Upregulation of NR2A in Glutamatergic VTA Neurons Contributes to Chronic Visceral Pain in Male Mice.
10.1007/s12264-025-01402-7
- Author:
Meng-Ge LI
1
;
Shu-Ting QU
2
;
Yang YU
3
;
Zhenhua XU
1
;
Fu-Chao ZHANG
3
;
Yong-Chang LI
4
;
Rong GAO
5
;
Guang-Yin XU
6
Author Information
1. Center of Translational Medicine, The Zhangjiagang Affiliated Hospital of Soochow University, Zhangjiagang, 215600, China.
2. Department of Gastroenterology, Suzhou Dushu Lake Hospital, The Forth Affiliated Hospital of Soochow University, Suzhou, 215123, China.
3. Jiangsu Key Laboratory of Neuropsychiatric Diseases and Institute of Neuroscience, Soochow University, Suzhou, 215123, China.
4. Center of Translational Medicine, The Zhangjiagang Affiliated Hospital of Soochow University, Zhangjiagang, 215600, China. yongchangli@suda.edu.cn.
5. Center of Translational Medicine, The Zhangjiagang Affiliated Hospital of Soochow University, Zhangjiagang, 215600, China. gaorong1234@suda.edu.cn.
6. Jiangsu Key Laboratory of Neuropsychiatric Diseases and Institute of Neuroscience, Soochow University, Suzhou, 215123, China. guangyinxu@suda.edu.cn.
- Publication Type:Journal Article
- Keywords:
Chronic visceral pain;
Glutamatergic neurons;
Irritable bowel syndrome;
NMDA receptor 2A subunit;
Ventral tegmental area
- MeSH:
Animals;
Male;
Visceral Pain/metabolism*;
Up-Regulation/physiology*;
Ventral Tegmental Area/metabolism*;
Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors*;
Neurons/drug effects*;
Mice, Inbred C57BL;
Mice;
Proto-Oncogene Proteins c-fos/metabolism*;
Chronic Pain/metabolism*;
Glutamic Acid/metabolism*
- From:
Neuroscience Bulletin
2025;41(12):2113-2126
- CountryChina
- Language:English
-
Abstract:
Chronic visceral pain is a persistent and debilitating condition arising from dysfunction or sensitization of the visceral organs and their associated nervous pathways. Increasing evidence suggests that imbalances in central nervous system function play an essential role in the progression of visceral pain, but the exact mechanisms underlying the neural circuitry and molecular targets remain largely unexplored. In the present study, the ventral tegmental area (VTA) was shown to mediate visceral pain in mice. Visceral pain stimulation increased c-Fos expression and Ca2+ activity of glutamatergic VTA neurons, and optogenetic modulation of glutamatergic VTA neurons altered visceral pain. In particular, the upregulation of NMDA receptor 2A (NR2A) subunits within the VTA resulted in visceral pain in mice. Administration of a selective NR2A inhibitor decreased the number of visceral pain-induced c-Fos positive neurons and attenuated visceral pain. Pharmacology combined with chemogenetics further demonstrated that glutamatergic VTA neurons regulated visceral pain behaviors based on NR2A. In summary, our findings demonstrated that the upregulation of NR2A in glutamatergic VTA neurons plays a critical role in visceral pain. These insights provide a foundation for further comprehension of the neural circuits and molecular targets involved in chronic visceral pain and may pave the way for targeted therapies in chronic visceral pain.
