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Gadolinium chloride toxicity in the mouse
A Spencer1, S Wilson, E Harpur
1Sanofi Research Division, Alnwick Research Centre, Northumberland, UK.
Human & Experimental Toxicology
|December 29, 1998
Summary
Gadolinium chloride causes dose-related toxicity in mice, including organ damage and mineral deposition. These findings are crucial for assessing the safety of gadolinium-based contrast agents in medical imaging.
Area of Science:
- Toxicology
- Biomedical Sciences
- Pharmacology
Background:
- Gadolinium-containing compounds are widely used as contrast agents in Magnetic Resonance Imaging (MRI).
- Understanding the toxicological profile of gadolinium is essential for ensuring patient safety.
- Previous studies have indicated potential toxic effects of gadolinium compounds.
Purpose of the Study:
- To evaluate the toxicological effects of a single intravenous injection of gadolinium chloride in CD-1 mice.
- To establish a dose-response relationship for gadolinium chloride toxicity.
- To inform the safety assessment of gadolinium-based contrast agents.
Main Methods:
- Groups of male and female CD-1 mice were administered single intravenous doses of gadolinium chloride (0, 0.05, 0.1, 0.2 mmol/kg).
- Animals were necropsied 48 hours post-dose for plasma analysis and histopathological examination.
- Biochemical markers of organ damage and tissue lesions were assessed.
Main Results:
- Elevated plasma levels of lactate dehydrogenase, aspartate aminotransferase, and alanine aminotransferase were observed at higher doses.
- Cholesterol and globulin levels were altered in a dose-dependent manner.
- Histological examination revealed dose-related lesions including mineral emboli, hepatocellular necrosis, and splenic abnormalities.
Conclusions:
- Gadolinium chloride induces significant, dose-dependent toxicological effects in mice.
- Observed lesions, including mineral deposition and organ damage, highlight potential risks.
- These findings underscore the importance of careful toxicological evaluation for gadolinium-based contrast agents in MRI.