Synergistic effects of citicoline and silymarin nanomicelles in restraint stress-exposed mice

Behav Brain Res. 2024 Apr 27:464:114929. doi: 10.1016/j.bbr.2024.114929. Epub 2024 Feb 29.

Abstract

This study evaluated the effects of citicoline and silymarin nanomicelles (SMnm) in repeated restraint stress (RRS).

Method: Mice were exposed to RRS for four consecutive days, 2 hrs. daily. On day 5 of the study, SMnm (25 and 50 mg/kg, i.p.) and citicoline (25 and 75 mg/kg), and a combination of them (25 mg/kg, i.p.) were initiated. On day 18, anxiety-like behavior, behavioral despair, and exploratory behavior were evaluated. The prefrontal cortex (PFC) and the hippocampus were dissected measuring brain-derived neurotrophic factor (BDNF), cAMP response element-binding protein (CREB), and tumor necrosis factor-alpha (TNF-α) through Western Blot and ELISA, respectively.

Results: In RR-exposed mice, anxiety-like behavior in the elevated plus maze (EPM) was enhanced by reductions in open arm time (OAT%) P < 0.001, and open arm entry (OAE%) P < 0.001. In the forced swimming test (FST), the immobility increased P < 0.001 while the swimming and climbing reduced P < 0.001. In the open field test (OFT), general motor activity was raised P < 0.05. Further, body weights reduced P < 0.001, and tissue BDNF and pCREB expressions decreased P < 0.001 while TNF-α increased P < 0.001. Conversely, SMnm, citicoline and their combination could reduce anxiety-like behavior P < 0.001. The combination group reduced the depressive-like behaviors P < 0.001. Moreover, body weights were restored P < 0.001. Besides, BDNF and pCREB expressions increased while TNF-α reduced, P < 0.001.

Conclusion: The combination synergistically improved emotion-like behaviors, alleviating the inflammation and upregulating the hippocampal BDNF-mediated CREB signaling pathway.

Keywords: BDNF; CREB; Citicoline; Restraint stress; Silymarin nanomicelles; TNF-α.

MeSH terms

  • Animals
  • Antidepressive Agents* / pharmacology
  • Body Weight
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cytidine Diphosphate Choline / metabolism
  • Cytidine Diphosphate Choline / pharmacology
  • Depression / metabolism
  • Hippocampus / metabolism
  • Mice
  • Silymarin* / metabolism
  • Silymarin* / pharmacology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antidepressive Agents
  • Brain-Derived Neurotrophic Factor
  • Cytidine Diphosphate Choline
  • Silymarin
  • Tumor Necrosis Factor-alpha