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      Impact of gonadotropin administration on folliculogenesis in prepubertal ob/ob mice.

      Molecular and Cellular Endocrinology

      Apoptosis, drug effects, physiology, Body Weight, Cell Differentiation, Chorionic Gonadotropin, pharmacology, Estradiol, blood, Female, Follicular Atresia, Gonadotropins, Equine, Granulosa Cells, cytology, Leptin, deficiency, Mice, Mice, Inbred C57BL, Mice, Obese, Organ Size, Ovarian Follicle, Ovulation, Progesterone, Sexual Maturation, Animals

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          Abstract

          Female leptin deficient (ob/ob) mice exhibit abnormal ovarian folliculogenesis resulting in an impaired ability to reproduce. This effect may be related to the hypogonadotropic state of these animals, or leptin may directly modulate ovarian follicle development. In the present study we assessed whether exogenous gonadotropin administration would normalize folliculogenesis and induce ovulation in immature ob/ob animals. Eight 26-day-old ob/ob and eight control mice were injected sc with pregnant mare serum gonadotropin followed 48 h later with a sc injection of human chorionic gonadotropin. Animals were killed 24 h later. Gonadotropin (GTH) administration increased both ovarian and uterine weights in control mice, but this effect was attenuated in leptin deficient animals. The number of preantral follicles was greater in ob/ob mice than controls, but in GTH-treated animals the number of antral follicles was subnormal in the ovaries of leptin deficient animals. Ob/ob animals also failed to ovulate in response to GTH, and the protective actions of GTH against granulosa cell apoptosis and follicular atresia were attenuated in these animals. Interestingly, however, serum levels of estradiol and progesterone were higher in ob/ob mice than controls, regardless of whether or not the animals received GTH treatment. We conclude that the ovarian responsiveness to GTH is subnormal in leptin deficient animals suggesting that leptin may modulate the process of folliculogenesis by directly altering the sensitivity of the ovary to GTH.

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          Journal
          16337737
          10.1016/j.mce.2005.11.003

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