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March 26, 2026Molecular Pain2 citationsOpen Access

EXPRESS: The enhanced analgesic effects of electroacupuncture and repetitive transcranial magnetic stimulation on visceral pain via ventral lateral septal nucleus

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RWRui-Xia WengYGYuan GaoCZChen-Hao Zhang

Key Points

  • To explore the neural mechanisms by which electroacupuncture and repetitive transcranial magnetic stimulation alleviate visceral pain.
  • Identified the lateral septal nucleus (LSV) role in visceral pain modulation using a mouse model.
  • Measured c-Fos expression in LSV following visceral nociceptive stimulation.
  • Conducted optogenetic inhibition and activation of glutamatergic neurons in LSV to assess pain behaviors.
  • Evaluated the effects of EA and rTMS on pain behaviors and glutamate/cannabinoid dynamics.
  • Visceral nociceptive stimulation increased c-Fos expression in LSV glutamatergic neurons.
  • Optogenetic inhibition of these neurons reduced visceral pain, while activation worsened pain behaviors.
  • EA and rTMS reduced c-Fos expression and alleviated pain, with combined treatment being most effective.
  • Fiber photometry indicated decreased glutamate release and increased cannabinoid signaling following EA and rTMS.

Abstract

Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder characterized primarily by chronic visceral pain, with a complex pathogenesis and limited efficacy of current therapeutic interventions. Growing evidence indicates that electroacupuncture (EA) and repetitive transcranial magnetic stimulation (rTMS) exert significant analgesic effects on visceral pain. However, the underlying neural circuit mechanisms remain poorly understood. In this study, the ventral part of the lateral septal nucleus (LSV) was identified as a critical brain region mediating the analgesic effects of EA and rTMS in a mouse model of visceral pain. Visceral nociceptive stimulation significantly increased c-Fos expression in the LSV, predominantly within glutamatergic neurons. Optogenetic inhibition of LSV glutamatergic neurons attenuated visceral pain, whereas their activation exacerbated pain-related behaviors. Both EA and rTMS individually reduced visceral pain-induced c-Fos expression and alleviated pain behaviors, with the combined EA+rTMS treatment producing a more pronounced analgesic effect than either treatment alone. Moreover, fiber photometry recordings demonstrated that EA and rTMS decreased glutamate release and concurrently increased cannabinoid signaling in the LSV, suggesting that these interventions modulate neurotransmitter dynamics to regulate neuronal excitability. In summary, our findings highlight the pivotal role of LSV glutamatergic neurons in the modulation of visceral pain. EA and rTMS exert their therapeutic effects by regulating glutamate and cannabinoid release within this circuit. These insights provide a foundation for developing targeted neuromodulatory strategies for the treatment of chronic visceral pain.

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Cite This Study

Weng et al. (2026) studied this question.

synapsesocial.com/papers/69c4cd12fdc3bde448918f5fhttps://doi.org/10.1177/17448069261428970
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