Neurobiology of the trigeminal ganglion in comparison to the dorsal root ganglion.

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Date

2026-07

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Abstract

Abstract

The trigeminal ganglion (TG) represents the craniofacial counterpart of the dorsal root ganglion (DRG) in the peripheral nervous system (PNS). TG and DRG are clusters of cell bodies of highly specialized sensory neurons, with TG neurons innervating the head and face and DRG neurons innervating the body. TG and DRG neurons are essential for detecting various mechanical, thermal, and chemical stimuli and relaying these internal or external signals to the central nervous system (CNS). Despite sharing fundamental similarities, TG and DRG differ significantly in many aspects under pathophysiological states. This review provides a comparison between these 2 types of ganglia by highlighting their distinctions across anatomical locations, embryological origins, cellular compositions, gene expression profiles and molecular signatures, ratios of A/C fibers, connections with the CNS, sympathetic fiber sprouting, ectopic discharges, biophysical properties of ion channels, and neuron-glia interactions. These divergences may contribute to certain differences in intensities and responses to the same stimuli or treatments between TG- and DRG-mediated pain. Acknowledging their neurobiological distinctions underscores the importance of identifying potential pain targets within each system independently and developing targeted therapeutic strategies for craniofacial vs somatic pain.

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Circuit, Dorsal root ganglion, Fiber, Gene, Ion channels, Neuron, Pain, Satellite glial cell, Trigeminal ganglion

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Published Version (Please cite this version)

10.1097/j.pain.0000000000004062

Publication Info

Su, Shanchun, Minseok Kim, Wolfgang Liedtke and Yong Chen (2026). Neurobiology of the trigeminal ganglion in comparison to the dorsal root ganglion. Pain. 10.1097/j.pain.0000000000004062 Retrieved from https://hdl.handle.net/10161/35414.

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Scholars@Duke

Chen

Yong Chen

Associate Professor in Neurology

Dr. Yong Chen is an Associate Professor of Neurology at the Duke University School of Medicine.  He is also affiliated with Duke Anesthesiology-Center for Translational Pain Medicine (CTPM) and Duke-Pathology.

 

The Chen lab mainly studies sensory neurobiology of pain and itch, with a focus on TRP ion channels and neural circuits. The main objective of our lab is to identify molecular and cellular mechanisms underlying chronic pain and chronic-disease associated itch, using a combination of animal behavioral, genetic, molecular and cellular, advanced imaging, viral, and optogenetic approaches.  There are three major research areas in the lab: craniofacial pain, arthritis pain and joint function, and systemic-disease associated itch.


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