4.3 Article

Aerobic exercise reverses the NF-κB/NLRP3 inflammasome/5-HT pathway by upregulating irisin to alleviate post-stroke depression

Journal

ANNALS OF TRANSLATIONAL MEDICINE
Volume 10, Issue 24, Pages -

Publisher

AME PUBLISHING COMPANY
DOI: 10.21037/atm-22-5443

Keywords

Post-stroke depression; aerobic exercise; irisin; nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3)

Funding

  1. General Project of Hunan Provincial Natural Fund [2020JJ4399]
  2. 2019 Hunan Provincial People's Hospital Benevolence Fund Project [RS201,907]

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In this study, aerobic exercise was found to have a protective effect on a mouse model of post-stroke depression (PSD), and it was discovered that aerobic exercise is involved in PSD through the serotonin (5-HT) signaling pathway and the protein irisin. Aerobic exercise inhibits the activation of the nuclear factor kappa B (NF-kappa B)/nucleotide-binding oligomerization domain--like receptor protein 3 (NLRP3) inflammasome, reduces mitochondrial damage, and alleviates PSD.
Background: Post-stroke depression (PSD) is one of the most common and serious sequelae of stroke. The pathogenesis of PSD involves both psychosocial and biological mechanisms, and aerobic exercise is a potential therapeutic target. We conducted an in-depth exploration of the protective mechanisms of aerobic exercise in a PSD mouse model. Methods: In this study, C57BL/6 mice were used as the research objects, and a PSD mouse model was established by combining middle cerebral artery occlusion and chronic unpredictable mild stimulation. Real-time quantitative polymerase chain reaction, enzyme-linked immunosorbent assays, adeno-associated virus microinjection technology, co-immunoprecipitation, fluorescence in-situ hybridization, and western blotting were performed. A moderate-load treadmill exercise was used for aerobic exercise intervention. The moderate-intensity aerobic exercise training method adopted 0 slopes and treadmill adaptation training for 5 days. We verified the effects of aerobic exercise on the nuclear factor kappa B (NF-kappa B)/nucleotide-binding oligomerization domain--like receptor protein 3 (NLRP3) inflammasome/5-hydroxytryptamine (5-HT) pathway. Results: Aerobic exercise effectively alleviated the neurological damage caused by PSD (P<0.01). The results from the PSD mouse model in vivo were consistent with those of the cell experiments. Moreover, overexpression of irisin improves depression-like behavior in PSD mice. We confirmed that aerobic exercise is involved in PSD through 5-HT, which inhibits NF-kappa B/NLRP3 inflammasome initiation through irisin and alleviates mitochondrial damage under stress by reducing calcium overload, thereby inhibiting NLRP3 inflammasome activation. Conclusions: Aerobic exercise reversed the NF-kappa B/NLRP3 inflammasome/5-HT pathway by upregulating irisin expression to alleviate PSD.

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