# Acute toxic effects of Bothrops atrox venom on calcium homeostasis and bone tissue in mice

**Authors:** Hatem Kallel, Latifa Hamdaoui, Malek Elerou, Marwa Lakhrem, Stephanie Houcke, Majed Kammoun, Dabor Resiere, Tarek Rebai, Jean Marc Pujo, Ibtissem Ben Amara

PMC · DOI: 10.1016/j.toxcx.2025.100237 · Toxicon: X · 2025-12-08

## TL;DR

This study shows that Bothrops atrox venom harms bone health in mice by disrupting calcium balance, increasing oxidative stress, and damaging bone structure.

## Contribution

The study reveals new insights into how B. atrox venom affects bone metabolism and structural integrity in mice.

## Key findings

- B. atrox venom causes hypercalcemia and reduced bone calcium and phosphorus levels.
- Venom exposure increases oxidative stress and depletes antioxidants in bone tissue.
- Histology and SEM show significant trabecular bone thinning and structural damage.

## Abstract

Bothrops atrox is a terrestrial pit viper inhabiting the Amazon region. The venom of B. atrox acts almost immediately at the site of the bite, leading to significant tissue damage, but also affects different organs. The present study investigated the acute impact of intraperitoneally administered B. atrox venom on bone tissue integrity and calcium homeostasis in mice. Plasma, bone homogenate, and urine samples from adult male and female Swiss mice (30 ± 2 g/mouse) were analyzed to assess calcium and phosphorus levels. Additionally, we examined bone oxidative stress parameters alongside histological and scanning electron microscopy (SEM) analysis. Our findings showed that B. atrox envenoming results in profound phosphocalcic homeostasis disturbances with hypercalcemia, hypophosphatemia, and decreased calcium and phosphorus bone content. We also observed increased reactive oxygen species and malondialdehyde, and consumption of antioxidants. Histological examination and SEM of bone tissue revealed thinning and discontinuity of trabecular bone and a significant reduction in intertrabecular links. In conclusion, B. atrox envenoming profoundly impacts bone metabolism and structural integrity in mice. The venom induces substantial alterations in calcium and phosphorus homeostasis, elevates oxidative stress, and disrupts the antioxidant defense system. Histological and SEM analyses reveal extensive damage to the trabecular bone architecture, reinforcing the harmful effects of the venom on skeletal health. These results underscore the need for further research to better understand the acute and long-term implications of B. atrox envenoming, particularly regarding its potential impact on human bone.

Image 1

•Research into Bothrops atrox venom effect on bone remodeling, and calcium and phosphate homeostasis remain limited.•B. atrox venom induced significantly increase in plasma calcium levels.•B. atrox venom significantly reduced calcium and phosphorus levels in bone mice.•B. atrox venom induces stress homeostasis disorders in bone tissues in mice.•B.
atrox envenoming caused bone rarefaction confirmed by histology and scanning electron microscopy analysis.

Research into Bothrops atrox venom effect on bone remodeling, and calcium and phosphate homeostasis remain limited.

B. atrox venom induced significantly increase in plasma calcium levels.

B. atrox venom significantly reduced calcium and phosphorus levels in bone mice.

B. atrox venom induces stress homeostasis disorders in bone tissues in mice.

B.
atrox envenoming caused bone rarefaction confirmed by histology and scanning electron microscopy analysis.

## Linked entities

- **Species:** Bothrops atrox (taxon 8725), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** hypercalcemia (MESH:D006934), hypophosphatemia (MESH:D017674)
- **Chemicals:** reactive oxygen species (MESH:D017382), calcium (MESH:D002118), malondialdehyde (MESH:D008315), phosphorus (MESH:D010758)
- **Species:** Bothrops atrox (barba amarilla, species) [taxon 8725], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12769796/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12769796/full.md

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Source: https://tomesphere.com/paper/PMC12769796