Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/52406
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Type: Journal article
Title: Peroxisome proliferator-activated receptor-γ agonist rosiglitazone reverses the adverse effects of diet-induced obesity on oocyte quality
Other Titles: Peroxisome proliferator-activated receptor-gamma agonist rosiglitazone reverses the adverse effects of diet-induced obesity on oocyte quality
Author: Haynes, C.
Bennett, B.
Norman, R.
Robker, R.
Citation: Endocrinology, 2008; 149(5):2646-2656
Publisher: Endocrine Soc
Issue Date: 2008
ISSN: 0013-7227
0013-7227
Statement of
Responsibility: 
Cadence E. Minge, Brenton D. Bennett, Robert J. Norman and Rebecca L. Robker
Abstract: Obesity and its physiological consequences are increasingly prevalent among women of reproductive age and are associated with infertility. To investigate, female mice were fed a high-fat diet until the onset of insulin resistance, followed by assessments of ovarian gene expression, ovulation, fertilization, and oocyte developmental competence. We report defects to ovarian function associated with diet-induced obesity (DIO) that result in poor oocyte quality, subsequently reduced blastocyst survival rates, and abnormal embryonic cellular differentiation. To identify critical cellular mediators of ovarian responses to obesity induced insulin resistance, DIO females were treated for 4 d before mating with an insulin-sensitizing pharmaceutical: glucose and lipid-lowering AMP kinase activator, 5-aminoimidazole 4-carboxamide-riboside, 30 mg/kg.d; sodium salicylate, IkappaK inhibitor that reverses insulin resistance, 50 mg/kg.d; or peroxisome proliferator activated receptor-gamma agonist rosiglitazone, 10 mg/kg.d. 5-aminoimidazole 4-carboxamide-riboside or sodium salicylate treatment did not have significant effects on the reproductive parameters examined. However, embryonic development to the blastocyst stage was significantly improved when DIO mice were treated with rosiglitazone, effectively repairing development rates. Rosiglitazone also normalized DIO-associated abnormal blastomere allocation to the inner cell mass. Such improvements to oocyte quality were coupled with weight loss, improved glucose metabolism, and changes in ovarian mRNA expression of peroxisome proliferator activated receptor-regulated genes, Cd36, Scarb1, and Fabp4 cholesterol transporters. These studies demonstrate that peri-conception treatment with select insulin-sensitizing pharmaceuticals can directly influence ovarian functions and ultimately exert positive effects on oocyte developmental competence. Improved blastocyst quality in obese females treated with rosiglitazone before mating indicates that peroxisome proliferator activated receptor-gamma is a key target for metabolic regulation of ovarian function and oocyte quality.
Keywords: Ovary
Oocytes
Blastomeres
Cells, Cultured
Animals
Mice, Inbred C57BL
Mice
Obesity
Thiazolidinediones
PPAR gamma
Hypoglycemic Agents
Embryo Culture Techniques
Diet
Diet, Atherogenic
Cell Differentiation
Gene Expression Regulation
Embryonic Development
Ovulation
Cytoprotection
Female
Embryo, Mammalian
Rosiglitazone
Rights: Peroxisome proliferator-activated receptor-gamma agonist rosiglitazone reverses the adverse effects of diet-induced obesity on oocyte quality
DOI: 10.1210/en.2007-1570
Published version: http://dx.doi.org/10.1210/en.2007-1570
Appears in Collections:Aurora harvest
Obstetrics and Gynaecology publications

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