A subpopulation of projections from the parabrachial nucleus to the central amygdala mediates itch

  • Sci Rep. 2025 Jul 21;15(1):26432. doi: 10.1038/s41598-025-08612-z.
Darya Pavlenko  1 Hirotake Ishida  1 Anika Markan  1 Tasuku Akiyama  2
Affiliations
  • 1. Dr. Phillip Frost Department of Dermatology & Cutaneous Surgery and Miami Itch Center, University of Miami Miller School of Medicine, 1600 NW 10th Ave., RMSB2063, Miami, FL, USA.
  • 2. Dr. Phillip Frost Department of Dermatology & Cutaneous Surgery and Miami Itch Center, University of Miami Miller School of Medicine, 1600 NW 10th Ave., RMSB2063, Miami, FL, USA. [email protected].
Abstract

The parabrachial nucleus (PBN) plays a crucial role in transmitting itch and affective pain signals to the brain regions such as the central amygdala (CeA). While CGRP+ PBN neurons have been implicated in itch processing, the specific projections involved remain unclear. This study aimed to determine the proportion of itch-responsive PBN-CeA projections that express CGRP and to assess their functional role in itch and anxiety behaviors in mice. Using the Targeted Recombination in Active Populations system, we labeled itch-responsive PBN neurons with serotonin. Retrograde tracing revealed that approximately half of serotonin-responsive PBN neurons projecting to the CeA are CGRP+. Optogenetic stimulation of these PBN-CeA neurons elicited scratching behavior but did not enhance pruritogen-induced scratching or affect anxiety-like behaviors. In a mouse model of chronic itch, the inhibition of PBN-CeA neurons significantly reduced spontaneous scratching without impacting anxiety-like behaviors. These findings suggest that serotonin-responsive PBN-CeA neurons include both CGRP+ and non-CGRP+ populations and selectively mediate itch signaling.

Keywords
CGRP; Optogenetics; Pain; Pruritus; Scratching.
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