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During BPD progression, hyperoxia exposure activates necroptotic pathways through multiple mechanisms

erinaceus alone resulted in only a slight decrease in SQSTM/p62 protein expression, but after the use of the AhR antagonist, the expression significantly increased

(L-N) Western blot analysis and quantitative assessment of MMP-2 and MMP-9 protein expression levels in each group

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In our recent study, in addition to elucidating the pathogenic mechanism of FUS-associated ALS in both Drosophila and animal systems, we found that overexpression of GstO2, a Drosophila homolog of human GSTO1, reduces cytoplasmic FUS aggregates and attenuates neurodegenerative phenotypes, including mitochondrial dysfunction and neuronal toxicity 148

Catalase's capacity to lower oxidative stress and inflammation shows its potential as a therapeutic agent in the treatment of CAP, which might lead to better clinical results and reduced disease severity [95, 96]