2018
DOI: 10.1002/mrd.23052
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Melatonin supplementation during prolonged in vitro maturation improves the quality and development of poor‐quality porcine oocytes via anti‐oxidative and anti‐apoptotic effects

Abstract: Poor-quality oocytes (those with 1-2 layers of cumulus cells) typically possess low meiotic competence and development. Prolonging the duration of in vitro maturation (IVM; 52 hr) can enhance the maturation rate of poor-quality oocytes, but it does not improve subsequent embryonic development. This likely reflects the increased reactive oxygen species (ROS) production and apoptosis seen in these oocytes compared with the non-prolonged IVM (44 hr) group. Melatonin is a free radical scavenger, anti-oxidant and a… Show more

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Cited by 38 publications
(29 citation statements)
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“…Benzo(a)pyrene leads to oocyte meiotic failure, which can be recovered by melatonin supplementation through repressing ROS level in the porcine [34]. Melatonin combined with prolonged IVM enhances development of poor-quality oocytes through decreasing ROS generation in pigs [35]. The combination of GSH with L-cysteine decreases ROS production, which can be used to enhance blastocyst quality in IVC systems in pigs [36].…”
Section: Discussionmentioning
confidence: 99%
“…Benzo(a)pyrene leads to oocyte meiotic failure, which can be recovered by melatonin supplementation through repressing ROS level in the porcine [34]. Melatonin combined with prolonged IVM enhances development of poor-quality oocytes through decreasing ROS generation in pigs [35]. The combination of GSH with L-cysteine decreases ROS production, which can be used to enhance blastocyst quality in IVC systems in pigs [36].…”
Section: Discussionmentioning
confidence: 99%
“…The addition melatonin to the culture medium wound detoxifies ROS, thereby reducing oxidative damage so as to protect the oocytes and granulosa cells. Reducing oxidative stress and apoptosis of oocytes and promoting mitochondrial function via melatonin treatment have been shown to improve oocyte maturation, fertilization rate, and rate of blastocyst formation (blastocyst cell count) [51][52][53]. Furthermore, the effect of oxidative stress induced by substances that generate ROS, such as bisphenol A (BPA) and aflatoxin B1 (AFB1), is reduced when melatonin is added to the culture medium [54,55].…”
Section: Oocyte Maturation Embryo Development and Melatoninmentioning
confidence: 99%
“…While some reports have examined these intracellular processes of melatonin in oocytes [62][63][64][65], the details remain unclear. It has been reported that melatonin controls the expression of genes related to oocyte maturation including mitochondrial function [53,60,66,67], antioxidative enzymes [53,59,67,68], apoptosis [52,[65][66][67][68][69], cumulus cell expansion [51,61,70], and oocyte maturation factors [61,67]. Furthermore, epigenetic mechanisms such as DNA methylation and histone acetylation have also been reported [59,66,71].…”
Section: Oocyte Maturation Embryo Development and Melatoninmentioning
confidence: 99%
“…Additional variables associated with embryo cryosurvival are presented on Table 3. Thus, some strategies can be used to increase the cryotolerance of IVP embryos, such as culture under a low oxygen atmosphere system to minimize oxidative stress, addition of antioxidants to the culture medium, and the use of apoptosis inhibitors (Lin et al, 2018;Pero et al, 2018). As already mentioned, excessive lipid droplets accumulation of IVP embryos during development, especially of embryos cultured in serum-supplemented medium, is commonly associated with reduced cryosurvival and lower pregnancy rate (Rizos et al, 2008;Sudano et al, 2011).…”
Section: An Embryo-focused Approach To Improve Cryosurvivalmentioning
confidence: 99%