Kang Sukjae J, Liu Shijia, Kim Jong-Hyun, Kim Dong-Il, Oh Tae Gyu, Peng Jiahang, Ye Mao, Lee Kuo-Fen, Evans Ronald M, Goulding Martyn, Han Sung
Peptide Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Gene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 2025 Jul 15;122(28):e2505889122. doi: 10.1073/pnas.2505889122. Epub 2025 Jul 9.
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) receive projections from the dorsal horn. Increased calcium activity was observed in CGRP neurons during mechanical, thermal, and inflammatory stimuli. Genetic silencing of these neurons resulted in reduced pain responses in animals. Furthermore, optogenetic activation of CGRP neurons induced aversive memory but did not alter mechanical or thermal pain thresholds. This study reveals a distinct neural circuit involving CGRP 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.
疼痛是由各种有害刺激引起的一种感觉和情感体验。虽然众多研究已探究了外周和中枢疼痛机制,但连接脊髓与大脑的特定神经回路仍未明确界定。在本研究中,我们证明了束旁核小细胞部(SPFp)中降钙素基因相关肽(CGRP)阳性神经元参与疼痛过程。追踪显示,SPFp中的CGRP神经元(CGRP)接收来自背角的投射。在机械、热和炎症刺激期间,观察到CGRP神经元中钙活性增加。这些神经元的基因沉默导致动物疼痛反应减轻。此外,CGRP神经元的光遗传学激活诱导了厌恶记忆,但未改变机械或热痛阈值。本研究揭示了一个涉及CGRP神经元的独特神经回路,该回路介导疼痛,这与臂旁核中的CGRP神经元不同。了解这些回路可能会带来副作用更少的更好的疼痛治疗方法。