Related Experiment Video
Updated: Jun 17, 2026

Using a Murine Model of Psychosocial Stress in Pregnancy as a Translationally Relevant Paradigm for Psychiatric Disorders in Mothers and Infants
Published on: June 13, 2021
Effect of prenatal dexamethasone on postnatal serum and urinary angiotensin II levels
Amit Dagan1, Jyothsna Gattineni, Sabeen Habib
1Department of Pediatrics, University of Texas Southwestern Medical Center at Dallas, TX, USA.
Insights
Prenatal dexamethasone exposure in rats leads to elevated urine angiotensin II levels, suggesting this peptide plays a role in developing hypertension. This finding offers insight into the mechanisms of prenatal programming of blood pressure.
Area of Science:
- Endocrinology
- Nephrology
- Developmental Biology
Background:
- Prenatal programming can lead to hypertension in offspring.
- The exact mechanisms behind this phenomenon remain unclear.
- Animal models are crucial for investigating these developmental origins of disease.
Purpose of the Study:
- To investigate the role of angiotensin II in hypertension development.
- To determine if angiotensin II contributes to the generation or maintenance of high blood pressure.
- To explore the effects of prenatal dexamethasone exposure on angiotensin II levels.
Main Methods:
- Male rats were exposed to dexamethasone in utero during critical gestational periods.
- Systemic and urinary levels of angiotensin II were measured at 4 and 8 weeks of age.
- Renal angiotensin II levels and urine angiotensin II/Creatinine ratios were analyzed.
Main Results:
- Offspring exposed to prenatal dexamethasone showed normal plasma renin and angiotensin II levels.
- Renal angiotensin II levels were similar between exposed and control groups.
- Significantly higher urine angiotensin II/Creatinine ratios were observed in the dexamethasone-exposed group.
Conclusions:
- Elevated urinary angiotensin II suggests a role for luminal angiotensin II in hypertension.
- This finding implicates angiotensin II in the generation and maintenance of hypertension.
- Luminal angiotensin II may be a key factor in prenatal programming of hypertension.
Background:
Prenatal programming of hypertension has been described in humans and in animal models that receive a prenatal insult, but the mechanism for the increase in blood pressure remains elusive.
Methods:
In male rats whose mothers received dexamethasone between days 15 and 18 of gestation systemic and urinary levels of angiotensin II were measured to determine whether angiotensin II was a potential factor for the generation (4 weeks of age) or maintenance (8 weeks of age) of hypertension.
Results:
A group 4- and 8-week-old male rats that were the product of a pregnancy where the mother received prenatal dexamethasone between days 15 and 18 of gestation had comparable plasma renin and angiotensin II levels to the offspring of vehicle-treated controls. Renal angiotensin II levels were not different at 4 and 8 weeks of age between the controls and the prenatal dexamethasone group. Urine angiotensin II/Creatinine levels, a reflection of filtered and renally generated and secreted angiotensin II, were higher at both 4 and 8 weeks of age in male rats that received prenatal dexamethasone compared to controls.
Conclusions:
The high-urine angiotensin II levels in prehypertensive and hypertensive rats that were the product of mothers that received dexamethasone compared to vehicle suggest that luminal angiotensin II may play a role in the generation and maintenance of hypertension in this model of prenatal programming.
Related Concept Videos
Hormonal Regulation
Teratogenicity
Antihypertensive Drugs: Direct Renin Inhibitors
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Hormonal Regulation of Blood Pressure
Epinephrine and Norepinephrine
The adrenal medulla releases epinephrine and norepinephrine, catecholamines that enhance and extend the sympathetic or "fight or flight" physiological response. These hormones escalate heart rate and the force of contraction while...
Hypertension II: Pathophysiology