Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Nitric oxide delays oocyte aging.

Anuradha P Goud1, Pravin T Goud, Michael P Diamond

  • 1Department of Obstetrics and Gynecology, The C.S. Mott Center for Human Growth and Development, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.

Biochemistry
|August 24, 2005
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Novel anti-Mullerian hormone receptor 2 binding peptide prevents chemotherapy-related ovarian follicle loss in a mouse model.

Journal of assisted reproduction and genetics·2026
Same author

Mechanisms of reproductive toxicity and endocrine disruption of bisphenols and per- and polyfluoroalkyl substances (PFAS): Implications for women's reproductive health.

Reproductive toxicology (Elmsford, N.Y.)·2026
Same author

Myeloperoxidase in the pathogenesis of sickle cell disease.

Archives of biochemistry and biophysics·2026
Same author

An updated look into reactive oxygen species and cyclophosphamide-induced ovarian damage.

Journal of ovarian research·2025
Same author

Vitamin D binding protein and reproductive outcomes.

Fertility and sterility·2025
Same author

The interplay between the myeloperoxidase-hypochlorous acid system, heme oxygenase, and free iron in inflammatory diseases.

Journal of inorganic biochemistry·2025
Same journal

Bilirubin Reductase from <i>Mediterraneibacter gnavus</i>: Positional Reduction Preferences and Transient-State Analysis.

Biochemistry·2026
Same journal

Aromatic Cage-Directed Azide-Methyllysine Photochemistry for Profiling Nonhistone Interacting Partners of the MeCP2 Methyl-CpG-Binding Domain.

Biochemistry·2026
Same journal

Differential Hydroxypyruvate Processing by <i>E. coli</i> and <i>P. aeruginosa</i> DXP Synthases Reveals Preferential Xylulose 5-Phosphate Formation by the <i>P. aeruginosa</i> Enzyme.

Biochemistry·2026
Same journal

Structural and Functional Characterization of Heterologous Nitrogenase Complexes.

Biochemistry·2026
Same journal

Discovery of Bacterial Unspecific Peroxygenases.

Biochemistry·2026
Same journal

Lactate Biology: Subcellular Routing and Chemical Form Define Function.

Biochemistry·2026
See all related articles

Nitric oxide (NO) delays oocyte aging and enhances spindle integrity in both young and old mouse oocytes. This study reveals NO

Area of Science:

  • Reproductive Biology
  • Cellular Signaling
  • Molecular Endocrinology

Background:

  • Nitric oxide (NO) is a vital signaling molecule in reproduction.
  • The specific impact of NO on oocyte aging remains largely unknown.
  • Understanding NO's role is crucial for reproductive health and fertility research.

Purpose of the Study:

  • To investigate the effects of nitric oxide (NO) on oocyte aging.
  • To determine NO's influence on key aging-related phenomena in oocytes.
  • To assess NO's impact on spindle and chromatin integrity during oocyte aging.

Main Methods:

  • Young and old mouse oocytes were exposed to varying concentrations of the NO donor, S-nitroso acetyl penicillamine (SNAP).
  • Ooplasmic microtubule dynamics (OMD), cortical granule (CG) exocytosis, zona pellucida (ZP) hardening, and spindle/chromatin integrity were analyzed.

Related Experiment Videos

  • Fluorescence immunocytochemistry and confocal microscopy were employed to evaluate aging markers.
  • Main Results:

    • NO exposure significantly reduced OMD and ZP dissolution time in both young and old oocytes.
    • Spontaneous CG loss decreased in old oocytes exposed to NO.
    • NO exposure reduced spindle abnormalities and demonstrated a dose-response relationship with aging markers.

    Conclusions:

    • Nitric oxide (NO) exposure delays oocyte aging.
    • NO improves the integrity of the microtubular spindle apparatus in oocytes.
    • These findings highlight NO's protective role in oocyte aging and quality.