Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum

Background Preeclampsia (PE) is characterized as de novo hypertension (HTN) with end-organ damage, especially in the brain. PE is hypothesized to be caused by placental ischemia. PE affects ~5–8% of USA pregnancies and increases the risk for HTN and cerebrovascular diseases (CVD) later in life. We h...

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Main Authors: Savanna Smith, Jonna Smith, Kylie Jones, Angie Castillo, Natalia Wiemann, Ahfiya Howard, Mark Cunningham
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Hypertension in Pregnancy
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Online Access:https://www.tandfonline.com/doi/10.1080/10641955.2025.2454597
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author Savanna Smith
Jonna Smith
Kylie Jones
Angie Castillo
Natalia Wiemann
Ahfiya Howard
Mark Cunningham
author_facet Savanna Smith
Jonna Smith
Kylie Jones
Angie Castillo
Natalia Wiemann
Ahfiya Howard
Mark Cunningham
author_sort Savanna Smith
collection DOAJ
description Background Preeclampsia (PE) is characterized as de novo hypertension (HTN) with end-organ damage, especially in the brain. PE is hypothesized to be caused by placental ischemia. PE affects ~5–8% of USA pregnancies and increases the risk for HTN and cerebrovascular diseases (CVD) later in life. We hypothesize that blood pressure (BP), cerebral oxidative stress, and cerebral inflammation will increase in postpartum (PP) placental ischemic dams.Methods Placental ischemia was induced in pregnant Sprague Dawley dams, utilizing reduced uterine perfusion pressure (RUPP) surgery. At 6 weeks PP (~3 human years), BP was measured via carotid catheterization, and cerebral oxidative stress and inflammation were assessed via ELISAs, biochemical assays, and Western blots.Results BP, cerebral pro-inflammatory cytokines (TNF-α and IL-6), and GFAP (a marker of astrocyte activity) were increased in PP RUPP dams. Cerebral hydrogen peroxide (H2O2) was also increased in PP RUPP dams, and had a strong correlation with PP RUPP BP, proinflammatory cytokines (TNF- α and IL-6), and GFAP astrocyte activation.Conclusion PP RUPP dams have increased BP, cerebral oxidative stress, and cerebral inflammation at 6 weeks postpartum. These changes in cerebral inflammation and oxidative stress may contribute to the pathology and development of HTN and CVDs in postpartum dams.
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spelling doaj-art-9dc668e7dc9e42469573e917e72d0b762025-01-31T04:44:23ZengTaylor & Francis GroupHypertension in Pregnancy1064-19551525-60652025-12-0144110.1080/10641955.2025.2454597Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartumSavanna Smith0Jonna Smith1Kylie Jones2Angie Castillo3Natalia Wiemann4Ahfiya Howard5Mark Cunningham6Department of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, USADepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, USADepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, USADepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, USATexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX, USASchool of Social Work, Texas A & M University-Commerce, Commerce, TX, USADepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, USABackground Preeclampsia (PE) is characterized as de novo hypertension (HTN) with end-organ damage, especially in the brain. PE is hypothesized to be caused by placental ischemia. PE affects ~5–8% of USA pregnancies and increases the risk for HTN and cerebrovascular diseases (CVD) later in life. We hypothesize that blood pressure (BP), cerebral oxidative stress, and cerebral inflammation will increase in postpartum (PP) placental ischemic dams.Methods Placental ischemia was induced in pregnant Sprague Dawley dams, utilizing reduced uterine perfusion pressure (RUPP) surgery. At 6 weeks PP (~3 human years), BP was measured via carotid catheterization, and cerebral oxidative stress and inflammation were assessed via ELISAs, biochemical assays, and Western blots.Results BP, cerebral pro-inflammatory cytokines (TNF-α and IL-6), and GFAP (a marker of astrocyte activity) were increased in PP RUPP dams. Cerebral hydrogen peroxide (H2O2) was also increased in PP RUPP dams, and had a strong correlation with PP RUPP BP, proinflammatory cytokines (TNF- α and IL-6), and GFAP astrocyte activation.Conclusion PP RUPP dams have increased BP, cerebral oxidative stress, and cerebral inflammation at 6 weeks postpartum. These changes in cerebral inflammation and oxidative stress may contribute to the pathology and development of HTN and CVDs in postpartum dams.https://www.tandfonline.com/doi/10.1080/10641955.2025.2454597Preeclampsiapostpartuminflammationoxidative stresshypertension
spellingShingle Savanna Smith
Jonna Smith
Kylie Jones
Angie Castillo
Natalia Wiemann
Ahfiya Howard
Mark Cunningham
Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum
Hypertension in Pregnancy
Preeclampsia
postpartum
inflammation
oxidative stress
hypertension
title Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum
title_full Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum
title_fullStr Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum
title_full_unstemmed Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum
title_short Placental ischemia during pregnancy induces hypertension, cerebral inflammation, and oxidative stress in dams postpartum
title_sort placental ischemia during pregnancy induces hypertension cerebral inflammation and oxidative stress in dams postpartum
topic Preeclampsia
postpartum
inflammation
oxidative stress
hypertension
url https://www.tandfonline.com/doi/10.1080/10641955.2025.2454597
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