Abstract

BackgroundExposure to cadmium (Cd) is considered a risk factor for various bone diseases in humans and experimental animals. This study investigated the acute effects of Cd on femoral bone structure of adult male rats after a single intraperitoneal administration.MethodsTen 4-month-old male Wistar rats were injected intraperitoneally with a single dose of 2 mg CdCl2/kg body weight and killed 36 h after the Cd had been injected. Ten 4-month-old males served as a control group. Differences in body weight, femoral weight, femoral length and histological structure of the femur were evaluated between the two groups of rats. The unpaired Student's t-test was used for establishment of statistical significance.ResultsA single intraperitoneal administration of Cd had no significant effect on the body weight, femoral weight or femoral length. On the other hand, histological changes were significant. Rats exposed to Cd had significantly higher values of area, perimeter, maximum and minimum diameters of the primary osteons' vascular canals and Haversian canals. In contrast, a significant decrease in all variables of the secondary osteons was observed in these rats.ConclusionsThe results indicate that, as expected, a single intraperitoneal administration of 2 mg CdCl2/kg body weight had no impact on macroscopic structure of rat's femora; however, it affected the size of vascular canals of primary osteons, Haversian canals, and secondary osteons.

Highlights

  • Exposure to cadmium (Cd) is considered a risk factor for various bone diseases in humans and experimental animals

  • Primary vascular radial bone tissue created branching or non-branching vascular canals radiating from the marrow cavity

  • Dense Haversian bone tissue characterized by dense concentration of secondary osteons was not observed in rats from either group

Read more

Summary

Introduction

Exposure to cadmium (Cd) is considered a risk factor for various bone diseases in humans and experimental animals. Cadmium (Cd) is considered a dangerous poison for humans and animals. The kidneys, liver, bones, and respiratory and cardiovascular systems are the most important target organs for Cd toxicity [3]. Changes in bone such as osteopenia, osteoporosis, and osteomalacia, with increased bone fragility and pathological fractures have been noted in humans and experimental animals as a result of exposure to Cd [4,5,6,7,8,9]. Bone toxicity of Cd can be modulated by both

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call