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Related Concept Videos

Ovarian Cycle01:27

Ovarian Cycle

The menstrual cycle includes a critical component known as the ovarian cycle, which undergoes two main phases each month—the follicular phase and the luteal phase. The follicular phase is variable and averaging around 14 days. Ovulation, triggered by a surge in luteinizing hormone (LH), marks the transition between the two phases. The second phase, the luteal phase, is relatively consistent, lasting approximately 14 days, and is marked by the activity of the corpus luteum. While a cycle length...
Oogenesis02:07

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...
Oogenesis01:22

Oogenesis

Oogenesis,  the process of developing egg cells (female gametes), occurs within the ovaries and is fundamental to female fertility. This sequence begins during fetal development when diploid oogonia in the developing ovaries undergo mitotic divisions to produce primary oocytes. By birth, these primary oocytes enter prophase I of meiosis but become arrested in this stage, remaining suspended until puberty.
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Hormonal Control of the Ovarian Cycle01:30

Hormonal Control of the Ovarian Cycle

The ovarian cycle is meticulously regulated by the hypothalamic-pituitary-gonadal axis. This cycle orchestrates the release of a mature oocyte, essential for reproduction.
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Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
Hormonal Regulation of the Menstrual Cycle01:22

Hormonal Regulation of the Menstrual Cycle

The ovarian cycle regulates endometrial changes throughout a single menstrual cycle via the coordinated action of gonadotrophin-releasing hormone (GnRH) and gonadotrophins.
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Establishment of an Embryo Implantation Model In Vitro
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Hormone-induced delayed ovulation affects early embryonic development.

Ann-Kathrin Bittner1, Bernhard Horsthemke, Elke Winterhager

  • 1Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Fertility and Sterility
|April 9, 2011
PubMed
Summary
This summary is machine-generated.

Delayed ovulation in mice, induced by cetrorelix, negatively impacted embryonic development. This resulted in more resorption sites and lower embryonic weight, suggesting potential fertility issues during assisted reproductive technology (ART).

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Area of Science:

  • Reproductive Biology
  • Developmental Biology
  • Assisted Reproductive Technology (ART)

Background:

  • Oocyte development can be delayed during human assisted reproductive technology (ART).
  • Understanding the impact of delayed ovulation on embryonic development is crucial for improving ART outcomes.

Purpose of the Study:

  • To investigate the effects of delayed ovulation on embryonic development in a mouse model.
  • To analyze how intrafollicular oocyte maturation delays influence fertility and offspring development.

Main Methods:

  • Experimental study using female C57Bl/6 mice.
  • Cetrorelix (GnRH-antagonist) was administered with follicle stimulation to delay ovulation.
  • Ovulation was induced with hCG; controls received stimulation without ovulation delay.
  • Ovarian assessments (follicles, corpora lutea) and embryonic development parameters (weight, resorption sites) were evaluated.

Main Results:

  • Cetrorelix effectively inhibited ovulation, evidenced by increased tertiary follicles and reduced follicle rupture/corpora lutea.
  • Delayed ovulation significantly increased the number of resorption sites.
  • A significant decrease in embryonic weight was observed in the delayed ovulation group.

Conclusions:

  • Preovulatory oocyte overripeness, induced by delayed ovulation, adversely affects fertility.
  • These findings suggest that oocyte aging during ART may compromise embryonic development and successful implantation.