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Pathophysiologic studies of calves given 3-methylindole intraruminally
American Journal of Veterinary Research
|April 1, 1979
Summary
Young calves showed mild respiratory signs and lung lesions after 3-methylindole (3MI) administration. Cardiopulmonary function was only slightly affected, suggesting calves are more resistant to 3MI pulmonary toxicity than adult cattle.
Area of Science:
- Veterinary Toxicology
- Pulmonary Pathology
- Ruminant Physiology
Background:
- 3-methylindole (3MI), a toxic metabolite of tryptophan, is known to cause lung disease in cattle.
- Understanding the dose-response relationship and species-specific effects of 3MI is crucial for animal health.
- Young calves may exhibit different sensitivities to toxic insults compared to adult animals.
Purpose of the Study:
- To evaluate the clinical, cardiopulmonary, and pathological effects of intraruminal 3-methylindole (3MI) administration in young calves.
- To compare the susceptibility of young calves to 3MI-induced pulmonary toxicity with that of adult cattle.
Main Methods:
- Seven young calves were administered 0.25 g of 3-methylindole (3MI)/kg body weight intraruminally.
- Clinical signs, blood gas analysis, and cardiopulmonary parameters were monitored postadministration.
- Necropsy and histopathological examination of lungs and liver were performed.
Main Results:
- Mild respiratory signs and lesions were observed, with transient moderate depression and altered respiratory rate.
- Statistically significant changes in blood gases included decreased aortic oxygen tension and increased venous oxygen tension.
- Histopathology revealed thickened alveolar septae, interstitial lesions, alveolar epithelial changes, and scattered hepatocyte degeneration.
Conclusions:
- Young calves exhibit a degree of resistance to the pulmonary cytotoxic effects of 3-methylindole (3MI) compared to adult cattle.
- The observed lesions suggest 3MI induces interstitial pneumonia and associated edema and cellular infiltration in calves.
- Further research is warranted to elucidate the mechanisms of 3MI toxicity and potential species-specific differences.