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Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure on bone material properties
Authors:Mikko AJ Finnilä  Peter Zioupos  Maria Herlin  Hanna M Miettinen  Ulla Simanainen  Helen Håkansson  Juha Tuukkanen  Matti Viluksela  Timo Jämsä
Institution:1. Laboratoire de simulation et de modélisation du mouvement, Département de kinésiologie, Université de Montréal, 1700, rue Jacques Tétreault, Laval, QC H7N 0B6, Canada;2. École Polytechnique de Montréal, 6079, Succursale, Centre Ville, Montréal, QC H3C 3A7, Canada;3. Karolinska Institute, Stockholm, Sweden;4. The Swedish School of Sport and Health Sciences, Stockholm, Sweden;1. Department of Emergency Medicine, University of Iowa Carver College of Medicine, Iowa City, IA;2. Division of Critical Care, Department of Anesthesia, University of Iowa Carver College of Medicine, Iowa City, IA;3. Department of Surgery, University of Iowa Carver College of Medicine, Iowa City, IA;4. Department of Pharmaceutical Services, University of Iowa Hospitals and Clinics, Iowa City, IA;5. Department of Anesthesia, University of Iowa Carver College of Medicine, Iowa City, IA;1. Samaritano Hospital, Cardiology Department, Rua Bambina 98, Botafogo, Rio de Janeiro, RJ 22251-050, Brazil;2. Federal University of Rio de Janeiro, Edson Saad Heart Institute, Rua Rodolpho Paulo Rocco 255, Ilha do Fundão, Rio de Janeiro, RJ 21941-913, Brazil
Abstract:Dioxins are known to decrease bone strength, architecture and density. However, their detailed effects on bone material properties are unknown. Here we used nanoindentation methods to characterize the effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on nanomechanical behaviour of bone matrix.Pregnant rats were treated with a single intragastric dose of TCDD (1 μg/kg) or vehicle on gestational day 11. Tibias of female offspring were sampled on postnatal day (PND) 35 or 70, scanned at mid-diaphysis with pQCT, and evaluated by three-point bending and nanoindentation.TCDD treatment decreased bone mineralization (p<0.05), tibial length (p<0.01), cross-sectional geometry (p<0.05) and bending strength (p<0.05). Controls showed normal maturation pattern between PND 35 and 70 with decreased plasticity by 5.3% and increased dynamic hardness, storage and complex moduli by 26%, 13% and 12% respectively (p<0.05), while similar maturation was not observed in TCDD-exposed pups.In conclusion, for the first time, we demonstrate retardation of bone matrix maturation process in TCDD-exposed animals. In addition, the study confirms that developmental TCDD exposure has adverse effects on bone size, strength and mineralization. The current results in conjunction with macromechanical behaviour suggest that reduced bone strength caused by TCDD is more associated with the mineralization and altered geometry of bones than with changes at the bone matrix level.
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