J Intern Med 248 : 223229
Brandsch, C
1) include (1) impaired chromosome integrity due to increased DNA damage (e.g., DNA double-strand breaks) [21], (2) weakened chromosome cohesion during chromosome segregation, causing a decrease in the level of chromosomal adhesin subunits, making oocytes susceptible to premature sister chromatid segregation in homologous chromosomes [22, 23], (3) dysfunction of spindle assembly checkpoints, which interferes with chromosome segregation, leading to premature chromosome segregation and chromosome mislocalisation [24], (4) meiotic recombination errors [25], and (5) telomere shortening leading to impaired chromosome integrity [25]
Similarly, the released thiol compounds from glutathione upon entering the cell might react with the thiol groups on other proteins such as Kelch-like ECH-associated protein 1, which may enhance translocation of nuclear factors (erythroid-derived 2)-like 2 (NRF2) into the nuclei and expression of antioxidant enzymes
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