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Published on: July 30, 2016
Modulation of Apoptosis and Autophagy by Melatonin in Juglone-Exposed Bovine Oocytes
Marwa El-Sheikh1, Ahmed Atef Mesalam2, Seon-Min Kang3
1Department of Microbial Biotechnology, Biotechnology Research Institute, National Research Centre (NRC), Dokki, Cairo 12622, Egypt.
Abstract:
Melatonin, an antioxidant hormone secreted by the pineal gland, has been recognized as a regulator for numerous biological events. The deleterious effects of juglone, a polyphenolic extract of walnut trees, on embryo development has been previously reported. In the current study, we aimed to display the impact of melatonin administrated during in vitro oocyte maturation (IVM) on juglone-treated oocytes. Thus, in vitro matured oocytes were collected after 24 h post incubation with juglone in the presence or absence of melatonin. Reactive oxygen species (ROS), glutathione (GSH) content, mitochondrial distribution, and the relative abundance of mRNA transcription levels were assessed in oocytes, in addition, oocytes were in vitro fertilized to check the competency levels of oocytes to generate embryos. We found that administration of melatonin during the maturation of oocytes under juglone stress significantly improved the cleavage rate, 8-16 cell-stage embryos and day-8 blastocysts when compared to the sole juglone treatment. In addition, the fluorescence intensity of ROS increased, whereas the GSH decreased in juglone-treated oocytes compared to melatonin-juglone co-treated and untreated ones. Additionally, a significant increase in the mitochondrial aberrant pattern, the pattern that was normalized following melatonin supplementation, was observed following juglone administration. The mRNA analysis using RT-qPCR revealed a significant upregulation of autophagy and oxidative-stress-specific markers in the juglone-treated group compared to the co-treatment and control. In conclusion, the study reveals, for the first time, a protective effect of melatonin against the oxidative stress initiated following juglone treatment during the in vitro maturation of oocytes.
Insights
Melatonin protects oocytes from juglone-induced oxidative stress during in vitro maturation. This antioxidant hormone improved embryo development and normalized mitochondrial function in treated oocytes.
Area of Science:
- Reproductive Biology
- Endocrinology
- Toxicology
Background:
- Melatonin, a pineal gland hormone, regulates biological events and possesses antioxidant properties.
- Juglone, a walnut extract, has demonstrated detrimental effects on embryo development.
- Oxidative stress is a critical factor impacting oocyte quality and developmental potential.
Purpose of the Study:
- To investigate the protective effects of melatonin on oocytes during in vitro maturation (IVM) when exposed to juglone.
- To assess the impact of melatonin on oxidative stress markers, mitochondrial function, and developmental competence in juglone-treated oocytes.
Main Methods:
- Oocytes were matured in vitro with juglone, with or without melatonin supplementation.
- Assessed reactive oxygen species (ROS), glutathione (GSH) levels, mitochondrial distribution, and mRNA expression.
- Evaluated oocyte developmental potential through in vitro fertilization and subsequent embryo development assessment.
Main Results:
- Melatonin supplementation significantly improved oocyte cleavage rates and the formation of 8-16 cell-stage embryos and day-8 blastocysts compared to juglone alone.
- Juglone treatment increased ROS and decreased GSH, while melatonin co-treatment normalized these levels.
- Juglone induced aberrant mitochondrial patterns, which were restored by melatonin.
- Autophagy and oxidative stress markers were upregulated by juglone, but normalized with melatonin co-treatment.
Conclusions:
- Melatonin demonstrates a protective effect against juglone-induced oxidative stress during IVM.
- Melatonin improves oocyte quality and developmental competence under toxic conditions.
- This study highlights melatonin's potential therapeutic role in mitigating environmental toxins affecting oocyte health.
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