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Quercetin Protects Blood-Brain Barrier Integrity via the PI3K/Akt/Erk Signaling Pathway in a Mouse Model of Meningitis Induced by . | LitMetric

AI Article Synopsis

  • This study investigates the effects of quercetin on brain inflammation and blood-brain barrier (BBB) integrity in a mouse model affected by infection.
  • Researchers found that infection caused significant brain inflammation and disrupted BBB integrity, while quercetin demonstrated anti-inflammatory and protective properties.
  • The results suggest that quercetin may help maintain BBB integrity through the activation of the PI3K/Akt/Erk signaling pathway, indicating its potential as a natural treatment for infections.

Article Abstract

() causes serious inflammation and meningitis in piglets. Quercetin has anti-inflammatory and anti-bacterial activities; however, whether quercetin can alleviate brain inflammation and provide protective effects during infection has not been studied. Here, we established a mouse model of infection in vivo and in vitro to investigate transcriptome changes in the mouse cerebrum and determine the protective effects of quercetin on brain inflammation and blood-brain barrier (BBB) integrity during infection. The results showed that induced brain inflammation, destroyed BBB integrity, and suppressed PI3K/Akt/Erk signaling-pathway activation in mice. Quercetin decreased the expression of inflammatory cytokines (, , , and ) and BBB-permeability marker genes (, , , and ), increased the expression of angiogenetic genes ( and ), reduced -induced tight junction disruption, and reactivated -induced suppression of the PI3K/Akt/Erk signaling pathway in vitro. Thus, we concluded that quercetin may protect BBB integrity via the PI3K/Akt/Erk signaling pathway during infection. This was the first attempt to explore the protective effects of quercetin on brain inflammation and BBB integrity in a -infected mouse model. Our findings indicated that quercetin is a promising natural agent for the prevention and treatment of infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11201931PMC
http://dx.doi.org/10.3390/biom14060696DOI Listing

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