4.6 Article

Melatonin restores the declining maturation quality and early embryonic development of oocytes in aged mice

Journal

THERIOGENOLOGY
Volume 210, Issue -, Pages 110-118

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.theriogenology.2023.07.021

Keywords

Melatonin; Aged mice; Oocyte quality; Embryo development; Reactive oxygen species

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With the increase in women's age, the reproductive capability of female mammals decreases dramatically due to age-related oxidative stress, leading to a decline in the ovarian reserve and the quality and quantity of oocytes. Melatonin, an effective antioxidant and antiaging substance, has been found to protect oocytes from oxidative stress during ovulation. This study aimed to explore the potential mechanism of melatonin in improving oocytes maturation and early embryonic development. The results showed that melatonin supplementation significantly improved the maturation quality of oocytes, fertilization rate, and blastocyst formation rate by restoring mitochondrial function and increasing ATP and total GSH levels. This study provides a potential strategy to improve the quality of oocytes from aged women and the efficiency of assisted reproductive technologies.
With increase in women's age, the reproductive capability of female mammals decreases dramatically caused by age-related oxidative stress, coinciding with the decline in the ovarian reserve, and the quality and quantity of oocytes, which is the main determinant of female fertility. Melatonin, as an effective antioxidant and antiaging substance, is secreted by the pineal gland and been found in the follicular fluid as well, which has been turned out to enable to protect oocytes from oxidative stress during ovulation. However, the beneficial effects of melatonin on meiotic maturation in vitro and early embryo development of aged oocytes are still not fully understood. Thus, the aim of this study is to explore the potential mechanism of melatonin to improve the oo-cytes maturation and early embryonic development. The results suggested that oocyte quality decreased with age, whereas 10-6 M melatonin supplementation can significantly prompt the maturation quality of oocytes, the rate of fertilization and the formation rate of blastocyst. Mechanistic investigation indicated that melatonin supplementation not only restored the function of mitochondria by reducing reactive oxygen species (ROS) generation and early apoptosis, but also increased the level of ATP and total GSH through enhancing the mRNA expression levels of SIRT1, SIRT3, GPX4, SOD1 and SOD2. In conclusion, melatonin could alleviate the impairment of age-related oxidative stress to meiotic maturation and early embryonic development of oocytes. This study may provide a potential remediation strategy to improve the quality of oocytes from aged women and the efficiency of assisted reproductive technologies.

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