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Determination of the Transport Rate of Xenobiotics and Nanomaterials Across the Placenta using the ex vivo Human Placental Perfusion Model
Published on: June 18, 2013
Assessment of Placental Transport Function in Studies of Disease Programming
1Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK. ans48@cam.ac.uk.
Insights
Environmental factors during pregnancy impact fetal development and offspring health. Measuring placental nutrient transfer in vivo in mice helps understand fetal growth regulation and in utero disease programming.
Area of Science:
- Reproductive biology
- Developmental biology
- Maternal-fetal medicine
Background:
- Pregnancy environment influences fetal growth and long-term health.
- The placenta is crucial for nutrient transfer and fetal development.
- Understanding maternofetal transfer is key to fetal growth regulation.
Purpose of the Study:
- To describe a method for quantifying in vivo placental transfer function in mice.
- To provide a tool for studying in utero disease programming.
Main Methods:
- Utilizing non-metabolizable radio-analogues of glucose and amino acids.
- Measuring unidirectional maternofetal transfer in vivo.
- Applying the technique in a mouse model.
Main Results:
- The described method allows for quantification of placental transfer function.
- This technique is applicable to mouse models used in developmental programming studies.
Conclusions:
- In vivo measurement of placental transfer is vital for understanding fetal growth.
- The described mouse model method aids research into pregnancy-related health outcomes.
Abstract:
Environmental conditions during pregnancy affect fetal growth and development and program the offspring for poor future health. These effects may be mediated by the placenta, which develops to transfer nutrients from the mother to the fetus for growth. The ability to measure the unidirectional maternofetal transfer of non-metabolizable radio-analogues of glucose and amino acid by the placenta in vivo has thus been invaluable to our understanding of the regulation of fetal growth, particularly in small animal models. Herein, I describe the method by which in vivo placental transfer function can be quantified in the mouse, an animal model widely used in studies of in utero disease programming.
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