Du-moxibustion ameliorates depression-like behavior and neuroinflammation in chronic unpredictable mild stress-induced mice

J Affect Disord. 2024 Aug 1:358:211-221. doi: 10.1016/j.jad.2024.05.025. Epub 2024 May 3.

Abstract

Background: Neuroinflammation is involved in the advancement of depression. Du-moxibustion can treat depression. Here, we explored whether Du-moxibustion could alleviate neuroglia-associated neuro-inflammatory process in chronic unpredictable mild stress (CUMS) mice.

Methods: C57BL/6J mice were distributed into five groups. Except for the CON group, other four groups underwent CUMS for four consecutive weeks, and Du-moxibustion was given simultaneously after modeling. Behavioral tests were then carried out. Additionally, Western blot was conducted to measure the relative expression levels of high-mobility group box 1 (HMGB1), toll-like receptor 4 (TLR4), myeloid differentiation factor 88 (MyD88), and nuclear factor-kappa B (NF-κB). Immunofluorescence was employed to evaluate the positive cells of ionized calcium binding adapter molecule 1 (Iba-1) and glial fibrillary acidic protein (GFAP). Furthermore, interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) were analyzed using an ELISA assay.

Results: We found that CUMS induced depression-like behaviors, such as reduced sucrose preference ratio, decreased locomotor and exploratory activity, decreased the time in open arms and prolonged immobility. Furthermore, versus the CON group, the expression of HMGB1, TLR4, MyD88, NF-κB, positive cells of Iba-1, IL-1β and TNF-α were increased but positive cells of GFAP were decreased in CUMS group. However, the detrimental effects were ameliorated by treatment with CUMS+FLU and CUMS+DM.

Limitations: A shortage of this study is that only CUMS model of depression were used, while other depression model were not included.

Conclusions: Du-moxibustion alleviates depression-like behaviors in CUMS mice mainly by reducing neuroinflammation, which offers novel insights into the potential treatment of depression.

Keywords: Astrocyte; Depression; Du-moxibustion; HMGB1/TLR4/NF-κB signaling pathway; Microglia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Depression* / drug therapy
  • Disease Models, Animal*
  • HMGB1 Protein* / metabolism
  • Interleukin-1beta / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Moxibustion*
  • Myeloid Differentiation Factor 88* / metabolism
  • NF-kappa B / metabolism
  • Neuroinflammatory Diseases* / drug therapy
  • Stress, Psychological* / complications
  • Toll-Like Receptor 4 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • HMGB1 Protein
  • Myeloid Differentiation Factor 88
  • Toll-Like Receptor 4
  • Tlr4 protein, mouse
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Interleukin-1beta
  • HMGB1 protein, mouse
  • Myd88 protein, mouse