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

Developmental changes in the rat atriopeptin hormonal system.

Y F Wei, C P Rodi, M L Day

    The Journal of Clinical Investigation
    |May 1, 1987
    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

    Interleukin 13 (IL-13)-regulated expression of the chondroprotective metalloproteinase ADAM15 is reduced in aging cartilage.

    Osteoarthritis and cartilage open·2020
    Same author

    Role of progesterone concentrations during early follicular development in beef cattle: I. Characteristics of LH secretion and oocyte quality.

    Animal reproduction science·2018
    Same author

    Role of progesterone concentrations during early follicular development in beef cattle: II. Ovulatory follicle growth and pregnancy rates.

    Animal reproduction science·2018
    Same author

    Impact of a timed-release FSH treatment from 2 to 6 months of age in bulls II: Endocrinology, puberty attainment, and mature sperm production in Holstein bulls.

    Theriogenology·2017
    Same author

    Impact of a timed-release FSH treatment from 2 to 6 months of age in bulls I: Endocrine and testicular development of beef bulls.

    Theriogenology·2017
    Same author

    Fibulin-3 promotes muscle-invasive bladder cancer.

    Oncogene·2017
    Same journal

    Extracellular matrix reprogramming by the YAP/TAZ- TGF-ß2 axis drives immune exclusion in cholangiocarcinoma models.

    The Journal of clinical investigation·2026
    Same journal

    Tumor cell-derived extracellular vesicles foster the immunosuppressive landscape of pancreatic cancer.

    The Journal of clinical investigation·2026
    Same journal

    Julie Zikherman receives the ASCI/Marian W. Ropes, MD, Award.

    The Journal of clinical investigation·2026
    Same journal

    Targeted degradation of MDM2 overcomes feedback regulation of p53 signaling in Merkel cell carcinoma models.

    The Journal of clinical investigation·2026
    Same journal

    SGLT2 inhibitors enhance ketogenesis by acting as allosteric activators of the mitochondrial enzyme HMGCS2.

    The Journal of clinical investigation·2026
    Same journal

    MDM2 degraders for Merkel cell carcinoma: round peg in a round hole.

    The Journal of clinical investigation·2026
    See all related articles

    Fetal atriopeptin (AP) hormonal system is functional, with high fetal plasma levels potentially from maternal transfer and influenced by renal capacity. The fetus responds to stimuli, releasing AP, indicating a mature-like response to intracardiac pressure.

    Area of Science:

    • Cardiovascular Physiology
    • Endocrinology
    • Neonatal Research

    Background:

    • Atriopeptin (AP) plays a crucial role in cardiovascular homeostasis.
    • Understanding AP's role during fetal development is essential for neonatal health.
    • Limited data exists on fetal AP synthesis, storage, and release mechanisms.

    Purpose of the Study:

    • To investigate fetal atriopeptin (AP) synthesis, storage, and release.
    • To compare fetal and maternal AP levels and their regulation.
    • To determine the functional capacity of the fetal AP system.

    Main Methods:

    • Measurement of plasma atriopeptin immunoreactivity (APir) and NH2-terminal fragment immunoreactivity (NTFir) in fetuses and mothers.
    • Quantification of AP content in fetal and adult cardiac atria and ventricles.

    Related Experiment Videos

  • Analysis of AP messenger RNA (mRNA) levels in fetal and postnatal cardiac tissues.
  • Infusion studies with exogenous atriopeptin and administration of vasopressin and indomethacin.
  • Main Results:

    • Fetal plasma APir and NTFir levels were significantly higher than maternal levels.
    • Ventricular AP content was high in fetuses and decreased postnatally, while atrial content increased.
    • Fetal cardiac AP mRNA levels were high in ventricles and low in atria, with a postnatal shift.
    • Exogenous atriopeptin infusion to mothers caused parallel increases in fetal and maternal levels.
    • Fetal plasma AP levels reflected reduced renal metabolic capacity and responded to vasopressin and indomethacin stimuli.

    Conclusions:

    • The atriopeptin hormonal system is functional in the fetus.
    • Fetal AP levels are influenced by maternal transfer and renal function.
    • The fetal cardiovascular system demonstrates a mature-like response to stimuli increasing intracardiac pressure.