) in the spinal cord, relaying itch information. We show that morphine triggers internalization of both GRPR and MOR1D, whereas GRP specifically triggers GRPR internalization and morphine-independent scratching. Providing potential insight into opioid-induced itch prevention, we demonstrate that molecular and pharmacologic inhibition of PLCβ3 and IP3R3, downstream effectors of GRPR, specifically block MIS but not MIA. In addition, blocking MOR1D-GRPR association attenuates MIS but not MIA. Together, these data suggest that opioid-induced itch is an active process concomitant with but independent of opioid analgesia, occurring via the unidirectional cross-activation of GRPR signaling by MOR1D heterodimerization.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Analgesia*
  • Analgesics, Opioid / administration & dosage*
  • Animals
  • Mice
  • Mice, Knockout
  • Molecular Sequence Data
  • Morphine / administration & dosage*
  • Pain / drug therapy*
  • Pruritus / chemically induced*
  • Receptors, Bombesin / genetics
  • Receptors, Bombesin / metabolism*
  • Receptors, Opioid, mu / genetics
  • Receptors, Opioid, mu / metabolism*
  • Signal Transduction

Substances

  • Analgesics, Opioid
  • Receptors, Bombesin
  • Receptors, Opioid, mu
  • Morphine