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Melatonin prevents postovulatory oocyte aging in the mouse and extends the window for optimal fertilization in vitro

Melatonin prevents postovulatory oocyte aging in the mouse and extends the window for optimal fertilization in vitro
Melatonin prevents postovulatory oocyte aging in the mouse and extends the window for optimal fertilization in vitro
The quality of metaphase II oocytes deteriorates rapidly following ovulation as the result of an aging process associated with impaired fertilizing potential, disrupted developmental competence and an increased likelihood of embryonic resorption. As oxidative stress has been shown to accelerate the onset of apoptosis in oocytes and influence their capacity for fertilization, this study aimed to characterize the significance of such stress in the post-ovulatory aging of mouse oocytes in vitro. In the course of these studies, we investigated the ability of the potent antioxidant, melatonin, to arrest the aging process when used to supplement oocyte culture medium. This study demonstrated that oxidative stress may occur in oocytes after as little as 8 h in culture and coincides with the appearance of early apoptotic markers such as phosphatidylserine externalization, and is followed 16 h later by caspase activation (P < 0.05) and morphological evidence of oocyte senescence (P < 0.001). Importantly, supplementation of oocyte culture medium with 1 mM melatonin was able to significantly relieve the time-dependent appearance of oxidative stress in oocytes (P < 0.05) and, as a result, significantly delay the onset of apoptosis (P < 0.05). Furthermore, melatonin supplementation extended the optimal window for fertilization of oocytes aged for 8 h and 16 h in vitro (P < 0.05), and significantly improved the quality of the resulting embryos (P < 0.01). We conclude that melatonin may be a useful tool in a clinical setting to prevent the time-dependent deterioration of oocyte quality following prolonged culture in vitro.

Summary: Addition of the antioxidant melatonin to oocyte culture media delays the onset of post-ovulatory oocyte apoptosis; it not only extends the window for optimum fertilization but also improves the quality of resulting blastocysts.
oocyte aging, apoptosis, antioxidants, melatonin, oxidative stress
1-9
Lord, T.
afc32720-d852-4046-b7b4-9218894a88e6
Nixon, B.
a2d5a780-57a5-499a-81b2-5e05d4b69603
Jones, K.T.
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4
Aitken, R.J.
412d659b-ea02-490f-b758-f48f630219dd
Lord, T.
afc32720-d852-4046-b7b4-9218894a88e6
Nixon, B.
a2d5a780-57a5-499a-81b2-5e05d4b69603
Jones, K.T.
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4
Aitken, R.J.
412d659b-ea02-490f-b758-f48f630219dd

Lord, T., Nixon, B., Jones, K.T. and Aitken, R.J. (2013) Melatonin prevents postovulatory oocyte aging in the mouse and extends the window for optimal fertilization in vitro. Biology of Reproduction, 88 (3), 1-9, [67]. (doi:10.1095/biolreprod.112.106450). (PMID:23365415)

Record type: Article

Abstract

The quality of metaphase II oocytes deteriorates rapidly following ovulation as the result of an aging process associated with impaired fertilizing potential, disrupted developmental competence and an increased likelihood of embryonic resorption. As oxidative stress has been shown to accelerate the onset of apoptosis in oocytes and influence their capacity for fertilization, this study aimed to characterize the significance of such stress in the post-ovulatory aging of mouse oocytes in vitro. In the course of these studies, we investigated the ability of the potent antioxidant, melatonin, to arrest the aging process when used to supplement oocyte culture medium. This study demonstrated that oxidative stress may occur in oocytes after as little as 8 h in culture and coincides with the appearance of early apoptotic markers such as phosphatidylserine externalization, and is followed 16 h later by caspase activation (P < 0.05) and morphological evidence of oocyte senescence (P < 0.001). Importantly, supplementation of oocyte culture medium with 1 mM melatonin was able to significantly relieve the time-dependent appearance of oxidative stress in oocytes (P < 0.05) and, as a result, significantly delay the onset of apoptosis (P < 0.05). Furthermore, melatonin supplementation extended the optimal window for fertilization of oocytes aged for 8 h and 16 h in vitro (P < 0.05), and significantly improved the quality of the resulting embryos (P < 0.01). We conclude that melatonin may be a useful tool in a clinical setting to prevent the time-dependent deterioration of oocyte quality following prolonged culture in vitro.

Summary: Addition of the antioxidant melatonin to oocyte culture media delays the onset of post-ovulatory oocyte apoptosis; it not only extends the window for optimum fertilization but also improves the quality of resulting blastocysts.

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More information

e-pub ahead of print date: 30 January 2013
Published date: 2013
Keywords: oocyte aging, apoptosis, antioxidants, melatonin, oxidative stress
Organisations: Centre for Biological Sciences

Identifiers

Local EPrints ID: 349635
URI: http://eprints.soton.ac.uk/id/eprint/349635
PURE UUID: 26d3eb46-ff4d-4ba7-8847-60f87d3515db
ORCID for K.T. Jones: ORCID iD orcid.org/0000-0002-0294-0851

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Date deposited: 07 Mar 2013 16:31
Last modified: 14 Mar 2024 13:16

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Contributors

Author: T. Lord
Author: B. Nixon
Author: K.T. Jones ORCID iD
Author: R.J. Aitken

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