The rapid antidepressant effect of acupuncture on two animal models of depression by inhibiting M1-Ach receptors regulates synaptic plasticity in the prefrontal cortex

Brain Res. 2024 Jan 1:1822:148609. doi: 10.1016/j.brainres.2023.148609. Epub 2023 Sep 30.

Abstract

Background: It is unclear whether acupuncture has a rapid antidepressant effect and what is the main mechanism.

Methods: In this study, forced swimming stress test (FST) in mice were divided into five groups: control group, acupuncture group, scopolamine group, arecoline group, and acupuncture + arecoline group. Chronic unpredictable mild stress (CUMS) model rats were divided into six groups: naïve (non-CUMS) group, CUMS group, acupuncture group, scopolamine group, arecoline group, and acupuncture + arecoline group. Twenty-four hours after the end of treatment, FST was conducted in mice and rats. The expression of M1-AchR, AMPA receptors (GluR1 and GluR2), BDNF, mTOR, p-mTOR, synapsin I, and PSD95 in the prefrontal cortex was determined by western blot. The spine density of neurons in the prefrontal cortex was detected by golgi staining.

Results: The results showed that acupuncture reduced the immobility time of FST in two depression models. Acupuncture inhibited the expression of M1-AchR and promoted the expression of GluR1, GluR2, BDNF, p-mTOR, synapsin I, PSD95, and increased the density of neuron dendritic spine in the prefrontal cortex.

Conclusions: The rapid antidepressant effect of acupuncture may be activating the "glutamate tide" - AMPA receptor activation - BDNF release - mTORC1 pathway activation through inhibiting the expression of M1-AchR in the prefrontal cortex, thereby increasing the expression of synaptic proteins and regulating synaptic plasticity.

Keywords: Acupuncture; Depression; M1-AchR; Prefrontal cortex; Synaptic plasticity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acupuncture Therapy*
  • Animals
  • Antidepressive Agents / metabolism
  • Antidepressive Agents / pharmacology
  • Arecoline / metabolism
  • Arecoline / pharmacology
  • Brain-Derived Neurotrophic Factor / metabolism
  • Depression* / metabolism
  • Depression* / therapy
  • Disease Models, Animal
  • Hippocampus / metabolism
  • Mice
  • Neuronal Plasticity
  • Prefrontal Cortex / metabolism
  • Rats
  • Scopolamine / pharmacology
  • Stress, Psychological / metabolism
  • Stress, Psychological / therapy
  • Synapsins / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • Synapsins
  • Arecoline
  • Antidepressive Agents
  • TOR Serine-Threonine Kinases
  • Scopolamine