# Exposure to Fluoride During Pregnancy and Lactation Induces Metabolic Imbalance in Pancreas: A Toxicological Insight Using the Rat Model

**Authors:** Marta Skórka-Majewicz, Wojciech Żwierełło, Arleta Drozd, Irena Baranowska-Bosiacka, Donata Simińska, Agata Wszołek, Izabela Gutowska

PMC · DOI: 10.3390/ijms26199817 · 2025-10-09

## TL;DR

Chronic fluoride exposure during pregnancy and lactation in rats leads to pancreatic inflammation and disrupted hormone levels, potentially increasing diabetes risk.

## Contribution

This study reveals new insights into how fluoride exposure affects pancreatic endocrine function and inflammation in offspring rats.

## Key findings

- Fluoride exposure caused decreased serum insulin and somatostatin levels in rats.
- Pancreatic tissues showed elevated pro-inflammatory eicosanoids like prostaglandin E2 and leukotrienes.
- Chronic fluoride exposure disrupted pancreatic endocrine homeostasis and induced inflammation.

## Abstract

Fluoride is a widespread environmental toxin that disrupts metabolic and endocrine functions, but its impact on pancreatic inflammation and hormone secretion remains unclear. This study examined how chronic fluoride exposure affects pancreatic inflammation and secretory function in rats. Pregnant Wistar rats received sodium fluoride (NaF) at 50 mg/L in drinking water during gestation and lactation. Male offspring continued exposure until 3 months old. Controls received fluoride-free water. Pancreatic tissue and serum were collected. Fluoride levels were measured potentiometrically. Eicosanoids were quantified by SPE and HPLC. Serum insulin, glucagon, and somatostatin were measured by ELISA. Histological and biochemical markers of inflammation and oxidative stress were assessed. Fluoride exposure did not lead to significant accumulation in the pancreas or serum. However, fluoride-exposed rats exhibited a significant decrease in serum insulin and somatostatin concentrations, while glucagon levels remained unchanged. Additionally, the pancreas of fluoride-treated animals showed markedly elevated levels of pro-inflammatory eicosanoids, including prostaglandin E2, leukotrienes A4 and B4, and HETE/HODE derivatives, indicating activation of cyclooxygenase and lipoxygenase pathways. Sustained low-dose fluoride exposure induced pancreatic inflammation and disrupted endocrine homeostasis in rats. These findings suggest that chronic fluoride intake may impair insulin secretion and promote pre-diabetic alterations, warranting further research.

## Linked entities

- **Chemicals:** fluoride (PubChem CID 28179), sodium fluoride (PubChem CID 5235), prostaglandin E2 (PubChem CID 5280360)

## Full-text entities

- **Genes:** Sst (somatostatin) [NCBI Gene 24797] {aka SRIF, SS-14, SS-28, Smst}, Gcg (glucagon) [NCBI Gene 24952] {aka GLP-1, Glp1, Glp2}
- **Diseases:** inflammation (MESH:D007249), diabetic (MESH:D003920)
- **Chemicals:** HETE (MESH:D006893), prostaglandin E2 (MESH:D015232), water (MESH:D014867), Eicosanoids (MESH:D015777), NaF (MESH:D012969), Fluoride (MESH:D005459), HODE (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12525159/full.md

---
Source: https://tomesphere.com/paper/PMC12525159