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Electroacupuncture ameliorates sleep deprivation-induced insomnia in mice by regulating the dopaminergic projections from VTA to NAc

Authors
 Weichao Pan  ;  Sijia Wang  ;  Ying Liu  ;  Shan Qin 3  ;  Feifei Ge  ;  Xiya Yuan  ;  Yuyang Bo  ;  Haoqing Tai  ;  Chengyong Liu  ;  Yu Fan  ;  Xiaoqiu Wang  ;  Hee Young Kim  ;  Wenzhong Wu  ;  Xiaowei Guan 
Citation
 EXPERIMENTAL NEUROLOGY, Vol.392 : 115351, 2025-10 
Journal Title
EXPERIMENTAL NEUROLOGY
ISSN
 0014-4886 
Issue Date
2025-10
MeSH
Acupuncture Points Animals Chemogenetics Chronic Disease / therapy Disease Models, Animal Dopaminergic Neurons / physiology Electroacupuncture* / methods Electroencephalography Male Mice Mice, Inbred C57BL Neural Pathways / physiopathology Nucleus Accumbens* / cytology Nucleus Accumbens* / physiopathology Sleep Deprivation* / complications Sleep Deprivation* / physiopathology Sleep Deprivation* / therapy Sleep Initiation and Maintenance Disorders* / etiology Sleep Initiation and Maintenance Disorders* / physiopathology Sleep Initiation and Maintenance Disorders* / therapy Sleep Stages / physiology Stereotaxic Techniques Ventral Tegmental Area* / cytology Ventral Tegmental Area* / physiopathology
Keywords
Dopaminergic pathway ; Electroacupuncture ; Nucleus accumbens ; Sleep deprivation ; Ventral tegmental area
Abstract
Background: The electroacupuncture (EA) has emerged as a potential therapeutic approach for the treatment of chronic insomnia, however, its underlying brain mechanism remain unclear.

Methods: Chronic sleep deprivation (CSD) mice models was established to investigate the effect of EA at acupoints of Yintang (EX-HN3), Shenmen (HT7), and Sanyinjiao (SP6) on CSD. With the methods of EEG/EMG recordings and chemogenetic manipulations, we explore the role of the dopaminergic projections from ventral tegmental area (VTA) to nucleus accumbens (NAc) in the therapeutic effects of EA on CSD-induced insomnia.

Results: We found that EA significantly alleviated CSD-induced insomnia, as indicated by an increased total sleep time and non-rapid eye movement (NREM) sleep during the dark period, along with attenuating the CSD-caused hyperactivity of VTA dopamine neurons in mice. Chemogenetic inhibition of the dopaminergic projections from VTA to NAc could restore the NREM sleep in CSD mice. Most importantly, the therapeutic effects of EA on CSD-induced insomnia was counteracted by activating the dopaminergic projections from VTA to NAc of mice.

Conclusion: These findings suggested that the therapeutic effects of EA at EX-HN3, HT7 and SP6 are achieved by targeting the dopaminergic projections from VTA to NAc, which could be therapeutic approach for chronic insomnia.
Full Text
https://www.sciencedirect.com/science/article/pii/S0014488625002158
DOI
10.1016/j.expneurol.2025.115351
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Physiology (생리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Hee Young(김희영) ORCID logo https://orcid.org/0000-0002-2495-9115
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/207204
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