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Related Concept Videos

Fetal Circulation01:14

Fetal Circulation

Fetal circulation is a unique system that facilitates the exchange of gases, nutrients, and waste products between the developing fetus and the mother. This intricate process takes place through a special organ called the placenta.
Two umbilical arteries transport blood from the fetus to the placenta. At the placenta, the blood absorbs oxygen and nutrients while simultaneously eliminating waste products. This oxygen-enriched and nutrient-rich blood then returns to the fetus through one...
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The renin-aldosterone system is an endocrine system which guides the renal absorption of water and electrolytes, thus managing blood pressure and osmoregulation. Activation of the system begins in the kidneys with a small cluster of cells adjacent to the afferent and efferent blood vessels of the renal corpuscle. As the nephrons are filtering blood, juxtaglomerular cells monitor blood pressure. If they detect a decrease in pressure, they release the hormone renin into the bloodstream.
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Gonadal and Placental Hormones

The gonads, namely the testes in males and the ovaries in females, are pivotal in producing gonadal hormones that orchestrate the intricate processes of sexual development and reproduction.
In males, testosterone is the primary gonadal androgen. It plays a central role in the maturation of male reproductive organs — the penis and testes. Additionally, testosterone is instrumental in the development of secondary sexual characteristics — a deep voice as well as facial and pubic hair growth — and...
Development of Blood Vessels01:07

Development of Blood Vessels

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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...
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Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
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Disruption of the Mouse Blood-Brain Barrier by Small Extracellular Vesicles from Hypoxic Human Placentas
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Published on: January 26, 2024

The placenta in preeclampsia.

James M Roberts1, C Escudero

  • 1Magee Women Research Institute, Department of Obstetrics and Gynecology, Epidemiology and Clinical and Translational Research, University of Pittsburgh, USA.

Pregnancy Hypertension
|June 30, 2012
PubMed
Summary
This summary is machine-generated.

Preeclampsia pathophysiology is rooted in placental changes. This study compares placental abnormalities in preeclampsia and fetal growth restriction (FGR), revealing inconsistent differences and highlighting areas needing further research for better understanding.

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Area of Science:

  • Obstetrics and Gynecology
  • Maternal-Fetal Medicine
  • Pathology

Background:

  • The placenta is the root cause of preeclampsia, with symptoms abating upon its delivery.
  • Preeclampsia can occur without a fetus, emphasizing the placenta's central role.
  • Studying placental pathophysiology is crucial for understanding preeclampsia.

Purpose of the Study:

  • To examine placental pathological and pathophysiological changes in preeclampsia and fetal growth restriction (FGR).
  • To compare placental findings in early-onset versus late-onset preeclampsia.
  • To identify key differences and similarities between preeclampsia and FGR placentation.

Main Methods:

  • Comparative analysis of placental pathology in preeclampsia and FGR.
  • Examination of pathophysiological changes associated with both conditions.
  • Review of findings related to early and late-onset preeclampsia.

Main Results:

  • Placental abnormalities in preeclampsia align with predicted reduced perfusion and oxidative stress.
  • Differences between preeclampsia and FGR placental findings are inconsistent.
  • Significant differences observed in less-studied placental areas; early vs. late preeclampsia differences require further clarification.

Conclusions:

  • Placental study offers insights into preeclampsia pathophysiology, though direct comparisons with FGR show inconsistencies.
  • Further research is needed to clarify qualitative vs. quantitative differences in early-onset vs. late-onset preeclampsia.
  • Recommendations are provided to guide future studies in resolving discrepancies in placental findings.