2018
DOI: 10.1096/fj.201700908r
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Postovulatory aging causes the deterioration of porcine oocytes via induction of oxidative stress

Abstract: Negative effects of postovulatory aging on fertilization ability and subsequent embryo development have been reported in rodents; however, the molecular and cellular changes during this process have not been fully defined. Here, we used porcine oocytes, a model that is physiologically and developmentally similar to humans, to explore the molecular mechanisms that underlie how postovulatory aging affects oocyte quality and fertilization capacity. We found that postovulatory aging caused the morphologic change o… Show more

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Cited by 55 publications
(53 citation statements)
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References 33 publications
(39 reference statements)
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“…Excessive production of reactive oxygen species has detrimental effects on cellular metabolism and other physiological activities. Studies have found that excessive levels of ROS can cause deterioration in oocytes quality and disrupts the meiotic process (Chaube et al ; Miao et al ). After exposure to IBP, we assessed the level of oxidative stress in the cytoplasm of oocytes.…”
Section: Discussionmentioning
confidence: 99%
“…Excessive production of reactive oxygen species has detrimental effects on cellular metabolism and other physiological activities. Studies have found that excessive levels of ROS can cause deterioration in oocytes quality and disrupts the meiotic process (Chaube et al ; Miao et al ). After exposure to IBP, we assessed the level of oxidative stress in the cytoplasm of oocytes.…”
Section: Discussionmentioning
confidence: 99%
“…Very little information is available about antiaging effectors in oocytes, and the mechanism for rescuing or preventing oocyte aging Several studies have investigated the degradation of oocyte quality with aging time. Embryos from oocytes aged for more than 48 hr rarely develop into blastocysts (Lee et al, 2014;Miao et al, 2018;Němeček, Dvořáková, Heroutová, Chmelíková, & Sedmíková, 2017). Although aging for 24 hr also decreases oocyte competence, this effect can be recovered by antiaging systems (Lee et al, 2014;Ma, Zhang, Zhang, Han, & Rui, 2015).…”
Section: Discussionmentioning
confidence: 99%
“…With the treatment of increasing doses of the inhibitor, the oocytes exhibited a significantly decreased rate of polar body extrusion with poor expansion of cumulus cells, suggesting that inhibition of Eg5 perturbs the meiotic progression. Previous studies by us and others have shown that oocyte meiotic arrest is largely caused by the defective spindle assembly and chromosome alignment [ 31 , 36 , 37 ]. Additionally, Eg5 has been found to sort and push microtubules apart to drive the separation of spindle poles [ 12 ], and loss of Eg5 leads to cell cycle arrest and defective centrosome separation resulting in the development of monopolar spindles [ 38 ].…”
Section: Discussionmentioning
confidence: 99%