Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/62284
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Type: Journal article
Title: Beta-oxidation is essential for mouse oocyte developmental competence and early embryo development
Author: Dunning, K.
Cashman, K.
Russell, D.
Thompson, J.
Norman, R.
Robker, R.
Citation: Biology of Reproduction, 2010; 83(6):909-918
Publisher: Soc Study Reproduction
Issue Date: 2010
ISSN: 0006-3363
1529-7268
Statement of
Responsibility: 
Kylie R. Dunning, Kara Cashman, Darryl L. Russell, Jeremy G. Thompson, Robert J. Norman, and Rebecca L. Robker
Abstract: Oocyte and embryo metabolism are closely linked with their subsequent developmental capacity. Lipids are a potent source of cellular energy, yet little is known about lipid metabolism during oocyte maturation and early embryo development. Generation of ATP from lipids occurs within mitochondria via beta-oxidation of fatty acids, with the rate-limiting step catalyzed by carnitine palmitoyl transferase I (CPT1B), a process also requiring carnitine. We sought to investigate the regulation and role of beta-oxidation during oocyte maturation and preimplantation development. Expression of Cpt1b mRNA, assessed by real-time RT-PCR in murine cumulus-oocyte complexes (COCs), increased following hormonal induction of oocyte maturation and ovulation in vivo with human chorionic gonadotropin (5 IU) and in embryos reaching the blastocyst stage. Beta-oxidation, measured by the production of 3H2O from [3H]palmitic acid, was significantly increased over that in immature COCs following induction of maturation in vitro with epidermal growth factor (3 ng/ml) and follicle-stimulating hormone (50 mIU/ml). The importance of lipid metabolism for oocyte developmental competence and early embryo development was demonstrated by assessing the rate of embryo development following inhibition or upregulation of beta-oxidation with etomoxir (an inhibitor of CPT1B) or l-carnitine, respectively. Inhibition of beta-oxidation during oocyte maturation or zygote cleavage impaired subsequent blastocyst development. In contrast, l-carnitine supplementation during oocyte maturation significantly increased beta-oxidation, improved developmental competence, and in the absence of a carbohydrate energy supply, significantly increased 2-cell cleavage. Thus, carnitine is an important cofactor for developing oocytes, and fatty acids are an important energy source for oocyte and embryo development.
Keywords: beta-oxidation; CPT1B; embryo development; fatty acid oxidation; oocyte maturation
Rights: © 2010 by the Society for the Study of Reproduction, Inc.
RMID: 0020101527
DOI: 10.1095/biolreprod.110.084145
Appears in Collections:Obstetrics and Gynaecology publications

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