MicroRNA-27a participates in the pathological process of depression in rats by regulating VEGFA

Jian Cui1, Cunqi Gong2, Baorui Cao2

  • 1Department of Psychiatry, Jining Psychiatric Hospital, Jining, Shandong 272051, P.R. China.

Insights

This study found that microRNA (miR)-27a is upregulated in rats with depression, while vascular endothelial growth factor A (VEGFA) is downregulated in both brain tissue and blood. miR-27a appears to regulate VEGFA, suggesting a role in depression pathology.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • Depression is a complex mental disorder with underlying molecular mechanisms that are not fully understood.
  • Vascular Endothelial Growth Factor A (VEGFA) plays a role in neurogenesis and vascularization, and its dysregulation has been implicated in depression.
  • MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression and are increasingly recognized for their involvement in psychiatric disorders.

Purpose of the Study:

  • To investigate the expression levels of VEGFA and miR-27a in the hippocampus and serum of a rat model of depression.
  • To elucidate the regulatory mechanism of miR-27a in the context of depression.
  • To explore the potential relationship between miR-27a and VEGFA in the pathophysiology of depression.

Main Methods:

  • Establishment of a rat model of depression using 14 types of stimuli.
  • Assessment of depression severity through body weight, syrup consumption, and open field tests.
  • Quantitative polymerase chain reaction (qPCR) for VEGFA mRNA and miR-27a expression.
  • Enzyme-linked immunosorbent assay (ELISA) for serum VEGFA protein.
  • Western blotting for hippocampal VEGFA protein.
  • Dual-luciferase reporter assay to confirm the interaction between miR-27a and VEGFA mRNA.

Main Results:

  • The depression model in rats was successfully established, exhibiting characteristic depression symptoms.
  • Rats with depression showed significantly lower expression of VEGFA mRNA and protein in both hippocampal tissues and peripheral blood compared to controls.
  • Levels of miR-27a were reduced in the hippocampus and peripheral blood of depressed rats.
  • A direct interaction was confirmed, where miR-27a binds to the 3'-untranslated region of VEGFA mRNA, thereby regulating its expression.

Conclusions:

  • The study demonstrates an upregulation of miR-27a and a downregulation of VEGFA (mRNA and protein) in the hippocampus and serum of rats with depression.
  • miR-27a may play a significant role in the pathological processes of depression by negatively regulating VEGFA expression.
  • These findings highlight a novel molecular pathway involving miR-27a and VEGFA in the development of depression.

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