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1.
Endocrinology ; 163(9)2022 09 01.
Article in English | MEDLINE | ID: mdl-35776497

ABSTRACT

Polycystic ovarian syndrome (PCOS) is a complex health condition associated with metabolic disturbances and infertility. Recent data suggest that the prevalence of PCOS is increasing among women globally, although the etiology of these trends is undefined. Consequently, preclinical models that better reflect the biology of PCOS are urgently needed to facilitate research that can lead to the discovery of prevention strategies or improved management. The existing animal models have several limitations as they do not reflect all the PCOS features metabolically and/or phenotypically. Therefore, there is no clear consensus on the use of appropriate animal model and selection of the most appropriate PCOS-inducing agent. To that end, we have established a Swiss albino mouse model of PCOS based on 3 weeks of daily treatment with letrozole (50 µg/day; intraperitoneal) and dehydroepiandrosterone (DHEA, 6 mg/100 g body weight; subcutaneous) in 5-week-old female mice fed on normal or high-fat diet (HFD). Mice were regularly assessed for body weight, blood glucose, and estrous cycle. Three weeks after drug administration, mice were sacrificed and assessed for blood-based metabolic parameters as well as ovarian function. Our results indicate that DHEA combined with HFD produces changes mimicking those of clinical PCOS, including elevated serum testosterone and luteinizing hormone, dyslipidemia, poor ovarian microenvironment, and development of multiple ovarian cysts, recapitulating cardinal features of PCOS. In comparison, normal diet and/or letrozole produced fewer features of PCOS. The data from the experimental models presented here can improve our understanding of PCOS, a growing concern in women's health.


Subject(s)
Polycystic Ovary Syndrome , Animals , Body Weight , Dehydroepiandrosterone , Diet, High-Fat/adverse effects , Disease Models, Animal , Female , Humans , Letrozole , Mice , Polycystic Ovary Syndrome/metabolism , Tumor Microenvironment
2.
Reprod Fertil Dev ; 32(14): 1169-1179, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32998795

ABSTRACT

The present study was designed to investigate the effect of diet-induced obesity on endoplasmic reticulum (ER) stress in oocytes. Swiss albino mice (3 weeks old) were fed with a high-fat diet (HFD) for 8 weeks. Oocytes were assessed for lipid droplet accumulation, oxidative stress, ER stress and their developmental potential invitro. High lipid accumulation (P<0.01) and elevated intracellular levels of reactive oxygen species were observed in both germinal vesicle and MII oocytes of HFD-fed mice (P<0.05 and P<0.01 respectively compared with control). Further, expression of the ER stress markers X-box binding protein 1 (XBP1), glucose-regulated protein 78 (GRP78), activating transcription factor 4 (ATF4) and activating transcription factor 6 (ATF6) was significantly (P<0.001) higher in oocytes of the HFD than control group. Oocytes from HFD-fed mice exhibited poor fertilisation and blastocyst rates, a decrease in total cell number and high levels of DNA damage (P<0.01) compared with controls. In conclusion, diet-induced obesity resulted in elevated lipid levels and higher oxidative and ER stress in oocytes, which contributed to the compromised developmental potential of embryos.


Subject(s)
Embryonic Development/physiology , Endoplasmic Reticulum Stress/physiology , Lipid Metabolism/physiology , Oocytes/metabolism , Oxidative Stress/physiology , Activating Transcription Factor 4/metabolism , Activating Transcription Factor 6/metabolism , Animals , DNA Damage , Diet, High-Fat , Endoplasmic Reticulum Chaperone BiP , Female , Heat-Shock Proteins/metabolism , Mice , Obesity/metabolism , Reactive Oxygen Species/metabolism , X-Box Binding Protein 1/metabolism
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