Body fat affects mouse reproduction, ovarian hormone release, and response to follicular stimulating hormone

Reprod Biol. 2018 Mar;18(1):5-11. doi: 10.1016/j.repbio.2017.12.002. Epub 2017 Dec 8.

Abstract

We investigated the effects of body fat content on mouse fecundity, ovarian hormone release, and their response to follicle stimulation hormone (FSH). 4 types of females were produced: lean (group 1), normal (group 2), slightly fat (group 3), and significantly fat (group 4). The body weights, fat content, fertility rate, embryo number produced, retarded and degenerated embryo percentage, the release of progesterone (P4), testosterone (T), and insulin-like growth factor I (IGF-I) by isolated ovaries cultured with and without FSH (1.0IU/mL medium) were evaluated. A gradual increase in body weight and fat contents from groups 1 to 4 was observed. Group 2 had higher fertility rate than those from the other groups. Groups 2 and 3 had fewer retarded and degenerated embryos that those from groups 1 and 4. Embryo production rate was not different among the groups. P4 and T secretion was higher from group 4 than in those from groups 1-3; secretion of IGF-I of group 3 was less than that of groups 1, 2, and 4. FSH promoted ovarian T output in all groups and stimulated ovarian P4 release in groups 1, 3, and 4, but not in group 2. FSH did not affect IGF-I release in any group. Therefore, both malnutrition and overfeeding can affect body weight and fat content in female mice, reducing embryo quality or developmental capacity, but not fertility and embryo production. Excess weight or fat can have stimulatory effects on ovarian P4 and T, but inhibitory effects on ovarian IGF-I release. Both leanness and excess weight or fat can induce the stimulatory action of FSH on ovarian P4.

Keywords: FSH; Fat; IGF-I; Ovary; Progesterone; Testosterone.

MeSH terms

  • Adiposity*
  • Animals
  • Drug Resistance
  • Embryonic Development
  • Female
  • Fertility Agents, Female / pharmacology*
  • Follicle Stimulating Hormone / pharmacology*
  • Infertility, Female / etiology
  • Infertility, Female / therapy
  • Insulin-Like Growth Factor I / metabolism
  • Litter Size
  • Maternal Nutritional Physiological Phenomena*
  • Mice, Inbred ICR
  • Obesity / metabolism
  • Obesity / physiopathology*
  • Organ Culture Techniques
  • Ovary / drug effects*
  • Ovary / metabolism
  • Overweight / metabolism
  • Overweight / physiopathology
  • Pregnancy
  • Progesterone / metabolism
  • Reproducibility of Results
  • Testosterone / metabolism
  • Thinness / metabolism
  • Thinness / physiopathology*
  • Weight Gain

Substances

  • Fertility Agents, Female
  • insulin-like growth factor-1, mouse
  • Testosterone
  • Progesterone
  • Insulin-Like Growth Factor I
  • Follicle Stimulating Hormone