# Fructose and salt induce sex- and ovary dependent cardiac hypertrophy in Dahl salt-sensitive rats

**Authors:** M. A. Akhtar, S. Ludvigsen, C. Mancusi, G. de Simone, A. D. Hafstad, E. Gerdts, K. Ytrehus

PMC · DOI: 10.3389/fcvm.2026.1753554 · Frontiers in Cardiovascular Medicine · 2026-03-18

## TL;DR

This study shows that fructose and salt cause heart changes in male and ovariectomized female rats, but not in intact females, highlighting the role of sex and hormones in heart disease.

## Contribution

The study reveals sex- and ovary-dependent differences in cardiac hypertrophy caused by high fructose and salt diets in hypertensive-prone rats.

## Key findings

- High-salt diet significantly increased blood pressure in all groups, with the highest in the high-salt group.
- Cardiac remodeling occurred in males and ovariectomized females but not in intact females on a high-salt diet.
- Gene expression changes in the heart included increased natriuretic peptides, fibrosis, and inflammation markers.

## Abstract

The consumption of sugar and salt plays a pivotal role in the development of metabolic disorders, hypertension, and subsequent cardiovascular morbidity. This study investigates the influence of sex and gonadal status on early signs of cardiac remodeling in hypertensive-prone Dahl salt-sensitive (DSS) rats by comparing male, female, and ovariectomized (OVX) female rats. DSS rats were provided with 10% fructose in their drinking water and subjected to either a high-salt diet (6% NaCl) or a standard-salt diet (0.3% NaCl) for 8 weeks. Mean arterial pressure, initially 115 ± 2 mmHg at baseline across all groups, increased to 127 ± 5 mmHg with the standard-salt diet and to 156 ± 7 mmHg with the high-salt diet (p < 0.001). High-salt intake was associated with significant concentric cardiac remodeling in OVX females and males but not in intact females. In parallel with these cardiac changes, gene expression analysis of left ventricular apex samples revealed increased mRNA levels of natriuretic peptides and genes associated with fibrosis and inflammation. These findings highlight a complex interplay between diet, sex hormones, and the pathophysiology of hypertensive cardiac disease. Further, this study underscores the importance of including both sexes and to consider gonadal status in hypertensive cardiac remodeling.

## Linked entities

- **Chemicals:** fructose (PubChem CID 5984), NaCl (PubChem CID 5234)

## Full-text entities

- **Diseases:** fibrosis (MESH:D005355), metabolic disorders (MESH:D008659), inflammation (MESH:D007249), cardiac remodeling (MESH:D020257), hypertension (MESH:D006973), cardiac hypertrophy (MESH:D006332), cardiac (MESH:D006331)
- **Chemicals:** Fructose (MESH:D005632), salt (MESH:D012492), NaCl (MESH:D012965), natriuretic peptides (MESH:D045265), sugar (MESH:D000073893)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13039016/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC13039016/full.md

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Source: https://tomesphere.com/paper/PMC13039016