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These complexes are delivered to ferritin via the ferric iron molecular chaperone poly(C)-binding protein 1 (PCBP1), exacerbating labile iron availability and ferroptosis progression

This mechanism is also supported by other studies

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These techniques involve the identification and quantification of protein carbonyls and other oxidative markers, providing valuable insights into the extent of oxidative damage in spermatozoa

The high rate of oxygen consumption and the presence of redox active metals such as Fe ++ and Cu ++ account for an increased generation of reactive oxygen/nitrogen metabolites