4.4 Article

Somatostatin Neurons from Periaqueductal Gray to Medulla Facilitate Neuropathic Pain in Male Mice

Journal

JOURNAL OF PAIN
Volume 24, Issue 6, Pages 1020-1029

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.jpain.2023.01.002

Keywords

Chronic pain; neuropathic pain; periaqueductal gray; rostral ventromedial medulla neural mechanism

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This study reveals the contribution of somatostatin neurons within the PAG-RVM projections to descending pain facilitation in neuropathic pain and suggests their potential as a therapeutic target. The somatostatin-expressing glutamatergic neurons in the PAG form direct excitatory connections with RVM neurons, and inhibition of this projection alleviates hypersensitivity while activation enhances it.
Projections from the periaqueductal gray (PAG) to the rostral ventromedial medulla (RVM) are known to engage in descending pain modulation, but how the neural substrates of the PAG-RVM projections contribute to neuropathic pain remains largely unknown. In this study, we showed somatostatin-expressing glutamatergic neurons in the lateral/ventrolateral PAG that facilitate mechanical and thermal hypersensitivity in a mouse model of chemotherapy-induced neuropathic pain. We found that these neurons form direct excitatory connections with neurons in the RVM region. Inhibition of this PAG-RVM projection alleviates mechanical and thermal hypersensitivity associated with neuropathy, whereas its activation enhances hypersensitivity in the mice. Thus, our findings revealed that somatostatin neurons within the PAG-RVM axial are crucial for descending pain facilitation and can potentially be exploited as a useful therapeutic target for neuropathic pain.Perspective: We report the profound contribution of somatostatin neurons within the PAG-RVM projections to descending pain facilitation underlying neuropathic pain. These results may help to develop central therapeutic strategies for neuropathic pain.(c) 2023 The Author(s). Published by Elsevier Inc. on behalf of United States Association for the Study of Pain, Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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