Comparative angiotoxic responses of avian and rodent species in vivo: Implications in atherogenesis
- 1 April 1990
- journal article
- research article
- Published by Taylor & Francis in Journal of Toxicology and Environmental Health
- Vol. 29 (4) , 357-376
- https://doi.org/10.1080/15287399009531398
Abstract
As the intrinsic susceptibility to atherosclerosis differs among several taxonomic groups, the present studies were conducted to compare the angiotoxic responses of atherosclerosis‐susceptible (quail) and ‐resistant (rat) animals to allylamine, a selective cardiovascular toxin. Japanese quail (125–150 g) and Sprague‐Dawley rats (175–200 g) were gavaged daily for 1, 7, or 20 d with allylamine HCI (0.7, 7, and 70 mg/kg) or tap water. At the ultrastructural level, subchronic exposure of quail and rats to allylamine was associated with dose‐ and time‐dependent disruption of the structural integrity of aortas. These alterations correlated with fluctuations in the nonprotein thiol content of avian and rodent vessels. Angiotoxicity was not associated with alterations in serum cholesterol content. At all times and doses tested, quail were more susceptible than rats to the angiotoxic effects of allylamine. Although the avian sensitivity to toxic insult was greater than that of rodents, quail aortic homogenates bioactivated allylamine to a lesser extent than rat homogenates. Collectively, these results suggest that the aortic sensitivity to toxic insult in avian and rodent species correlates with their intrinsic susceptibility to vascular injury.This publication has 29 references indexed in Scilit:
- In vivo metabolism of the cardiovascular toxin, allylamineBiochemical Pharmacology, 1987
- Effects of long term consumption of fish oil (Maxepa®) on serum lipids and arterial ultrastructure in Japanese quail (Coturnix coturnix japonica)Atherosclerosis, 1987
- Cytocontractile structures and proteins of smooth muscle cells during the formation of experimental lesionsExperimental and Molecular Pathology, 1987
- Allylamine cardiovascular toxicity: V. tissue distribution and toxicokinetics after oral administrationToxicology, 1985
- Animal models in atherosclerosis researchExperimental and Molecular Pathology, 1985
- Herpesviridae in the endothelial and smooth muscle cells of the proximal aorta in arteriosclerotic patientsExperimental and Molecular Pathology, 1984
- Further investigations of the capacity of polynuclear aromatic hydrocarbons to elicit atherosclerotic lesionsJournal of Toxicology and Environmental Health, 1981
- Metabolism of benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene in chicken aortas: Monooxygenation, bioactivation to mutagens, and covalent binding to DNA in vitroToxicology and Applied Pharmacology, 1980
- Evidence for a Monoclonal Origin of Human Atherosclerotic PlaquesProceedings of the National Academy of Sciences, 1973
- The Toxicity of AllylaminesArchives of environmental health, 1960