# Estradiol is not protective against angiotensin II‐induced hypertension in middle‐aged ovariectomized rats

**Authors:** A. P. O. Leite, I. Pires dos Santos, Y. Zha, S. A. Blessinger, H. Petillo, N. Jasti, H. C. Cheeran, R. Menon, A. B. Walker, J. M. Daniel, S. H. Lindsey

PMC · DOI: 10.14814/phy2.70646 · 2025-11-07

## TL;DR

Estradiol does not protect against high blood pressure and kidney damage in middle-aged rats with preexisting hypertension, suggesting hormone therapy may not help all menopausal women.

## Contribution

This study shows estradiol fails to protect against angiotensin II-induced hypertension in ovariectomized rats with preexisting hypertension.

## Key findings

- Estradiol exacerbated kidney damage and failed to reduce oxidative stress in hypertensive rats.
- Estradiol attenuated cardiac hypertrophy but worsened proteinuria and reduced glomerular filtration rate.
- Preexisting hypertension blunted the protective effects of estradiol on the vasculature and kidneys.

## Abstract

Menopause leads to loss of cardiovascular and renal protection, and while hormone therapy offers benefits, its efficacy may depend on health status at menopause onset. We hypothesized that preexisting hypertension blunts the renal, cardiac, and vascular effects of Estradiol (E2). Female Long‐Evans rats were ovariectomized (OVX) at 46 weeks to model menopause and received either E2 or vehicle, and some were infused with angiotensin II (ANG; 700 ng/kg/min) 4 weeks before OVX. Blood pressure (BP) was measured by tail cuff, renal function by urine collection, collagen deposition by histology, and mRNA expression in aorta and kidney by droplet digital PCR. ANG increased BP and proteinuria (p = 0.02), water intake (p < 0.001), urinary output, heart weight, and aortic NOX4 (p < 0.01), confirming hypertension and oxidative stress. E2 reduced body weight (p = 0.02), increased bone mineral content (p = 0.01), and prevented uterine atrophy (p < 0.001), confirming E2 treatment. While E2 attenuated cardiac hypertrophy (p = 0.004), it exacerbated proteinuria, decreased GFR (p < 0.05), and failed to reduce aortic NOX4. ANG did not affect tissue estrogen receptor expression, while E2 showed tissue‐specific regulation of GPER and ERα. In this hypertensive OVX model, E2 failed to protect renal and vascular damage, emphasizing the importance of cardiovascular health at menopause when considering hormone therapy.

Estradiol fails to protect in menopausal hypertension.

## Linked entities

- **Proteins:** NOX4 (NADPH oxidase 4), GPER1 (G protein-coupled estrogen receptor 1), ESR1 (estrogen receptor 1)
- **Chemicals:** estradiol (PubChem CID 450), angiotensin II (PubChem CID 65143)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Nox4 (NADPH oxidase 4) [NCBI Gene 85431], Agt (angiotensinogen) [NCBI Gene 24179] {aka ANRT, Ang, AngII, PAT}, Gper1 (G protein-coupled estrogen receptor 1) [NCBI Gene 171104] {aka GPR41, Gper, Gpr30}, Esr1 (estrogen receptor 1) [NCBI Gene 24890] {aka ER-alpha, Esr, RNESTROR}
- **Diseases:** hypertension (MESH:D006973), proteinuria (MESH:D011507), renal and vascular damage (MESH:D007674), uterine atrophy (MESH:D001284), cardiac hypertrophy (MESH:D006332)
- **Chemicals:** E2 (MESH:D004958)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12594632/full.md

---
Source: https://tomesphere.com/paper/PMC12594632