Key result
Preeclamptic uterine placental beds had significantly higher angiotensin II peptide levels and renin and angiotensin-converting enzyme mRNA expression compared to normal pregnant subjects.
Observational (n=53)
The maternal uterine placental bed in preeclampsia shows increased angiotensin II and renin-angiotensin system component expression, suggesting a localized endocrine role in vasoconstricting fetal vessels.
Does not support practice changes in preeclampsia; leaves open placental RAS as a therapeutic target pending prospective studies.
Previously, we demonstrated activation of the renin-angiotensin system in the fetal placental chorionic villi, but it is unknown whether the immediately adjacent area of the maternal uterine placental bed is regulated similarly. This study measured angiotensin peptides, renin-angiotensin system component mRNAs, and receptor binding in the fundus from nonpregnant subjects (n = 19) and in the uterine placental bed from normal (n = 20) and preeclamptic (n = 14) subjects. In the uterine placental bed from normal pregnant women, angiotensin II peptide levels and angiotensinogen, angiotensin-converting enzyme, angiotensin receptor type 1 (AT(1)), AT(2), and Mas mRNA expression were lower as compared with the nonpregnant subjects. In preeclamptic uterine placental bed, angiotensin II peptide levels and renin and angiotensin-converting enzyme mRNA expression were significantly higher than normal pregnant subjects. The AT(2) receptor was the predominant receptor subtype in the nonpregnant fundus, whereas all angiotensin receptor binding was undetectable in normal and preeclamptic pregnant uterine placental bed compared with nonpregnant fundus. These findings suggest that the maternal uterine placental bed may play an endocrine role by producing angiotensin II, which acts in the adjacent placenta to vasoconstrict fetal chorionic villi vessels where we have shown previously that AT(1) receptors predominate. This would lead to decreased maternal-fetal oxygen exchange and fetal nutrition, a known characteristic of preeclampsia.
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Anton et al. (2009) conducted an observational in Preeclampsia (n=53). Preeclampsia vs. Normal pregnancy and nonpregnant state was evaluated on Angiotensin peptides, renin-angiotensin system component mRNAs, and receptor binding. Preeclamptic uterine placental beds had significantly higher angiotensin II peptide levels and renin and angiotensin-converting enzyme mRNA expression compared to normal pregnant subjects.
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