Melatonin Reduces Mito‐Inflammation in Ischaemic Hippocampal HT22 Cells and Modulates the cGAS–STING Cytosolic DNA Sensing Pathway and FGF21 Release
2024

Melatonin Reduces Inflammation in Ischaemic Brain Cells

publication Evidence: high

Author Information

Author(s): Carloni Silvia, Nasoni Maria Gemma, Casabianca Anna, Orlandi Chiara, Capobianco Loredana, Iaconisi Giorgia Natalia, Cerioni Liana, Burattini Sabrina, Benedetti Serena, Reiter Russel J., Balduini Walter, Luchetti Francesca

Primary Institution: Department of Biomolecular Sciences University of Urbino Carlo Bo

Hypothesis

Does melatonin modulate mito-inflammation and FGF21 release in ischaemic hippocampal HT22 cells?

Conclusion

Melatonin effectively reduces mito-inflammation and modulates FGF-21 release in ischaemic brain injury.

Supporting Evidence

  • Melatonin reduced oxidative damage and preserved mitochondrial function in HT22 cells.
  • Melatonin decreased the release of mtDNA into the cytosol.
  • Melatonin modulated the cGAS–STING pathway and reduced inflammatory cytokine production.
  • FGF-21 release was increased by melatonin treatment in ischaemic conditions.

Takeaway

Melatonin helps protect brain cells from damage caused by lack of oxygen and sugar, making them healthier and less inflamed.

Methodology

HT22 cells were subjected to oxygen-glucose deprivation followed by reoxygenation, and the effects of melatonin on oxidative damage, mitochondrial function, and inflammatory responses were assessed.

Limitations

The study was conducted in vitro, which may not fully replicate in vivo conditions.

Statistical Information

P-Value

p<0.0001

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1111/jcmm.70285

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