AI Article Synopsis

  • Many women experience significant changes during menopause, including decreased bone mass and increased body fat, related to rising levels of the hormone FSH.
  • This study creates a mouse model (OVF) to examine the effects of FSH while controlling estrogen levels, using ovariectomized mice supplemented with estradiol.
  • The new OVF model is stable, cost-effective, and easy to use for research on how FSH affects conditions beyond the reproductive system.

Article Abstract

During the transition from a reproductive to a nonreproductive phase (menopause), many women experience significant physiological and pathological changes, including decreased bone mass, increased blood lipids, and increased visceral adiposity. Levels of follicle-stimulating hormone (FSH) rise during the menopausal transition. Many studies have shown that FSH in various extragonadal tissues and organs is associated with the pathogenesis of multiple diseases. Thus, building an animal model that can help study the independent effects of FSH in vivo is particularly important. In this study, C57BL/6 female mice were ovariectomized and supplemented with estradiol valerate (OVX + E2) to eliminate the effect of the hypothalamic-pituitary-gonadal axis. The OVX + E2 mice received solvent (N.S.) or different doses of recombinant FSH via intraperitoneal injection to create a mouse model (OVF) characterized by relatively stable estrogen and rising FSH levels. Thus, we successfully generated an experimental mouse model to mimic the early stage of menopause transition, characterized by elevated serum FSH levels. The OVF model has the advantages of being stable, low cost, and easy to operate, which is suitable for studies to explore the extragonadal actions of FSH. Here, we describe detailed protocols for the mouse OVF model.

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Source
http://dx.doi.org/10.3791/65665DOI Listing

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