Details

Autor(en) / Beteiligte

• Wu, Linda Lin-Yan
• Dunning, Kylie R
• Yang, Xing
• Russell, Darryl L
• Lane, Michelle
• Norman, Robert J
• Robker, Rebecca L

Titel

High-Fat Diet Causes Lipotoxicity Responses in Cumulus–Oocyte Complexes and Decreased Fertilization Rates

Ist Teil von

• Endocrinology (Philadelphia), 2010-11, Vol.151 (11), p.5438-5445

Ort / Verlag

Chevy Chase, MD: Endocrine Society

Erscheinungsjahr

2010

Quelle

Oxford Journals 2020 Medicine

Beschreibungen/Notizen

• In obesity, accumulation of lipid in nonadipose tissues, or lipotoxicity, is associated with endoplasmic reticulum (ER) stress, mitochondrial dysfunction, and ultimately apoptosis. We have previously shown that obese women have increased triglycerides in follicular fluid; thus, the present study examined whether high-fat diet–induced obesity causes lipotoxicity in granulosa cells and the cumulus–oocyte complex (COC). Oocytes of mice fed a high-fat diet had dramatically increased lipid content and reduced mitochondrial membrane potential compared to those of mice fed a control diet. COCs from mice fed a high-fat diet had increased expression of ER stress marker genes ATF4 and GRP78. Apoptosis was increased in granulosa and cumulus cells of mice fed a high-fat diet. Mice fed a high-fat diet also exhibited increased anovulation and decreased in vivo fertilization rates. Thus, lipid accumulation, ER stress, mitochondrial dysfunction, and apoptosis are markedly increased in ovarian cells of mice fed a high-fat diet. ER stress markers were also analyzed in granulosa cells and follicular fluid from women with varying body mass indices (BMI). ATF4 was increased in granulosa cells and [Ca2+] in follicular fluid from obese women compared to nonobese women. These results indicate that lipotoxicity may be occurring in ovarian cells of obese women and may contribute to the reduced pregnancy rates observed in response to obesity. The cumulus-oocyte complexes of mice fed a high fat diet exhibit distinct signs of lipotoxicity, namely lipid accumulation, endoplasmic reticulum stress, and increased apoptosis; similar responses may also be occurring in the ovarian cells of obese women.