AI Article Synopsis

  • Spexin (SPX) is a neuropeptide involved in anxiety regulation, and its mRNA expression decreases in the hippocampus of stressed mice, while corticotropin-releasing factor (CRF) levels increase.
  • CRF, known for its role in depression and anxiety, reduces SPX mRNA levels through activation of corticotropin-releasing factor receptor 2 (CRFR2) but not receptor 1 (CRFR1), highlighting a specific signaling pathway.
  • The inhibition of SPX gene expression by CRF occurs at the promoter level in hippocampal cells, involving various signaling cascades like AC/cAMP/PKA and MEK/Erk, which may influence anxiety responses in the central nervous system

Article Abstract

Spexin (SPX) acts as a neuropeptide with pleiotropic functions that can participate in anxiety regulation. Corticotropin releasing factor (CRF) is widely expressed in brain tissues and associated with depression and anxiety and addiction. With the anxious mice under chronic unpredictable stress, we found SPX mRNA expression level in the hippocampus of the brain was significantly reduced, while local CRF mRNA expression level was increased. Furthermore, CRF injection in the hippocampus could also decrease SPX mRNA expression levels in hippocampus and other brain tissues, including pituitary and hypothalamus. With the primary mouse hippocampal cell model, CRF treatment could decrease SPX mRNA expression at hippocampal cell level and this inhibitory effect was mediated only by corticotropin releasing factor receptor 2 (CRFR2) but not corticotropin releasing factor receptor 1 (CRFR1). In HEK293 cells with CRFR2 over-expression, CRF could also inhibit SPX promoter activity coupling with AC/cAMP/PKA and MEK/Erk cascades. In addition, Epac was also involved with the CRF-repressed SPX promoter activity and cross-talked with MEK/Erk pathway. CRF could inhibit SPX gene expression in mouse hippocampus via transcriptional activation at the promoter level with coupling of AC/cAMP and MEK/Erk signaling, which will be relevant to the anxiety response mediated by SPX in central nervous system.

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http://dx.doi.org/10.1016/j.bbrc.2020.02.023DOI Listing

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