Thalamic CGRP neurons define a spinothalamic pathway for affective pain

S Sukjae J. Kang (Peptide Biology Laboratory, The Salk Institute for Biological Studies) S Shijia Liu (Peptide Biology Laboratory, The Salk Institute for Biological Studies) J Jong-Hyun Kim (Peptide Biology Laboratory, The Salk Institute for Biological Studies) D Dong-Il Kim (Peptide Biology Laboratory, The Salk Institute for Biological Studies) T Tae Gyu Oh (Gene Expression Laboratory, The Salk Institute for Biological Studies) J Jiahang Peng (Peptide Biology Laboratory, The Salk Institute for Biological Studies) M Mao Ye K Kuo-Fen Lee (Peptide Biology Laboratory, The Salk Institute for Biological Studies) R Ronald M. Evans M Martyn Goulding (Molecular Neurobiology Laboratory, The Salk Institute for Biological Studies) S Sung Han (Peptide Biology Laboratory, The Salk Institute for Biological Studies)

Abstract

Pain is both a sensory and emotional experience caused by various harmful stimuli. While numerous studies have explored peripheral and central pain mechanisms, the specific neural circuits linking the spinal cord to the brain remain poorly defined. In this study, we demonstrate the involvement of calcitonin gene-related peptide (CGRP)-positive neurons in the parvicellular part of the subparafascicular nucleus (SPFp) in pain. Tracing revealed that CGRP neurons in the SPFp (CGRP SPFp ) receive projections from the dorsal horn. Increased calcium activity was observed in CGRP SPFp neurons during mechanical, thermal, and inflammatory stimuli. Genetic silencing of these neurons resulted in reduced pain responses in animals. Furthermore, optogenetic activation of CGRP SPFp neurons induced aversive memory but did not alter mechanical or thermal pain thresholds. This study reveals a distinct neural circuit involving CGRP SPFp neurons that mediates pain, which differs from CGRP neurons in the parabrachial nucleus. Understanding these circuits could lead to better pain treatments with fewer side effects.

Article Details

Volume / Issue Vol. 122, Issue 28
Published July 15, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (11)

S

Sukjae J. Kang

Peptide Biology Laboratory, The Salk Institute for Biological Studies

S

Shijia Liu

Peptide Biology Laboratory, The Salk Institute for Biological Studies

J

Jong-Hyun Kim

Peptide Biology Laboratory, The Salk Institute for Biological Studies

D

Dong-Il Kim

Peptide Biology Laboratory, The Salk Institute for Biological Studies

T

Tae Gyu Oh

Gene Expression Laboratory, The Salk Institute for Biological Studies

J

Jiahang Peng

Peptide Biology Laboratory, The Salk Institute for Biological Studies

M

Mao Ye

K

Kuo-Fen Lee

Peptide Biology Laboratory, The Salk Institute for Biological Studies

R

Ronald M. Evans

M

Martyn Goulding

Molecular Neurobiology Laboratory, The Salk Institute for Biological Studies

S

Sung Han

Peptide Biology Laboratory, The Salk Institute for Biological Studies